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Items 1 to 100 of about 14013
1. Bittel DC, Kibiryeva N, O'Brien JE, Lofland GK, Butler MG: Gene expression in pediatric heart disease with emphasis on conotruncal defects. Prog Pediatr Cardiol; 2005 Jul;20(2):127-141

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • We report our microarray analysis showing over- and underexpression of individual genes and gene network interactions from dysplastic pulmonic tissue from two infants with tetralogy of Fallot compared with normal pulmonic tissue from an unaffected control infant.

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  • [Cites] Nature. 1995 Apr 13;374(6523):640-3 [7715703.001]
  • [Cites] Br Heart J. 1978 May;40(5):500-9 [656215.001]
  • [Cites] DNA Res. 2002 Apr 30;9(2):35-45 [12056413.001]
  • [Cites] J Thorac Cardiovasc Surg. 2004 Mar;127(3):746-54 [15001903.001]
  • [Cites] Science. 1995 Mar 24;267(5205):1831-4 [7892609.001]
  • [Cites] Proc Natl Acad Sci U S A. 2002 Aug 6;99(16):10488-93 [12149478.001]
  • [Cites] Circulation. 2003 May 20;107(19):2467-74 [12742993.001]
  • [Cites] Cell. 2001 Feb 23;104(4):619-29 [11239417.001]
  • [Cites] Nature. 2003 Oct 9;425(6958):633-7 [14534590.001]
  • [Cites] Gene. 2001 Jun 27;271(2):183-92 [11418239.001]
  • [Cites] J Mol Cell Cardiol. 2001 Oct;33(10):1879-86 [11603929.001]
  • [Cites] Curr Biol. 2002 Sep 17;12 (18):1605-10 [12372254.001]
  • [Cites] Cardiovasc Res. 2000 May;46(2):332-45 [10773238.001]
  • [Cites] Science. 1999 May 28;284(5419):1534-7 [10348742.001]
  • [Cites] Hum Mol Genet. 1999 Dec;8(13):2443-9 [10556292.001]
  • [Cites] Rev Esp Cardiol. 2002 Sep;55(9):962-74 [12236926.001]
  • [Cites] Hum Mutat. 2002 Oct;20(4):298-304 [12325025.001]
  • [Cites] J Med Genet. 2002 Aug;39(8):571-4 [12161596.001]
  • [Cites] Cardiovasc Pathol. 2000 Nov-Dec;9(6):303-15 [11146300.001]
  • [Cites] J Med Genet. 2002 Nov;39(11):807-11 [12414819.001]
  • [Cites] Nat Genet. 2001 Dec;29(4):465-8 [11704759.001]
  • [Cites] Nat Genet. 1999 Dec;23(4):387-8 [10581018.001]
  • [Cites] J Cardiovasc Electrophysiol. 2001 Nov;12(11):1223-9 [11761407.001]
  • [Cites] Physiol Genomics. 2002 Dec 26;12(1):53-60 [12502795.001]
  • [Cites] J Clin Invest. 1998 Feb 15;101(4):755-60 [9466969.001]
  • [Cites] Genet Test. 1999;3(2):157-72 [10464664.001]
  • [Cites] Circ Res. 1998 Feb 23;82(3):360-6 [9486664.001]
  • [Cites] Pediatr Surg Int. 2000;16(4):243-6 [10898222.001]
  • [Cites] Hum Mol Genet. 2001 Sep 1;10(18):1983-94 [11555635.001]
  • [Cites] J Biol Chem. 2000 Nov 10;275(45):35291-6 [10948187.001]
  • [Cites] Development. 2002 Oct;129(20):4685-96 [12361961.001]
  • [Cites] Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):8880-5 [12072561.001]
  • [Cites] Am J Hum Genet. 1998 Jun;62(6):1361-9 [9585603.001]
  • [Cites] Hum Mutat. 2001 Feb;17 (2):151-2 [11180599.001]
  • [Cites] Hum Mol Genet. 2002 Apr 15;11(8):915-22 [11971873.001]
  • [Cites] Nat Genet. 1997 Jul;16(3):243-51 [9207788.001]
  • [Cites] Development. 2002 Dec;129(24):5827-38 [12421720.001]
  • [Cites] Biochem Biophys Res Commun. 2001 Feb 2;280(4):964-9 [11162619.001]
  • [Cites] Dev Biol. 2001 Jul 1;235(1):62-73 [11412027.001]
  • [Cites] Biochem Biophys Res Commun. 2002 Oct 4;297(4):870-5 [12359233.001]
  • [Cites] Semin Perinatol. 1996 Dec;20(6):465-72 [9090774.001]
  • [Cites] J Clin Invest. 2002 Jul;110(2):177-84 [12122109.001]
  • [Cites] J Hum Genet. 2001;46(10):604-8 [11589220.001]
  • [Cites] Am J Med Genet. 2000 Winter;97(4):297-303 [11376441.001]
  • [Cites] Circulation. 2002 Nov 12;106(20):2567-74 [12427653.001]
  • (PMID = 28529438.001).
  • [ISSN] 1058-9813
  • [Journal-full-title] Progress in pediatric cardiology
  • [ISO-abbreviation] Prog. Pediatr. Cardiol.
  • [Language] eng
  • [Grant] United States / NCRR NIH HHS / RR / U54 RR019478
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
  • [Keywords] NOTNLM ; Cardiac development / Congenital heart defects / Conotruncal defects / Gene expression / Microarray / Pediatric cardiology
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2. Ginsberg G: Endoluminal Therapies for Barrett's Esophagus and Dysplasia. Gastroenterol Hepatol (N Y); 2006 Mar;2(3):165-167

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endoluminal Therapies for Barrett's Esophagus and Dysplasia.

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  • [Cites] Gastroenterology. 2000 Apr;118(4):670-7 [10734018.001]
  • [Cites] Gastrointest Endosc. 2005 Oct;62(4):488-98 [16185958.001]
  • [Cites] Gastrointest Endosc. 2001 Dec;54(6):682-8 [11726842.001]
  • [Cites] Clin Gastroenterol Hepatol. 2003 Jul;1(4):241-5 [15017662.001]
  • [Cites] Clin Gastroenterol Hepatol. 2003 Jul;1(4):258-63 [15017666.001]
  • [Cites] Gastroenterology. 2001 Jun;120(7):1607-19 [11375943.001]
  • (PMID = 28286444.001).
  • [ISSN] 1554-7914
  • [Journal-full-title] Gastroenterology & hepatology
  • [ISO-abbreviation] Gastroenterol Hepatol (N Y)
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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3. Lücke T, Pape L: Disseminated cutaneous papillomas in Schimke immuno-osseous dysplasia. NDT Plus; 2008 Feb;1(1):49-50

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Disseminated cutaneous papillomas in Schimke immuno-osseous dysplasia.

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  • [Cites] Eur J Pediatr. 2000 Jan-Feb;159(1-2):1-7 [10653321.001]
  • [Cites] Pediatr Nephrol. 1990 Mar;4(2):117-21 [2397176.001]
  • [Cites] Clin Nephrol. 1995 Feb;43(2):89-95 [7736684.001]
  • (PMID = 28656993.001).
  • [ISSN] 1753-0784
  • [Journal-full-title] NDT plus
  • [ISO-abbreviation] NDT Plus
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Keywords] NOTNLM ; Schimke / kidney transplantation / papilloma
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4. Pommier S, Chazalon E, Roux L, Meyer F: [Acute blepharoptosis caused by fibrous dysplasia]. J Fr Ophtalmol; 2008 Jun;31(6 Pt 1):623
Genetic Alliance. consumer health - Fibrous Dysplasia.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Acute blepharoptosis caused by fibrous dysplasia].
  • [Transliterated title] Ptôsis aigu unilatéral révélant une dysplasie fibreuse.
  • We report a case of fibrous dysplasia revealed by acute ptosis in a 38-year-old patient.
  • Given this acute presentation, emergency cerebral imagery was carried out, providing a diagnosis of fibrous dysplasia with orbital and cavernous repercussions, with no sign of cerebral disorder or obvious vascular lesion.
  • Fibrous dysplasia is a rare pathology but presents varied clinical presentations.
  • [MeSH-major] Blepharoptosis / etiology. Fibrous Dysplasia, Polyostotic / complications. Frontal Bone / pathology. Orbital Diseases / complications. Sphenoid Bone / pathology

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  • (PMID = 18772816.001).
  • [ISSN] 1773-0597
  • [Journal-full-title] Journal français d'ophtalmologie
  • [ISO-abbreviation] J Fr Ophtalmol
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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5. Rastogi A, Sharma P: Short-Segment Barrett's Esophagus and Adenocarcinoma. Gastroenterol Hepatol (N Y); 2006 Feb;2(2):134-139

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Studies have shown that although the prevalence of short-segment Barrett's esophagus is higher than that of long-segment Barrett's esophagus, the risk of developing dysplasia and adenocarcinoma may actually be lower in those patients with short segment Barrett's esophagus.
  • Nonetheless, both dysplasia and esophageal adenocarcinoma have been reported in patients with short-segment Barrett's esophagus, making this arbitrary distinction clinically unimportant.

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  • [Cites] Gut. 1992 Jun;33(6):733-7 [1624150.001]
  • [Cites] J Natl Cancer Inst. 2005 Jan 19;97(2):142-6 [15657344.001]
  • [Cites] Gastroenterology. 1984 Oct;87(4):927-33 [6468881.001]
  • [Cites] Am J Gastroenterol. 1999 Dec;94(12):3413-9 [10606296.001]
  • [Cites] JAMA. 1993 Sep 15;270(11):1320 [8360967.001]
  • [Cites] Gut. 2003 Jan;52(1):24-7 [12477754.001]
  • [Cites] Gastroenterology. 1995 Nov;109(5):1541-6 [7557137.001]
  • [Cites] Am J Gastroenterol. 1997 Mar;92(3):414-8 [9068460.001]
  • [Cites] Dig Dis Sci. 2002 Sep;47(9):2108-11 [12353864.001]
  • [Cites] Gastroenterology. 1999 Feb;116(2):277-85 [9922307.001]
  • [Cites] Gastroenterology. 1989 May;96(5 Pt 1):1249-56 [2703113.001]
  • [Cites] Gastrointest Endosc. 2001 May;53(6):559-65 [11323579.001]
  • [Cites] Gastrointest Endosc. 1987 Dec;33(6):413-6 [3443258.001]
  • [Cites] Cancer. 1987 Sep 1;60(5):1094-8 [3607726.001]
  • [Cites] Am J Gastroenterol. 2002 Aug;97(8):1888-95 [12190150.001]
  • [Cites] Gastroenterology. 2003 Dec;125(6):1670-7 [14724819.001]
  • [Cites] Am J Gastroenterol. 1999 Apr;94(4):913-8 [10201456.001]
  • [Cites] Am J Gastroenterol. 2001 May;96(5):1378-82 [11374671.001]
  • [Cites] Gut. 1997 Nov;41(5):585-9 [9414961.001]
  • [Cites] Endoscopy. 1993 Nov;25(9):652-4 [8119225.001]
  • [Cites] Am J Gastroenterol. 2002 Aug;97(8):1930-6 [12190156.001]
  • [Cites] Ann Intern Med. 2000 Apr 18;132(8):612-20 [10766679.001]
  • [Cites] Dig Dis Sci. 1997 Mar;42(3):597-602 [9073145.001]
  • [Cites] N Engl J Med. 1986 Aug 7;315(6):362-71 [2874485.001]
  • [Cites] Gastroenterology. 2004 Jul;127(1):310-30 [15236196.001]
  • [Cites] J Gastroenterol. 2004 Jan;39(1):14-20 [14767729.001]
  • [Cites] Ann Surg. 1983 Oct;198(4):554-65 [6625723.001]
  • [Cites] Gut. 1997 Jun;40(6):710-5 [9245922.001]
  • [Cites] Am J Surg Pathol. 2001 Jan;25(1):87-94 [11145256.001]
  • [Cites] Lancet. 1994 Dec 3;344(8936):1533-6 [7983953.001]
  • [Cites] Gastroenterology. 2002 Aug;123(2):461-7 [12145799.001]
  • [Cites] Gut. 1996 Jul;39(1):5-8 [8881798.001]
  • [Cites] Am J Gastroenterol. 1996 Aug;91(8):1507-11 [8759651.001]
  • [Cites] Gut. 2000 Jan;46(1):9-13 [10601047.001]
  • [Cites] Hum Pathol. 1988 Aug;19(8):942-8 [3402983.001]
  • [Cites] Gastrointest Endosc. 1994 Jan-Feb;40(1):111 [8163114.001]
  • [Cites] Gut. 1998 Jul;43(1):17-21 [9771400.001]
  • [Cites] Gut. 1991 Dec;32(12):1441-6 [1773946.001]
  • [Cites] Gastrointest Endosc. 2001 Sep;54(3):289-93 [11522967.001]
  • [Cites] Dig Dis Sci. 1997 Mar;42(3):603-7 [9073146.001]
  • [Cites] Dig Dis Sci. 1992 Jan;37(1):137-43 [1728519.001]
  • [Cites] Br J Surg. 1988 Aug;75(8):760-3 [3167523.001]
  • [Cites] Am J Gastroenterol. 1994 May;89(5):670-80 [8172136.001]
  • [Cites] Gastrointest Endosc. 2005 Feb;61(2):226-31 [15729230.001]
  • [Cites] Cancer. 1993 Aug 15;72(4):1155-8 [8339208.001]
  • [Cites] Am J Gastroenterol. 1996 May;91(5):981-6 [8633592.001]
  • [Cites] Am J Gastroenterol. 1997 Nov;92(11):2012-6 [9362182.001]
  • [Cites] Am J Gastroenterol. 1997 Mar;92(3):407-13 [9068459.001]
  • [Cites] Histopathology. 2001 Apr;38(4):307-11 [11318895.001]
  • [Cites] Gut. 1998 May;42(5):659-62 [9659160.001]
  • [Cites] Am J Gastroenterol. 1998 Jul;93(7):1033-6 [9672325.001]
  • [Cites] Cancer. 1996 Oct 15;78(8):1820-8 [8859198.001]
  • [Cites] Am J Gastroenterol. 1999 Aug;94(8):2037-42 [10445525.001]
  • [Cites] Am J Gastroenterol. 2000 Aug;95(8):1888-93 [10950031.001]
  • [Cites] Gastroenterology. 1993 Feb;104(2):510-3 [8425693.001]
  • [Cites] Gastrointest Endosc. 2001 Sep;54(3):294-301 [11522968.001]
  • [Cites] Am J Gastroenterol. 1999 Apr;94(4):937-43 [10201460.001]
  • [Cites] Cancer. 1998 Nov 15;83(10):2049-53 [9827707.001]
  • [Cites] N Engl J Med. 1985 Oct 3;313(14):857-9 [4033716.001]
  • (PMID = 28286441.001).
  • [ISSN] 1554-7914
  • [Journal-full-title] Gastroenterology & hepatology
  • [ISO-abbreviation] Gastroenterol Hepatol (N Y)
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Keywords] NOTNLM ; Barrett’s esophagus / adenocarcinoma / high-grade dysplasia / long-segment Barrett’s esophagus / low-grade dysplasia / short-segment Barrett’s esophagus
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6. Allali J, Roche O, Monnet D, Brezin A, Renard G, Dufier JL: [Anhidrotic ectodermal dysplasia: "congenital ameibomia"]. J Fr Ophtalmol; 2007 May;30(5):525-8
Genetic Alliance. consumer health - Ectodermal Dysplasia Anhidrotic.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Anhidrotic ectodermal dysplasia: "congenital ameibomia"].
  • [Transliterated title] Dysplasie ectodermique anhidrotique: "l'ameibomie congénitale".
  • Anhidrotic ectodermal dysplasia is a congenital, generally X-linked dermatosis that associates facial dysmorphy, short stature, and severe blepharitis.
  • The anomalies of the skin are epidermic abnormalities; reduction of the glands of the derm, particularly the sweat glands, explaining the hypohidrosis; onychodysplasia; trichodysplasia; and abnormal dentition.
  • [MeSH-major] Ectodermal Dysplasia 1, Anhidrotic / diagnosis. Eye Abnormalities / diagnosis. Lacrimal Apparatus / abnormalities

  • Genetic Alliance. consumer health - Ectodermal Dysplasia.
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  • (PMID = 17568347.001).
  • [ISSN] 1773-0597
  • [Journal-full-title] Journal français d'ophtalmologie
  • [ISO-abbreviation] J Fr Ophtalmol
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
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7. Ullman TA: Low-Grade Colorectal Dysplasia and the Need for Colectomy. Gastroenterol Hepatol (N Y); 2006 Dec;2(12):868-870

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Low-Grade Colorectal Dysplasia and the Need for Colectomy.

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  • [Cites] Gastroenterology. 2004 Feb;126(2):451-9 [14762782.001]
  • [Cites] Gastroenterology. 1994 Oct;107(4):934-44 [7926483.001]
  • [Cites] Am J Gastroenterol. 1995 Dec;90(12):2106-14 [8540497.001]
  • [Cites] Dis Colon Rectum. 2002 May;45(5):615-20 [12004210.001]
  • [Cites] Gut. 2004 Feb;53(2):256-60 [14724160.001]
  • [Cites] Gastroenterology. 2003 Apr;124(4):880-8 [12671882.001]
  • [Cites] Lancet. 1994 Jan 8;343(8889):71-4 [7903776.001]
  • [Cites] Gut. 2003 Aug;52(8):1127-32 [12865270.001]
  • [Cites] Gastroenterology. 1999 Dec;117(6):1288-94; discussion 1488-91 [10579969.001]
  • [Cites] Gastroenterology. 2003 Nov;125(5):1311-9 [14598247.001]
  • [Cites] Am J Gastroenterol. 2002 Apr;97(4):922-7 [12008669.001]
  • [Cites] Hum Pathol. 1983 Nov;14 (11):931-68 [6629368.001]
  • [Cites] Gastroenterology. 1999 Dec;117(6):1295-300 [10579970.001]
  • (PMID = 28331477.001).
  • [ISSN] 1554-7914
  • [Journal-full-title] Gastroenterology & hepatology
  • [ISO-abbreviation] Gastroenterol Hepatol (N Y)
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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8. Vlatis G, Georgiades G, Magnissalis EA, Hartofilakidis G: Mid-term behaviour of cemented titanium stems: A seven to eleven year clinical. Hip Int; 2005 Jan - Mar;15(1):12-20

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • In most of them (23 hips) the pre-operative diagnosis was hip dysplasia or dislocation.

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  • (PMID = 28224577.001).
  • [ISSN] 1724-6067
  • [Journal-full-title] Hip international : the journal of clinical and experimental research on hip pathology and therapy
  • [ISO-abbreviation] Hip Int
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Italy
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9. DAngelo F, Molina M, Giudici M, Cherubino P: Radiographic evaluation of the hip rotation centre after total joint replacement in hip dysplasia. Hip Int; 2005 Apr - Jun;15(2):92-97

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Radiographic evaluation of the hip rotation centre after total joint replacement in hip dysplasia.
  • : A retrospective study was conducted to correlate the clinical result of joint replacement in dysplastic hips with the obtained modifications of the rotation centre.
  • Sixty primary total hip arthroplasties were performed on 46 patients suffering from hip dysplasia at our institution.

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  • (PMID = 28224574.001).
  • [ISSN] 1724-6067
  • [Journal-full-title] Hip international : the journal of clinical and experimental research on hip pathology and therapy
  • [ISO-abbreviation] Hip Int
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Italy
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10. Shah NG, Trivedi TI, Tankshali RA, Goswami JA, Shah JS, Jetly DH, Kobawala TP, Patel KC, Shukla SN, Shah PM, Verma RJ: Molecular alterations in oral carcinogenesis: significant risk predictors in malignant trasformation and tumor progression. Int J Biol Markers; 2007 Apr - Jun;22(2):132-143

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • For this purpose, EGFR, Stat3, H-ras, c-myc, p53, cyclin D1, p16, Rb, Ki-67 and Bcl-2 were localized immunohistochemically in normal mucosa (n=12), hyperplasia (n=35), dysplasia (n=25), early stage carcinoma (n=65) and advanced stage carcinoma (n=70).
  • Using multivariate logistic regression analysis, the significant risk predictor for hyperplasia from normal mucosa was Ki-67 (OR=5.75, p=0.021); the significant risk predictors for dysplasia from hyperplasia were EGFR (OR=12.96, p=0.002), Stat3 (OR=17.16, p=0.0001), p16 (OR=5.50, p=0.039) and c-myc (OR=5.99, p=0.052); the significant risk predictors for early stage carcinoma from dysplasia were p53 (OR=6.63, p=0.0001) and Rb (OR=3.81, p=0.056); and the significant risk predictors for further progression were EGFR (OR=5.50, p=0.0001), Stat3 (OR=4.49, p=0.0001), H-ras (OR=4.05, p=0.001) and c-myc (OR=2.99, p=0.015).
  • Gene products of the mitogenic signaling pathway play an equally significant role as cell cycle regulatory proteins in the hyperplasia-dysplasia-early-advanced-carcinoma sequence and together may provide a reference panel of markers for use in defining premalignant lesions and predicting the risk of malignant transformation and tumor progression.

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  • (PMID = 28207143.001).
  • [ISSN] 1724-6008
  • [Journal-full-title] The International journal of biological markers
  • [ISO-abbreviation] Int. J. Biol. Markers
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Italy
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11. Aslam N, Wainwright A, Benson MK: The false profile arthrogram in developmental dysplasia of the hip. Hip Int; 2005 Jul - Sep;15(3):177-181

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] The false profile arthrogram in developmental dysplasia of the hip.
  • : Arthrography is useful in the evaluation and treatment of developmental dysplasia of the hip.

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  • (PMID = 28224604.001).
  • [ISSN] 1724-6067
  • [Journal-full-title] Hip international : the journal of clinical and experimental research on hip pathology and therapy
  • [ISO-abbreviation] Hip Int
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Italy
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12. Rödl R, Götze C: [Fibrous dysplasia]. Orthopade; 2008 Jan;37(1):49-55
Genetic Alliance. consumer health - Fibrous Dysplasia.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Fibrous dysplasia].
  • [Transliterated title] Fibröse Dysplasie.
  • Fibrous dysplasia is a tumorlike, benign lesion, caused by sporadic mutation during early embryogenesis.
  • The skeletal involvement becomes increasingly visible during growth.
  • The number and extent of dysplastic lesions increase until the age of 15.
  • Malignant transformation of fibrous dysplastic lesions is less than 1%; therefore, treatment or resection of the lesion itself is not necessary.
  • The progress of the lesions during growth can lead to pain, fractures, and deformities.
  • [MeSH-major] Fibrous Dysplasia of Bone
  • [MeSH-minor] Adolescent. Arthroplasty, Replacement, Hip. Bone Density Conservation Agents / therapeutic use. Child, Preschool. Diphosphonates / therapeutic use. Facial Bones / radiography. Female. Fibrous Dysplasia, Polyostotic / radiography. Follow-Up Studies. Fracture Fixation, Internal. Fracture Healing. Fractures, Bone / etiology. Fractures, Bone / surgery. Hip Prosthesis. Humans. Infant. Male. Skull / radiography. Time Factors. Tomography, X-Ray Computed. Treatment Outcome

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  • (PMID = 18084739.001).
  • [ISSN] 0085-4530
  • [Journal-full-title] Der Orthopäde
  • [ISO-abbreviation] Orthopade
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Bone Density Conservation Agents; 0 / Diphosphonates
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13. Bakanay SM, Karakiliç E, Civriz-Bozdag S, Arat M, Ozcan M, Gurman G, Ilhan O, Beksac M, Konuk N, Arslan O: 5-azacytidine treatment results in myelodysplastic syndrome. J Clin Oncol; 2009 May 20;27(15_suppl):e18003

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • : e18003 Background: Myelodysplastic syndrome (MDS) is a clonal disease of hematopoiesis characterized by dysplasia in one or more series.

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  • (PMID = 27963997.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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14. Wilson KS: Regression of follicular lymphoma with alternative therapy using Devil's Claw (DC); Coincidence or causation? J Clin Oncol; 2009 May 20;27(15_suppl):e19560

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • In January 2000, pt #1 presented with co-existent IgG plasma cell dyscrasia and stage 3A grade 2 FL with 5 cm cervical and R/P nodes.

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  • (PMID = 27961063.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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15. Gray JE, Altiok S, Alexandrow M, Walsh F, Tockman M, Bepler G: Chemoprevention with enzastaurin: First-year results. J Clin Oncol; 2009 May 20;27(15_suppl):1520

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Eligibility includes age 45 or younger, smoking 30 or fewer packs per year, quit for less than one 1 year, and bronchial meta/dysplasia.
  • Three had normal histology at all sites, 16 had metaplasia, and two had dysplasia in at least one site (84% abnormal bronchial histology rate, 1 pending).

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  • (PMID = 27964343.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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16. Spadaro P, Ingemi M, Pitini V, Arrigo C, Soto Parra H: Myelodysplastic syndromes developing after imatinib therapy for GIST. J Clin Oncol; 2009 May 20;27(15_suppl):10532

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • METHODS: Between January 2007 and December 2008, bone marrow samples for morphologic analysis, FISH and classical cytogenetics were obtained from 49 pts. (30 male; 19 female, mean age 62) with unresectable or metastatic GIST before and during treatment with 400 mg/d of imatinib.
  • A trisomy 8 was detectable in seven pts. even if, curiously, in four of these pts. this come and went on repeated sampling without any apparent clinical effect, three pts. developed an MDS (two refractory cytopenias with multilineage dysplasia, and one refractory cytopenia with multilineage dysplasia and ringed sideroblast).

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  • (PMID = 27963910.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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17. Gold D, Modrak DE, Newsome G, Karanjawala Z, Hruban R, Goggins M, Goldenberg DM: Detection of early-stage pancreatic carcinoma. J Clin Oncol; 2009 May 20;27(15_suppl):4613

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Of interest, a difference in the labeling pattern was observed in association with the grade of dysplasia, providing easy identification of MCN with high- grade dysplasia.

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  • (PMID = 27964187.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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18. Calistri D, Rengucci C, Casadei-Gardini A, Scarpi E, Zoli W, Falcini F, Milandri C, Amadori D, Silvestrini R: FL-DNA approach for noninvasive early diagnosis of colorectal cancer in FOBT-screened patients. J Clin Oncol; 2009 May 20;27(15_suppl):11062

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • In particular, diagnostic accuracy was similar for lesions of any localization, level of dysplasia and histopathological characteristic, and higher for lesions > 2 cm and multiple lesions.

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  • (PMID = 27963138.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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19. Wenzel L, Chase D, Hawk J, Osann K, Tewari K: Predictors of compliance in colposcopy clinic follow-up among the uninsured. J Clin Oncol; 2009 May 20;27(15_suppl):e20511

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The no-show rate for follow-up appointments after HPV-related abnormal pap smears approximates 50% in high risk populations.
  • METHODS: A longitudinal cohort study was conducted by chart review for all patients identified as having had a colposcopy exam for HPV-associated cervical dysplasia at a southern California inner city clinic from 2006 to 2007.

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  • (PMID = 27960922.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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20. Kilpatrick MW, Jalali GR, Scamporino J, Menzin A, Tafas T, Walat R, Tsipouras P: Predictive value of gain of 3q for cervical dysplasia and potential utility in the clinical management of LSIL. J Clin Oncol; 2009 May 20;27(15_suppl):5583

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Predictive value of gain of 3q for cervical dysplasia and potential utility in the clinical management of LSIL.
  • Research demonstrates that the chromosome 3q26 region is found to be amplified in patients with cervical cancer and that the frequency of this 3q gain increases with dysplasia severity.
  • Of the 32 cases with tissue diagnosis, 11 women had progressed to CIN2+, of which 10 were FISH positive; and 18 of 21 women with tissue diagnosis of ≤CIN1 were FISH negative, for a sensitivity of 91% (95% CI of 59, 100), specificity of 86% (95% CI of 64, 97) and a negative predictive value of 95% (95% CI of 74, 100).

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  • (PMID = 27962394.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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21. Kulkarni ML, Matadh PS, Prabhu SP, Kulkarni PM: Fibrochondrogenesis. Indian J Pediatr; 2005 Apr;72(4):355-357

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Fibrochondrogenesis is a rare lethal short-limb skeletal dysplasia.

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  • (PMID = 28386830.001).
  • [ISSN] 0973-7693
  • [Journal-full-title] Indian journal of pediatrics
  • [ISO-abbreviation] Indian J Pediatr
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Keywords] NOTNLM ; Autosomal recessive / Fibrochondrogenesis / Lethal skeletal dysplasia
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22. Jajeh A: Reccurent and prolonged panctopenia with rituximab therapy. J Clin Oncol; 2009 May 20;27(15_suppl):e19550

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Whether, bone marrow aplasia, dysplasia or other immune mechanism exist need more study.

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  • (PMID = 27961092.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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23. Chen C, Campbell F, Patruno J, Kimmel S, Boulay R, Meyers C, Martino M: Factors associated with regression of cervical dysplasia in adolescents: A retrospective study. J Clin Oncol; 2009 May 20;27(15_suppl):5582

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Factors associated with regression of cervical dysplasia in adolescents: A retrospective study.
  • : 5582 Background: Sexually active adolescents have high rates of infection with human papilloma virus (HPV) and abnormal pap smears.
  • The aim of our study was to identify factors associated with regression of cervical dysplasia in adolescents.
  • METHODS: We identified adolescent patients (aged 12-21 years) who had abnormal pap smears at the Center for Women's Medicine at Lehigh Valley Hospital in Allentown, PA, by CPT code from a database between Jan 2004 and Dec 2006.
  • Chi-square analysis with logistic regression and multivariate analysis were used to identify factors associated with regression of cervical dysplasia.
  • On multivariate analysis, patients who did not smoke were significantly more likely to show regression of cervical dysplasia on pap smear than women who smoked (OR 2.17, 95% CI 1.03-4.55, p = 0.039).
  • Other factors were not statistically significant in predicting regression of cervical dysplasia.
  • CONCLUSIONS: Adolescents who smoke were more likely to have persistent cervical dysplasia than non-smoking adolescents, putting smokers at an increased risk of advanced disease.

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  • (PMID = 27962395.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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24. Haddad PA: Activity of bortezomib (B) in plasma cell dyscrasia (PCD) with POEMS-like syndrome. J Clin Oncol; 2009 May 20;27(15_suppl):e19564

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Activity of bortezomib (B) in plasma cell dyscrasia (PCD) with POEMS-like syndrome.

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  • (PMID = 27961060.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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25. Luketich J, Pennathur A, Catalano PJ, Swanson SJ, de Hoyos AL, Maddaus MA, Nguyen N, Benson AB 3rd, Fernando HC: Results of a phase II multicenter study of minimally invasive esophagectomy (Eastern Cooperative Oncology Group Study E2202). J Clin Oncol; 2009 May 20;27(15_suppl):4516

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Final pathology included high-grade dysplasia (n=11), and EAC (n=88).

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  • (PMID = 27962698.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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26. Wirth T: [Spondyloepiphyseal and metaphyseal dysplasia]. Orthopade; 2008 Jan;37(1):8-16
Genetic Alliance. consumer health - Spondyloepiphyseal dysplasia.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Spondyloepiphyseal and metaphyseal dysplasia].
  • [Transliterated title] Spondyloepiphysäre und metaphysäre Dysplasie.
  • Spondyloepiphyseal, metaphyseal and spondylometaphyseal dysplasias are a group of hereditary skeletal diseases, which lead to small stature, axial deformities of the lower extremities and spinal deformities.

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  • (PMID = 18210084.001).
  • [ISSN] 0085-4530
  • [Journal-full-title] Der Orthopäde
  • [ISO-abbreviation] Orthopade
  • [Language] ger
  • [Publication-type] Comparative Study; English Abstract; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 32
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27. Dämmrich TD, Knapp FB, Boedeker CC, Klenzner T, Berlis A, Maier W, Schipper J: [Craniofacial fibrous dysplasia: scan policy or surgery?]. Laryngorhinootologie; 2007 Mar;86(3):184-92
Genetic Alliance. consumer health - Fibrous Dysplasia.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Craniofacial fibrous dysplasia: scan policy or surgery?].
  • [Transliterated title] Kraniofaziale Fibröse Dysplasie: Observieren oder Operieren?
  • BACKGROUND: The aetiologic correlations of fibrous dysplasia (FD) are more and more decoded by molecular biology, improved imaging procedures, and the use of computer assisted surgery--thus a review of present diagnostics and therapy methods is evaluated.
  • [MeSH-major] Facial Bones. Fibrous Dysplasia of Bone. Frontal Bone. Skull Base

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  • (PMID = 17131258.001).
  • [ISSN] 0935-8943
  • [Journal-full-title] Laryngo- rhino- otologie
  • [ISO-abbreviation] Laryngorhinootologie
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 41
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28. Gurr A, Ebsen M, Blanke P, Stark T, Dazert S: [Treatment of fibrous dysplasia]. Laryngorhinootologie; 2007 Nov;86(11):781-4
Genetic Alliance. consumer health - Fibrous Dysplasia.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Treatment of fibrous dysplasia].
  • [Transliterated title] Therapiekonzepte bei fibröser Dysplasie.
  • BACKGROUND: The fibrous dysplasia is a rare disease of bone metabolism.
  • The patients suffer from problems such as cosmetical limitation, recurrent pain and in later phases from functional losses which result from bone dysplasia.
  • PATIENTS: The Department of Otorhinolaryngology in Bochum has been involved in the therapy of eight patients suffering from fibrous dysplasia which have been treated and examined from six to twenty years.
  • RESULTS: Treatment in fibrous dysplasia can be efficient in increasing quality of life.
  • CONCLUSIONS: The staged therapy of fibrous dysplasia consists of conservative and surgical treatment and the combination of both.
  • [MeSH-major] Fibrous Dysplasia of Bone / therapy. Skull Base

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  • (PMID = 17533586.001).
  • [ISSN] 0935-8943
  • [Journal-full-title] Laryngo- rhino- otologie
  • [ISO-abbreviation] Laryngorhinootologie
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
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29. La Batide Alanore A, Perdu J, Plouin PF: [Fibromuscular dysplasia]. Presse Med; 2007 Jun;36(6 Pt 2):1016-23
Genetic Alliance. consumer health - Fibromuscular Dysplasia.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Fibromuscular dysplasia].
  • [Transliterated title] Dysplasie fibromusculaire artérielle.
  • Fibromuscular dysplasia is an idiopathic, segmental, nonatherosclerotic and noninflammatory disease of the muscle layer of arterial walls that leads to stenosis of small- and medium-sized arteries.
  • Fibromuscular dysplasia preferentially affects young women.
  • Renal fibromuscular dysplasia can cause hypertension by stenosis of the renal artery, most often seen on angiography as resembling a "pearl necklace".
  • Cerebrovascular fibromuscular dysplasia becomes symptomatic when the arterial stenosis is tight and causes hypoperfusion, embolism, or thrombosis or when arterial dissection or rupture of the associated aneurysm occurs.
  • [MeSH-major] Fibromuscular Dysplasia / diagnosis

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  • (PMID = 17442534.001).
  • [ISSN] 0755-4982
  • [Journal-full-title] Presse medicale (Paris, France : 1983)
  • [ISO-abbreviation] Presse Med
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Number-of-references] 34
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30. Dembinski J, Kroll M, Lewin M, Winkler P: [Unilateral pulmonary agenesis, aplasia and dysplasia]. Z Geburtshilfe Neonatol; 2009 Apr;213(2):56-61

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Unilateral pulmonary agenesis, aplasia and dysplasia].
  • [Transliterated title] Unilaterale pulmonale Agenesie, Aplasie und Dysplasie.
  • In three term neonates the diagnoses of unilateral pulmonary agenesis, aplasia and dysplasia, respectively, were based on angiography, MRI and bronchoscopy.
  • A possible relationship to disrupted regulation of embryo-genetic factors such as T-BOX genes, PITX2 and growth factors ( FGF10), which regulate ASYMMETRICAL pulmonary morphogenesis is discussed.

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  • (PMID = 19319794.001).
  • [ISSN] 0948-2393
  • [Journal-full-title] Zeitschrift für Geburtshilfe und Neonatologie
  • [ISO-abbreviation] Z Geburtshilfe Neonatol
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 41
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31. Boisramé-Gastrin S, Zimmermann P, Blancard PS, Denhez F: [Mandibular fibrous dysplasia: a monostotic form]. Rev Stomatol Chir Maxillofac; 2008 Dec;109(6):383-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Mandibular fibrous dysplasia: a monostotic form].
  • [Transliterated title] Dysplasie fibreuse mandibulaire : une forme monostotique.
  • INTRODUCTION: The onset of one or several diastema in adults with no link of etiology to tooth loss or to a periodontal problem can be the first evocative sign of an acromegaly or a benign or malignant tumoral process.
  • The biopsy proved the diagnosis of fibrous dysplasia.
  • DISCUSSION: Etiologies of fibrous dysplasia are varied.
  • [MeSH-major] Diastema / etiology. Fibrous Dysplasia, Monostotic / complications. Mandibular Diseases / complications

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  • (PMID = 18951597.001).
  • [ISSN] 0035-1768
  • [Journal-full-title] Revue de stomatologie et de chirurgie maxillo-faciale
  • [ISO-abbreviation] Rev Stomatol Chir Maxillofac
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 7440-26-8 / Technetium
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32. Fotso J, Hugentobler M, Kiliaridis S, Richter M: [Anhidrotic ectodermal dysplasia. Rehabilitation]. Rev Stomatol Chir Maxillofac; 2009 Feb;110(1):50-4
Genetic Alliance. consumer health - Ectodermal Dysplasia Anhidrotic.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Anhidrotic ectodermal dysplasia. Rehabilitation].
  • [Transliterated title] Dysplasie ectodermique anhidrotique. Réhabilitation.
  • INTRODUCTION: Anhidrotic ectodermal dysplasia (EAD) is an inherited syndrome with an incidence of one per 100,000 live births and is characterized by hypotrichosis, anhidrosis or hypohidrosis, and oligodontia.
  • DISCUSSION: Dental implants are a reliable oral rehabilitation treatment for children presenting with ectodermal dysplasia.
  • [MeSH-major] Anodontia / rehabilitation. Dental Implantation, Endosseous. Dental Prosthesis, Implant-Supported. Diastema / therapy. Ectodermal Dysplasia / complications. Ectodermal Dysplasia / rehabilitation

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  • (PMID = 19155030.001).
  • [ISSN] 0035-1768
  • [Journal-full-title] Revue de stomatologie et de chirurgie maxillo-faciale
  • [ISO-abbreviation] Rev Stomatol Chir Maxillofac
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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33. Jäger M, Westhoff B, Zilkens C, Weimann-Stahlschmidt K, Krauspe R: [Indications and results of corrective pelvic osteotomies in developmental dysplasia of the hip]. Orthopade; 2008 Jun;37(6):556-70, 572-4, 576
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Indications and results of corrective pelvic osteotomies in developmental dysplasia of the hip].
  • [Transliterated title] Indikation und Ergebnisse hüftnaher Osteotomien bei Dysplasie.
  • Besides skeletal maturity and tissue quality at the time of surgery, the kind and degree of deformity, the causative pathologies in secondary dysplasias, and the prognosis have to be considered when deciding for or against a surgical procedure.
  • Developmental dysplasia of the hip (DDH) is the most frequent deformity that indicates reorienting surgery on the hip joint in children and adolescents.
  • When the triradiate cartilage (growth plate) is closed, good outcomes can be achieved by the Ganz osteotomy.

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  • (PMID = 18493740.001).
  • [ISSN] 0085-4530
  • [Journal-full-title] Der Orthopäde
  • [ISO-abbreviation] Orthopade
  • [Language] ger
  • [Publication-type] Comparative Study; English Abstract; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 160
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34. Lücke T, Kanzelmeyer N, Franke D, Hartmann H, Ehrich JH, Das AM: [Schimke immuno-osseous dysplasia. A pediatric disease reaches adulthood]. Med Klin (Munich); 2006 Mar 15;101(3):208-11

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Schimke immuno-osseous dysplasia. A pediatric disease reaches adulthood].
  • [Transliterated title] Schimke-immunoossäre Dysplasie. Eine pädiatrische Erkrankung wird erwachsen.
  • BACKGROUND: Schimke immuno-osseous dysplasia (SIOD) is a rare autosomal recessive multisystemic disorder caused by mutations of the SMARCAL 1 gene (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a-like 1).
  • CLINICAL FEATURES: Main clinical features are: disproportional growth deficiency due to spondyloepiphyseal dysplasia, nephrotic syndrome with focal and segmental glomerulosclerosis, and defective cellular immunity.

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  • (PMID = 16648978.001).
  • [ISSN] 0723-5003
  • [Journal-full-title] Medizinische Klinik (Munich, Germany : 1983)
  • [ISO-abbreviation] Med. Klin. (Munich)
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] EC 2.7.7.- / SMARCAL1 protein, human; EC 3.6.4.- / DNA Helicases
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35. Kaftan H, Adamaszek M, Hosemann W: [Mondini dysplasia: traumatic cerebrospinal fluid otorrhea with meningitis]. HNO; 2006 Aug;54(8):624-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Mondini dysplasia: traumatic cerebrospinal fluid otorrhea with meningitis].
  • [Transliterated title] Mondini-Dysplasie: Traumatische Otoliquorrhö mit Meningoenzephalitis.
  • Mondini dysplasia is a rare malformation of the inner ear commonly associated with loss of hearing and vestibular function.
  • Children with Mondini dysplasia are predisposed to developing a spontaneous cerebrospinal fluid (CSF) leak and recurrent meningitis.
  • We describe a 65-year-old man with unrecognized unilateral Mondini dysplasia who presented with CSF leak and meningoencephalitis after minor head trauma.
  • Patients with Mondini dysplasia or their parents should be cautioned about the potential hazards of any head trauma.

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  • (PMID = 16205869.001).
  • [ISSN] 0017-6192
  • [Journal-full-title] HNO
  • [ISO-abbreviation] HNO
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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36. Sengers FB, van Lijnschoten G, van der Sluijs-Bens JP, Porath MM, Dijkman KP: [Haematological abnormalities in premature babies due to placental mesenchymal dysplasia]. Ned Tijdschr Geneeskd; 2010;154:A1040

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Haematological abnormalities in premature babies due to placental mesenchymal dysplasia].
  • [Transliterated title] Hematologische afwijkingen bij prematuur pasgeborenen door placentaire mesenchymale dysplasie.
  • The first patient also had intra-uterine growth restriction.
  • A postpartum pathological examination showed abnormalities of both placentae consistent with placental mesenchymal dysplasia.
  • Placental mesenchymal dysplasia is a rare condition which is associated with intra-uterine growth restriction, intra-uterine mortality, prematurity and Beckwith-Wiedemann syndrome.
  • Both children had unrestricted growth and development patterns at one year and 6 months follow-up, respectively.
  • [MeSH-minor] Diagnosis, Differential. Female. Fetal Growth Retardation / pathology. Fetal Growth Retardation / ultrasonography. Humans. Infant, Newborn. Infant, Premature. Pregnancy. Pregnancy Outcome

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  • (PMID = 20356428.001).
  • [ISSN] 1876-8784
  • [Journal-full-title] Nederlands tijdschrift voor geneeskunde
  • [ISO-abbreviation] Ned Tijdschr Geneeskd
  • [Language] dut
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Netherlands
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37. Kramer BW, Lievense S, Been JV, Zimmermann LJ: [From classic to new bronchopulmonary dysplasia]. Ned Tijdschr Geneeskd; 2010;154:A1024
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [From classic to new bronchopulmonary dysplasia].
  • [Transliterated title] Van klassieke naar nieuwe bronchopulmonale dysplasie.
  • Chronic lung damage (bronchopulmonary dysplasia (BPD)) is one of the most serious complications affecting preterm neonates.
  • [MeSH-major] Anti-Inflammatory Agents / therapeutic use. Bronchopulmonary Dysplasia / drug therapy. Bronchopulmonary Dysplasia / etiology. Pulmonary Surfactants / therapeutic use. Respiration, Artificial / adverse effects

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  • (PMID = 20456770.001).
  • [ISSN] 1876-8784
  • [Journal-full-title] Nederlands tijdschrift voor geneeskunde
  • [ISO-abbreviation] Ned Tijdschr Geneeskd
  • [Language] dut
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Netherlands
  • [Chemical-registry-number] 0 / Anti-Inflammatory Agents; 0 / Pulmonary Surfactants; S88TT14065 / Oxygen
  • [Number-of-references] 25
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38. Groneck P, Speer CP: [Pharmacological prophylaxis and treatment of bronchopulmonary dysplasia]. Z Geburtshilfe Neonatol; 2005 Aug;209(4):119-27
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Pharmacological prophylaxis and treatment of bronchopulmonary dysplasia].
  • [Transliterated title] Medikamentöse Prophylaxe und Therapie der bronchopulmonalen Dysplasie.
  • Treatment with prenatal steroids, prophylactic or early therapeutic surfactant substitution, application of early nasal CPAP, minimizing of mechanical ventilation, early treatment of PDA and avoiding nosocomial infections are the main measures to prevent the development of bronchopulmonary dysplasia (BPD) in high-risk pre-term neonates.
  • [MeSH-major] Adrenal Cortex Hormones / administration & dosage. Bronchodilator Agents / administration & dosage. Bronchopulmonary Dysplasia / prevention & control. Diuretics / administration & dosage. Vaccination. Vasodilator Agents / administration & dosage. Vitamin A / administration & dosage

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  • (PMID = 16138269.001).
  • [ISSN] 0948-2393
  • [Journal-full-title] Zeitschrift für Geburtshilfe und Neonatologie
  • [ISO-abbreviation] Z Geburtshilfe Neonatol
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Adrenal Cortex Hormones; 0 / Bronchodilator Agents; 0 / Diuretics; 0 / Vasodilator Agents; 11103-57-4 / Vitamin A
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39. Hatt Brupbacher SC, Job O, Senn P, Dedes W: [Ophthalmological findings in microcephaly-lymphoedema-chorioretinal dysplasia syndrome]. Klin Monbl Augenheilkd; 2009 Apr;226(4):344-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Ophthalmological findings in microcephaly-lymphoedema-chorioretinal dysplasia syndrome].
  • [Transliterated title] Okuläre Veränderungen beim Mikrozephalie-Lymphödem-Chorioretinale-Dysplasie-Syndrom.
  • BACKGROUND: Microcephaly-lymphoedema-chorioretinal dysplasia (MLCRD) is a rare syndrome characterized by microcephaly, chorioretinal dysplasia, lymphoedema and a characteristic facial phenotype.
  • HISTORY AND SIGNS: A three-month-old boy with intrauterine growth retardation and microcephaly was referred to our clinic.
  • On funduscopy of the right eye pale optic disc, chorioretinal dysplasia with pigmentary and atrophic changes and falciform folds were noted.
  • Parents and grandparents should also be considered for eye examination if a child has chorioretinal dysplasia and microcephaly.
  • [MeSH-major] Abnormalities, Multiple / diagnosis. Abnormalities, Multiple / genetics. Choroid / abnormalities. Lymphedema / diagnosis. Lymphedema / genetics. Microcephaly / diagnosis. Microcephaly / genetics. Retinal Dysplasia / diagnosis. Retinal Dysplasia / genetics

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  • (PMID = 19384796.001).
  • [ISSN] 1439-3999
  • [Journal-full-title] Klinische Monatsblätter für Augenheilkunde
  • [ISO-abbreviation] Klin Monbl Augenheilkd
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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40. Garweg C, Mélon P, Waleffe A, Piérard L: [Arrhythmogenic right ventricular dysplasia]. Rev Med Liege; 2006 Sep;61(9):632-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Arrhythmogenic right ventricular dysplasia].
  • [Transliterated title] Dysplasie arythmogène du ventricule droit.
  • Arrhythmogenic right ventricular dysplasia is an unfrequent disease that associates ventricular tachycardia with left bundle branch block morphology and right ventricular fibro-fatty degeneration.
  • [MeSH-major] Arrhythmogenic Right Ventricular Dysplasia

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  • (PMID = 17112163.001).
  • [ISSN] 0370-629X
  • [Journal-full-title] Revue médicale de Liège
  • [ISO-abbreviation] Rev Med Liege
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Belgium
  • [Number-of-references] 18
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41. Karila C, Saulnier JP, Elie C, Taupin P, Scheinmann P, Le Bourgeois M, Waernessycle S, de Blic J: [Exercise alveolar hypoventilation in long-term survivors of bronchopulmonary dysplasia]. Rev Mal Respir; 2008 Mar;25(3):303-12
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Exercise alveolar hypoventilation in long-term survivors of bronchopulmonary dysplasia].
  • [Transliterated title] Hypoventilation alvéolaire à l'exercice chez des enfants avec dysplasie bronchopulmonaire.
  • BACKGROUND: We aimed to confirm that children who have survived bronchopulmonary dysplasia (BPD) display lower ventilation during exercise than healthy children, and to determine whether alveolar hypoventilation associated with exercise-induced hypoxemia occurred in these children.
  • [MeSH-major] Bronchopulmonary Dysplasia / complications. Exercise Test. Hypoventilation / etiology

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  • [CommentIn] Rev Mal Respir. 2008 Mar;25(3):271-2 [18449092.001]
  • (PMID = 18449096.001).
  • [ISSN] 0761-8425
  • [Journal-full-title] Revue des maladies respiratoires
  • [ISO-abbreviation] Rev Mal Respir
  • [Language] fre
  • [Publication-type] Controlled Clinical Trial; English Abstract; Journal Article
  • [Publication-country] France
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42. Egner-Höbarth S, Welkerling H, Windhager R: [Bisphosphonates in the therapy of fibrous dysplasia. Relevant data and practical aspects]. Orthopade; 2007 Feb;36(2):124, 126-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Bisphosphonates in the therapy of fibrous dysplasia. Relevant data and practical aspects].
  • [Transliterated title] Bisphosphonate in der Therapie der fibrösen Dysplasie. Relevante Daten und praktische Aspekte.
  • Fibrous dysplasia covers a variety of rather different clinical pictures.
  • The literature as well as personal experience show them to be an especially valid option for the treatment of polyostotic fibrous dysplasia and the various syndromes.
  • [MeSH-major] Bone Density Conservation Agents / therapeutic use. Diphosphonates / therapeutic use. Fibrous Dysplasia of Bone / drug therapy

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  • (PMID = 17277960.001).
  • [ISSN] 0085-4530
  • [Journal-full-title] Der Orthopäde
  • [ISO-abbreviation] Orthopade
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Bone Density Conservation Agents; 0 / Diphosphonates
  • [Number-of-references] 28
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43. Heuberger BM, Bornstein MM, Reichart PA, Hürlimann S, Kuttenberger JJ: [Periapical osseous dysplasia of the anterior maxilla--a case presentation]. Schweiz Monatsschr Zahnmed; 2010;120(11):1001-11

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Periapical osseous dysplasia of the anterior maxilla--a case presentation].
  • [Transliterated title] Periapikale ossäre Dysplasie der anterioren Maxilla. Ein Fallbericht.
  • Osseous dysplasias (formerly cemento-osseous dysplasias/ CODs) represent a specific clinico-pathologic spectrum of related, non-neoplastic benign fibro-osseous lesions.
  • Osseous dysplasias are often identified as an incidental finding on standard dental radiographs of adults.
  • Four different types of ODs can be distinguished: the periapical osseous dysplasia (POD), the focal osseous dysplasia (FocOD), the florid osseous dysplasia (FOD) and the familial gigantiform cementoma.
  • This case report presents an unusual localization of a periapical osseous dysplasia (POD) in the anterior maxillary bone in a 33-year old female patient of Caucasian origin.

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  • (PMID = 21545031.001).
  • [ISSN] 0256-2855
  • [Journal-full-title] Schweizer Monatsschrift fur Zahnmedizin = Revue mensuelle suisse d'odonto-stomatologie = Rivista mensile svizzera di odontologia e stomatologia
  • [ISO-abbreviation] Schweiz Monatsschr Zahnmed
  • [Language] FRE; GER
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Switzerland
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44. Vrijlandt EJ, Gerritsen J, Duiverman EJ: [Bronchopulmonary dysplasia in ex-prematures approaching adulthood]. Ned Tijdschr Geneeskd; 2007 Nov 3;151(44):2445-51
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Bronchopulmonary dysplasia in ex-prematures approaching adulthood].
  • [Transliterated title] Bronchopulmonale dysplasie bij ex-prematuren die volwassen worden.
  • Many patients born prematurely who developed bronchopulmonary dysplasia (BPD) as neonates are now approaching adulthood.
  • [MeSH-major] Bronchopulmonary Dysplasia / physiopathology. Infant, Premature

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  • (PMID = 18064864.001).
  • [ISSN] 0028-2162
  • [Journal-full-title] Nederlands tijdschrift voor geneeskunde
  • [ISO-abbreviation] Ned Tijdschr Geneeskd
  • [Language] dut
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Netherlands
  • [Number-of-references] 27
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45. Baretton GB, Aust DE: [Intraepithelial neoplasia/dysplasia - histopathology in ulcerative colitis]. Pathologe; 2008 Nov;29 Suppl 2:280-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Intraepithelial neoplasia/dysplasia - histopathology in ulcerative colitis].
  • [Transliterated title] Intraepitheliale Neoplasie/Dysplasie - Diagnose bei Colitis ulcerosa.
  • Intraepithelial neoplasia/dysplasia in the setting of IBD is considered a precancerous lesion by definition.
  • Intraepithelial neoplasia may present itself either as a flat or polypoid mucosal lesion and is referred to as a dysplasia-associated lesion or mass (DALM) in the latter case.
  • The therapeutic consequence of high-grade intraepithelial neoplasia/dysplasia and/or DALM is proctocolectomy in most centers because of the high risk of synchronous or metachronous CRC.

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  • (PMID = 18820923.001).
  • [ISSN] 1432-1963
  • [Journal-full-title] Der Pathologe
  • [ISO-abbreviation] Pathologe
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
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46. Madersbacher S, Ponholzer A, Franz K, Höltl W: [Synchronous bilateral renal cell cancer with a single ovarian metastasis and a fibromuscular dysplasia of the renal artery]. Aktuelle Urol; 2007 Jan;38(1):52-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Synchronous bilateral renal cell cancer with a single ovarian metastasis and a fibromuscular dysplasia of the renal artery].
  • [Transliterated title] Synchroner bilateraler Nierentumor mit singulärer Ovarialmetastase und fibromuskulärer Dysplasie der Nierenarterie.
  • Prior to nephron-sparing surgery of the left kidney an angiography was performed revealing a massive fibromuscular dysplasia.
  • The presented case was unique because of synchronous bilateral RCC, an ovarian metastasis and a fibromuscular dysplasia of the renal artery requiring a sophisticated surgical approach.
  • [MeSH-major] Carcinoma, Renal Cell / secondary. Fibromuscular Dysplasia / diagnosis. Kidney Neoplasms / diagnosis. Neoplasms, Multiple Primary / secondary. Ovarian Neoplasms / secondary. Renal Artery Obstruction / diagnosis


47. Papageorgiou E, Schiefer U, Warmuth-Metz M, Weckerle P: [Morning glory disc anomaly und frontonasal dysplasia]. Ophthalmologe; 2007 Aug;104(8):709-12
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Morning glory disc anomaly und frontonasal dysplasia].
  • [Transliterated title] Morning-glory-Papille und frontonasale Dysplasie.


48. Scoazec JY: [Dysplasia in glandular digestive tissues: new concepts, new classifications]. Ann Pathol; 2007 Dec;27(6):398-416

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Dysplasia in glandular digestive tissues: new concepts, new classifications].
  • [Transliterated title] Dysplasie en muqueuses glandulaires digestives: nouvelles terminologies, nouvelles classifications.
  • The term of dysplasia is currently used to designate morphological alterations, identifiable at microscopic examination, revealing the existence of an unequivocally neoplastic process, at an early, non-invasive, stage of its natural history.
  • The pathologist bears the full responsibility for the diagnosis of dysplasia, based on a broad spectrum of cytological and architectural abnormalities.
  • It is important to grade the severity of the dysplastic lesions, in order to help guide clinical management and choose the therapeutic strategy.
  • The Vienna classification, proposed in 2000 as a compromise between the Western and Japanese concepts, is now used for classification and grading of digestive epithelial dysplasia.

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  • (PMID = 18554550.001).
  • [ISSN] 0242-6498
  • [Journal-full-title] Annales de pathologie
  • [ISO-abbreviation] Ann Pathol
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
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49. Khelifi S, Bouhafa A, Agrebi W, Cherif A, Ben M, Khayat O, Letaief A: [Filiation hamartoma polyposis dysplasia and small bowel adenocarcinoma]. Tunis Med; 2006 Feb;84(2):128-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Filiation hamartoma polyposis dysplasia and small bowel adenocarcinoma].
  • [Transliterated title] La filiation polype hamartmateux-dysplasie-adenocarcinome.
  • Dysplasia is rare.
  • Transformation of the polyposis hamartoma into a site of dysplasia then into adenocarcinoma has been rarely reported.
  • The authors report the case of a 14 year-old patient, having a severe dysplasia on ileal polyposis hamartoma related to the syndrome of Peutz-Jeghers.

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  • (PMID = 16755980.001).
  • [ISSN] 0041-4131
  • [Journal-full-title] La Tunisie médicale
  • [ISO-abbreviation] Tunis Med
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Tunisia
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50. Orcel P, Chapurlat R: [Fibrous dysplasia of bone]. Rev Prat; 2007 Oct 31;57(16):1749-55
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Fibrous dysplasia of bone].
  • [Transliterated title] Dysplasie fibreuse des os.
  • Fibrous dysplasia of bone is a congenital non hereditary benign bone disease, where normal bone is replaced by a fibrous-like tissue with immature osteogenesis.
  • [MeSH-major] Fibrous Dysplasia of Bone / congenital

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  • (PMID = 18092715.001).
  • [ISSN] 0035-2640
  • [Journal-full-title] La Revue du praticien
  • [ISO-abbreviation] Rev Prat
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Bone Density Conservation Agents; 0 / Diphosphonates; 0 / Phosphates; EC 3.6.1.- / GNAS protein, human; EC 3.6.5.1 / GTP-Binding Protein alpha Subunits, Gs; FXC9231JVH / Calcitriol
  • [Number-of-references] 21
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51. Frank R, Al Daoud Zenner M, Tonet J, Lucet FH, Himbert C, Hulot JS, Lacotte G, Fontaine G: [Arrhythmogenic right ventricular dysplasia and sudden cardiac death]. Ann Cardiol Angeiol (Paris); 2005 Jan;54(1):21-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Arrhythmogenic right ventricular dysplasia and sudden cardiac death].
  • [Transliterated title] Dysplasie ventriculaire droite arythmogène et mort subite.
  • [MeSH-major] Arrhythmogenic Right Ventricular Dysplasia / complications. Death, Sudden, Cardiac / etiology

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  • (PMID = 15702907.001).
  • [ISSN] 0003-3928
  • [Journal-full-title] Annales de cardiologie et d'angéiologie
  • [ISO-abbreviation] Ann Cardiol Angeiol (Paris)
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Anti-Arrhythmia Agents
  • [Number-of-references] 20
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52. Ezzine Sebai N, Khaled A, Kharfi M, Bouzgarrou A, M'halla H, Jones M, Fazaa B, Kamoun MR: [Anhidrotic/hypohidrotic ectodermal dysplasia: ten cases]. Tunis Med; 2009 Dec;87(12):805-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Anhidrotic/hypohidrotic ectodermal dysplasia: ten cases].
  • [Transliterated title] Dysplasie ectodermique hypo/anhidrotique: 10 observations.
  • BACKGROUND: Ectodermal dysplasias are rare hereditary diseases characterised by congenital absence of ectodermally derived structures and classified according to four symptoms: trichodysplasia, hypodontia, onychodysplasia and hypohidrosis.
  • AIM: The objective of our study is to precise the epidemioclinical characteristics, the diagnostic tools, the evolution and the treatments of this rare disease through a 10-case series of hypohidrotic ectodermal dysplasia (HED).
  • METHODS: The present report is a retrospective study of all cases of an/hypohidrotic ectodermal dysplasia collected from 1977 to 2006.
  • [MeSH-major] Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive / diagnosis


53. Blum A: [Severely dysplastic nevus: atypical Spitz nevus or melanoma in situ?]. Hautarzt; 2010 Feb;61(2):151-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Severely dysplastic nevus: atypical Spitz nevus or melanoma in situ?].
  • [Transliterated title] Nävus mit schwerer Dysplasie, atypischer Nävus Spitz oder Melanoma in situ?
  • Histological analysis showed it to be a severely dysplastic melanocytic nevus.
  • [MeSH-major] Dysplastic Nevus Syndrome / pathology. Melanoma / pathology. Nevus, Epithelioid and Spindle Cell / pathology. Skin Neoplasms / pathology

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  • (PMID = 20135253.001).
  • [ISSN] 1432-1173
  • [Journal-full-title] Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete
  • [ISO-abbreviation] Hautarzt
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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54. Ziadi S, Trimeche M, Mokni M, Sriha B, Khochtali H, Korbi S: [Eighteen cases of craniofacial fibrous dysplasia]. Rev Stomatol Chir Maxillofac; 2009 Dec;110(6):318-22
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Eighteen cases of craniofacial fibrous dysplasia].
  • [Transliterated title] Dix-huit cas de dysplasie fibreuse craniofaciale.
  • INTRODUCTION: Fibrous dysplasia or Jaffe Lischtenstein's disease is sporadic and rare bone affection, mainly observed in young adults.
  • Fibrous dysplasia is relatively rare in the craniofacial region, (only 20% of all locations).
  • The authors analyzed the epidemiological, anatomoclinical and evolutive features of fibrous dysplasia in a Tunisian population.
  • MATERIAL AND METHOD: The authors retrospectively studied 18 cases of craniofacial fibrous dysplasia, diagnosed at the pathology department of the Sousse F.
  • RESULTS: Most craniofacial dysplasia cases were monostotic (94% of cases).
  • [MeSH-major] Facial Bones / pathology. Fibrous Dysplasia, Monostotic / epidemiology

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  • (PMID = 19615708.001).
  • [ISSN] 1776-257X
  • [Journal-full-title] Revue de stomatologie et de chirurgie maxillo-faciale
  • [ISO-abbreviation] Rev Stomatol Chir Maxillofac
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
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55. Verstrynge A, Carels C, Verdonck A, Mollemans W, Willems G, Schoenaers J: [Dentomaxillary and -facial problems in cleidocranial dysplasia]. Ned Tijdschr Tandheelkd; 2006 Feb;113(2):69-74
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Dentomaxillary and -facial problems in cleidocranial dysplasia].
  • [Transliterated title] Dentomaxillaire en -faciale problemen bij cleidocraniale dysplasie.
  • A 14-year old boy with cleidocranial dysplasia was referred because of an almost complete presence of the deciduous dentition.
  • [MeSH-major] Cleidocranial Dysplasia / complications. Tooth, Supernumerary / surgery

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  • (PMID = 16509515.001).
  • [ISSN] 0028-2200
  • [Journal-full-title] Nederlands tijdschrift voor tandheelkunde
  • [ISO-abbreviation] Ned Tijdschr Tandheelkd
  • [Language] dut
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Netherlands
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56. Soubeyrand E, Nicolas J, Labbé D, Riscala S, Olive L, Compère JF, Bénateau H: [Anhidrotic ectomermal dysplasia (AED): four cases]. Rev Stomatol Chir Maxillofac; 2005 Dec;106(6):328-33

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Anhidrotic ectomermal dysplasia (AED): four cases].
  • [Transliterated title] La dysplasie ectodermique anhydrotique: présentation de quatre observations.
  • INTRODUCTION: Anhidrotic ectodermal dysplasia (AED) or Christ-Siemens-Touraine syndrome is a rare, hereditary genodermatosis, classically X-linked recessive disorder.
  • Once the diagnosis is established, family investigations are necessary to determine whether it is a family form or a new sporadic case.
  • Symptomatic maxillo-facial treatment strives to improve masticatory function and facial growth and thus limit the psychological impact and improve patient comfort.
  • [MeSH-major] Ectodermal Dysplasia / complications

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  • (PMID = 16344753.001).
  • [ISSN] 0035-1768
  • [Journal-full-title] Revue de stomatologie et de chirurgie maxillo-faciale
  • [ISO-abbreviation] Rev Stomatol Chir Maxillofac
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
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57. Allias F, Lebreton F, Collardeau-Frachon S, Vasiljevic A, Rossignol S, Massardier J, Huissoud C, Devouassoux-Shisheboran M: [Placental mesenchymal dysplasia]. Ann Pathol; 2008 Apr;28(2):85-94
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Placental mesenchymal dysplasia].
  • [Transliterated title] La dysplasie mésenchymateuse du placenta.
  • Placental mesenchymal dysplasia (PMD) is a recently described entity.
  • However, careful microscopic examination, cytogenetic analyses, molecular studies and follow-up of children allowed to better understand this placental abnormality, allowing an antenatal diagnosis.

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  • (PMID = 18675158.001).
  • [ISSN] 0242-6498
  • [Journal-full-title] Annales de pathologie
  • [ISO-abbreviation] Ann Pathol
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
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58. Vignon-Savoye C, Le Merrer M, Vincens A, Monfort M, Talon P: [Ghosal haematodiaphyseal dysplasia: a new case]. Arch Pediatr; 2005 Aug;12(8):1244-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Ghosal haematodiaphyseal dysplasia: a new case].
  • [Transliterated title] Un nouveau cas de dysplasie hématodiaphysaire de Ghosal.
  • Ghosal-type hematodiaphyseal dysplasia has been first described in 1986, as a steroid-dependent anemia with endosteal broadening of the long bone's diaphyses and metaphaphyses, which makes a distinction with the periosteal reaction in Camuratti-Engelmann's disease and with Caffey's disease.

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  • (PMID = 16051078.001).
  • [ISSN] 0929-693X
  • [Journal-full-title] Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie
  • [ISO-abbreviation] Arch Pediatr
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Adrenal Cortex Hormones
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59. Napp M, Stengel BA, Buschmann J, Döhler JR: [Osteofibrous dysplasia campanacci of the tibia. A 12-year follow-up]. Chirurg; 2009 Mar;80(3):241-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Osteofibrous dysplasia campanacci of the tibia. A 12-year follow-up].
  • [Transliterated title] Osteofibröse Dysplasie Campanacci der Tibia : Ein 12-Jahres-Follow-up.
  • Pathologic fractures and deformities are common complications of osteofibrous dysplasia.
  • [MeSH-major] Fibrous Dysplasia of Bone / surgery. Fractures, Spontaneous / surgery. Tibial Fractures / surgery

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  • (PMID = 18690418.001).
  • [ISSN] 1433-0385
  • [Journal-full-title] Der Chirurg; Zeitschrift für alle Gebiete der operativen Medizen
  • [ISO-abbreviation] Chirurg
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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60. Darbi A, Cenoui F, Atmane A, Amil T, Hanine A: [Cochleovestibular dysplasia: a case report]. Arch Pediatr; 2010 Apr;17(4):378-82
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Cochleovestibular dysplasia: a case report].
  • [Transliterated title] Dysplasie cochléovestibulaire. A propos d'un cas.
  • Cochleovestibular dysplasia or Mondini malformation is exceptional.
  • Cochlear dysplasia is due to early cessation of the development of the inner ear during embryonic life.

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  • [Copyright] Copyright 2010 Elsevier Masson SAS. All rights reserved.
  • (PMID = 20189363.001).
  • [ISSN] 1769-664X
  • [Journal-full-title] Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie
  • [ISO-abbreviation] Arch Pediatr
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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61. Arkha Y, Benazzou S, Harmouch A, Derraz S, El Ouahabi A, El Khamlichi A: [A case of cystic craniofacial fibrous dysplasia]. Rev Stomatol Chir Maxillofac; 2010 Apr;111(2):101-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [A case of cystic craniofacial fibrous dysplasia].
  • [Transliterated title] Un cas de dysplasie fibreuse kystique craniofaciale.
  • INTRODUCTION: Fibrous dysplasia is a benign, idiopathic, fibro-osseous disease.
  • The radiological appearance suggested a mucocele but histological examination, after surgery, proved a fibrous dysplasia.
  • DISCUSSION: Fibrous dysplasia with fronto-sphenoido-ethmoidal localization may be misdiagnosed as mucocele.
  • [MeSH-major] Bone Cysts / surgery. Fibrous Dysplasia, Polyostotic / surgery. Skull / surgery

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  • [CommentIn] Rev Stomatol Chir Maxillofac. 2010 Sep;111(4):244-6 [20656311.001]
  • (PMID = 20359731.001).
  • [ISSN] 1776-257X
  • [Journal-full-title] Revue de stomatologie et de chirurgie maxillo-faciale
  • [ISO-abbreviation] Rev Stomatol Chir Maxillofac
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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62. Chêne G, Penault-Llorca F, Le Bouëdec G, Mishellany F, Dauplat MM, Tardieu AS, Pomel C, Jaffeux P, Aublet-Cuvelier B, Pouly JL, Déchelotte P, Dauplat J: [Ovarian epithelial dysplasia: myth or reality? Review]. Gynecol Obstet Fertil; 2008 Jul-Aug;36(7-8):800-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Ovarian epithelial dysplasia: myth or reality? Review].
  • [Transliterated title] Dysplasie épithéliale ovarienne: mythe ou réalité? Revue de la littérature.
  • Ovarian epithelial dysplasia has been described in the ovarian surface epithelium by histologic, morphometric and nuclear profile studies.
  • Diagnosis and identification of ovarian dysplasia would certainly be useful to understand the early steps of ovarian carcinogenesis.
  • However, dysplasia in relation with ovulation induction seems to have a different pattern.
  • We report dysplasia definitions and the current clinical management.
  • [MeSH-major] Ovarian Diseases / pathology. Uterine Cervical Dysplasia / pathology

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  • (PMID = 18657463.001).
  • [ISSN] 1297-9589
  • [Journal-full-title] Gynécologie, obstétrique & fertilité
  • [ISO-abbreviation] Gynecol Obstet Fertil
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Number-of-references] 64
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63. Tomb R, Soutou B, Zalloua P: [Anhidrotic ectodermal dysplasia. Report of a rare mutation in EDA1]. Ann Dermatol Venereol; 2009 Jan;136(1):28-31
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Anhidrotic ectodermal dysplasia. Report of a rare mutation in EDA1].
  • [Transliterated title] Dysplasie ectodermique anhidrotique familiale: une mutation rare du gène EDA1.
  • BACKGROUND: Anhidrotic ectodermal dysplasia is a rare inherited disorder seen mainly in the X-linked recessive form.
  • DISCUSSION: Ectodermal dysplasias are currently found in more than 150 syndromes.
  • The patient's history and the clinical signs suggest the X-linked recessive form of anhidrotic ectodermal dysplasia due to a mutation in EDA1 gene encoding the ectodysplasin.
  • [MeSH-major] Ectodermal Dysplasia / genetics. Ectodysplasins / genetics. Mutation, Missense

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  • (PMID = 19171226.001).
  • [ISSN] 0151-9638
  • [Journal-full-title] Annales de dermatologie et de vénéréologie
  • [ISO-abbreviation] Ann Dermatol Venereol
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Codon; 0 / Dermatologic Agents; 0 / EDA protein, human; 0 / Ectodysplasins; EH28UP18IF / Isotretinoin
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64. Langlais F, Frieh JM, Gédouin JE, Gouin F, Hulet C, Abadie P, Lambotte JC, Lannou R, Marin F, Richter D, Sadri H, Than Trong V, Vielpeau C: [Hip dysplasia and misalignment in patients aged 20-50 years]. Rev Chir Orthop Reparatrice Appar Mot; 2006 Jun;92(4 Suppl):1S41-1S81
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Hip dysplasia and misalignment in patients aged 20-50 years].
  • [Transliterated title] Dysplasie et conflits de hanche de 20 à 50 ans.
  • Anterior hip pain in young adult (20 to 50) has two main causes: secondary osteo-arthritis on development dysplasia of the hip, and femoro-acetabular impigement (FAI).
  • The second part concerned the different syndromes with acute anterior hip pain, especially due to FAI and to labral tears.In hip dysplasia, 56 shelf operations, 100 proximal femoral varus osteotomies associated or not with a shelf arthroplasty,and 127 Chiari osteotomies were examined with 10 years minimum follow-up.
  • The 3 main factors of good prognosis were: a complete correction of both femoral and acetabular dysplasia; age at operation under 40; a moderate arthritis (grade I or II according to De Mourgues and Patte).
  • In single acetabular dysplasia with 3 favorable prognosis factors(no coxa valga, age under 40, arthritis 1 or 2), 85% good results were achieved at 15 years.
  • Therefore, with 85% good results at 15 years (and often over 20 years), non prosthetic surgery performed at 30-35 years, achieved better functional results than total hip arthroplasty, longer lasting, and not jeopardizing any further possibility of prosthetic surgery.As concerns acute anterior pain of the hip, the clinical and imaging patterns of the different syndromes have been precised: femoro-acetabular impigement by cam (or by pincer), labral tears in hip dysplasia.

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  • (PMID = 16767027.001).
  • [ISSN] 1776-2553
  • [Journal-full-title] Revue de chirurgie orthopédique et réparatrice de l'appareil moteur
  • [ISO-abbreviation] Rev Chir Orthop Reparatrice Appar Mot
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
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65. Flecher X, Argenson JN, Parratte S, Ryembault E, Aubaniac JM: [Custom cementless stem for osteoarthritis following developmental hip dysplasia]. Rev Chir Orthop Reparatrice Appar Mot; 2006 Jun;92(4):332-42
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Custom cementless stem for osteoarthritis following developmental hip dysplasia].
  • [Transliterated title] Tiges fémorales sur mesure non cimentées pour séquelle de dysplasie et luxation congénitale de hanche.
  • PURPOSE OF THE STUDY: Arthroplasty in developmental dysplasia of the hip joint raises technical problems related to the anatomy and age of the young patient.
  • RESULTS: The series included 174 cases of dysplasia and 83 dislocations, 39% stage 1, 30% stage 2, 14% stage 3 and 17% stage 4.
  • DISCUSSION: This study confirmed the anatomic modifications observed in patients with developmental hip dysplasia and the surgical problems they cause.

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  • (PMID = 16948460.001).
  • [ISSN] 0035-1040
  • [Journal-full-title] Revue de chirurgie orthopédique et réparatrice de l'appareil moteur
  • [ISO-abbreviation] Rev Chir Orthop Reparatrice Appar Mot
  • [Language] fre
  • [Publication-type] Comparative Study; English Abstract; Journal Article
  • [Publication-country] France
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66. Harou K, L'Hermite M: [Asphyxiating thoracic dysplasia (Jeune syndrome): about two cases]. J Gynecol Obstet Biol Reprod (Paris); 2010 Apr;39(2):163-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Asphyxiating thoracic dysplasia (Jeune syndrome): about two cases].
  • [Transliterated title] Dysplasie thoracique asphyxiante ou syndrome de Jeune: à propos de deux cas.
  • Asphyxiating thoracic dysplasia (Jeune syndrome) is an osteochondrodysplasia with autosomal recessive inheritance, characterised by a nanism with rhizomelic predominance, associated with a narrow thorax.

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  • [Copyright] (c) 2009 Elsevier Masson SAS. All rights reserved.
  • (PMID = 19853385.001).
  • [ISSN] 1773-0430
  • [Journal-full-title] Journal de gynécologie, obstétrique et biologie de la reproduction
  • [ISO-abbreviation] J Gynecol Obstet Biol Reprod (Paris)
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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67. Bruder E, Meier-Ruge WA: [Intestinal neuronal dysplasia type B: how do we understand it today?]. Pathologe; 2007 Mar;28(2):137-42
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Intestinal neuronal dysplasia type B: how do we understand it today?].
  • [Transliterated title] Intestinale neuronale Dysplasie Typ B: Wie verstehen wir sie heute?
  • Intestinal neuronal dysplasia type B (IND B) is currently considered to be a subtle malformation of the submucosal plexus, leading to an increased proportion of over-sized ganglia and potentially accompanied by a mild, chronic gastrointestinal motility disturbance.

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  • (PMID = 17279410.001).
  • [ISSN] 0172-8113
  • [Journal-full-title] Der Pathologe
  • [ISO-abbreviation] Pathologe
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
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68. Gagnon RF, Kintzen G, Thérasse E: [Endovascular treatment of a renal artery aneurysm and stenosis due to fibromuscular dysplasia]. Nephrol Ther; 2008 Oct;4(5):347-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Endovascular treatment of a renal artery aneurysm and stenosis due to fibromuscular dysplasia].
  • [Transliterated title] Traitement endovasculaire d'un anévrisme et d'une sténose de l'artère rénale secondaires à une dysplasie fibromusculaire.


69. Van Linthoudt D: [Patellar hypertrophy: rare abnormality associated with a multiple epiphyseal dysplasia]. Praxis (Bern 1994); 2008 Aug 13;97(16):893-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Patellar hypertrophy: rare abnormality associated with a multiple epiphyseal dysplasia].
  • [Transliterated title] Hypertrophie rotulienne: rare anomalie associée a une dysplasie polyépiphysaire.
  • Multiple epiphyseal dysplasia is a genotypic chondrodystrophy characterized by an abnormal shape of numerous epiphyses.
  • Diagnosis is usually made during childhood on an abnormal gait and a reduction of joint mobility associated with radiological changes of the ossification centres.
  • Persistence of both ossification centres could result in a coronal double-layered patella, which is also occasionally observed in patients with multiple epiphyseal dysplasia.

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  • (PMID = 18777717.001).
  • [ISSN] 1661-8157
  • [Journal-full-title] Praxis
  • [ISO-abbreviation] Praxis (Bern 1994)
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Switzerland
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70. Schipper J, Maier W, Berlis A, Ridder GJ: [Computer-assisted surgery (CAS) for the optimal treatment of craniofacial fibrous dysplasia]. HNO; 2005 Sep;53(9):766-72
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Computer-assisted surgery (CAS) for the optimal treatment of craniofacial fibrous dysplasia].
  • [Transliterated title] Computerassistierte Chirurgie (CAS) zur optimalen Behandlung der kraniofazialen fibrösen Dysplasie.
  • BACKGROUND AND OBJECTIVE: The rare bone disease craniofacial fibrous dysplasia is only treated in cases of visible deformities of the splanchnocranium and neurocranium, compression syndromes, and delocation of nasal and paranasal drainage.
  • METHODS AND PATIENTS: In a retrospective quality assessment analysis of six patients with craniofacial monostotic fibrous dysplasia, the indications were analysed for situations in which computer-assisted surgery (CAS) might be helpful.
  • [MeSH-major] Facial Bones / surgery. Fibrous Dysplasia, Polyostotic / surgery. Preoperative Care / methods. Radiographic Image Interpretation, Computer-Assisted / methods. Reconstructive Surgical Procedures / methods. Skull / surgery. Surgery, Computer-Assisted / methods

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  • (PMID = 15551019.001).
  • [ISSN] 0017-6192
  • [Journal-full-title] HNO
  • [ISO-abbreviation] HNO
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
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71. Ayadi-Kaddour A, Ben Slama S, Marghli A, Mehouachi R, Djilani H, Kilani T, El Mezni F: [Fibrous dysplasia of the rib. Ten case reports]. Rev Chir Orthop Reparatrice Appar Mot; 2008 May;94(3):301-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Fibrous dysplasia of the rib. Ten case reports].
  • [Transliterated title] Dysplasie fibreuse costale. A propos de dix cas.
  • We report a series of 10 cases of costal fibrous dysplasia.
  • Plain X-rays showed signs suggestive of fibrous dysplasia.
  • DISCUSSION: Management of fibrous dysplasia can be simple surveillance in the majority of patients.
  • Nevertheless, in the event of a single focus, particularly in a rib, fibrous dysplasia can raise a difficult problem of differential diagnosis with malignant tumors.

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  • (PMID = 18456067.001).
  • [ISSN] 0035-1040
  • [Journal-full-title] Revue de chirurgie orthopédique et réparatrice de l'appareil moteur
  • [ISO-abbreviation] Rev Chir Orthop Reparatrice Appar Mot
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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72. Flecher X, Casiraghi A, Aubaniac JM, Argenson JN: [Periacetabular osteotomy medium term survival in adult acetabular dysplasia]. Rev Chir Orthop Reparatrice Appar Mot; 2008 Jun;94(4):336-45

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Periacetabular osteotomy medium term survival in adult acetabular dysplasia].
  • [Transliterated title] Survie de l'ostéotomie périacétabulaire à moyen terme dans le traitement de la dysplasie acétabulaire de l'adulte.
  • PURPOSE OF THE STUDY: Acetabular dysplasia is a recognized cause of early onset degenerative hip disease.
  • Hips were classified with the Hip Study Group system as moderate dysplasia (VCE and VCA 25 degrees to 21 degrees ), severe dysplasia (20 degrees to 5 degrees ) and extreme dysplasia (less than 5 degrees ).
  • Several changes were made in the original technique: the three cuts were all done via the intrapelvic access; for severe and extreme dysplasia, a two thirds PAO was performed.
  • At the present time, the best indication appears to be young subjects (aged less than 30 years) with moderate to severe dysplasia, with no sign (even minimal) of intra-articular disorder or osteoarthritis.

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  • (PMID = 18555859.001).
  • [ISSN] 0035-1040
  • [Journal-full-title] Revue de chirurgie orthopédique et réparatrice de l'appareil moteur
  • [ISO-abbreviation] Rev Chir Orthop Reparatrice Appar Mot
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
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73. Wölner-Hanssen AB, Pozzi ECh, Vajtai I, Bornstein MM: [Interradicular course of the inferior alveolar nerve at the mandibular right third molar and monostotic fibrous dysplasia affecting the mandibular left third molar in the same patient. A case report]. Schweiz Monatsschr Zahnmed; 2009;119(5):489-502
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Interradicular course of the inferior alveolar nerve at the mandibular right third molar and monostotic fibrous dysplasia affecting the mandibular left third molar in the same patient. A case report].
  • [Transliterated title] Interradikulärer Verlauf des N. alveo- laris inferior bei 38 und apikale monostotische fibröse Dysplasie bei 48 beim selben Patienten. Ein Fallbericht.

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  • (PMID = 19579838.001).
  • [ISSN] 0256-2855
  • [Journal-full-title] Schweizer Monatsschrift fur Zahnmedizin = Revue mensuelle suisse d'odonto-stomatologie = Rivista mensile svizzera di odontologia e stomatologia
  • [ISO-abbreviation] Schweiz Monatsschr Zahnmed
  • [Language] FRE; GER
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Switzerland
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74. de Jong M, van Wijk JA, van der Hulst JP, Ludwig M, Bökenkamp A: [Schimke's immuno-osseous dysplasia as an explanation for the rare combination of disproportionately short stature and the nephrotic syndrome]. Ned Tijdschr Geneeskd; 2005 Sep 24;149(39):2178-82
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Schimke's immuno-osseous dysplasia as an explanation for the rare combination of disproportionately short stature and the nephrotic syndrome].
  • [Transliterated title] Immuno-ossale dysplasie van Schimke als zeldzame oorzaak van de combinatie van kleine lichaamslengte en nefrotisch syndroom.
  • The mild form of Schimke's immuno-osseous dysplasia was diagnosed as the common cause.
  • This rare, autosomal recessive osteochondrodysplasia is characterised by spondyloepiphyseal dysplasia, facial dysmorphism, T-cell immunodeficiency and progressive renal failure due to focal segmental glomerulosclerosis.
  • In Schimke's immuno-osseous dysplasia, a severe early-onset form and a milder later-onset form can be distinguished on the basis of the clinical course.

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  • (PMID = 16223078.001).
  • [ISSN] 0028-2162
  • [Journal-full-title] Nederlands tijdschrift voor geneeskunde
  • [ISO-abbreviation] Ned Tijdschr Geneeskd
  • [Language] dut
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Netherlands
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75. Ben hadj Hamida F, Jlaiel R, Ben Rayana N, Mahjoub H, Mellouli T, Ghorbel M, Krifa F: [Craniofacial fibrous dysplasia: a case report]. J Fr Ophtalmol; 2005 Oct;28(8):e6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Craniofacial fibrous dysplasia: a case report].
  • [Transliterated title] La dysplasie fibreuse cranio-faciale. A propos d'un cas.
  • Fibrous dysplasia is classified among benign bone tumors.
  • Fibrous dysplasia essentially affects children and young adults, with no sex preference.
  • We report an observation of craniofacial fibrous dysplasia affecting a child and discovery of proptosis, with no other ocular or general functional signs.
  • [MeSH-major] Facial Bones. Fibrous Dysplasia, Polyostotic / diagnosis. Skull

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  • (PMID = 16249758.001).
  • [ISSN] 1773-0597
  • [Journal-full-title] Journal français d'ophtalmologie
  • [ISO-abbreviation] J Fr Ophtalmol
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
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76. Ould Slimane M, Foulongne E, Derrey S, Fréger P, Proust F: [Polyostotic fibrous dysplasia of the thoracic spine. A case study and review of the literature]. Neurochirurgie; 2009 Dec;55(6):595-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Polyostotic fibrous dysplasia of the thoracic spine. A case study and review of the literature].
  • [Transliterated title] Dysplasie fibreuse polyostotique du rachis dorsal. Cas clinique et revue de la littérature.
  • Polyostotic fibrous dysplasia of the thoracic spine is extremely rare and considered a benign disease.
  • The diagnosis of fibrous dysplasia is usually made histologically on surgical biopsy but MRI and CT scan sometimes provide a preliminary indication.
  • [MeSH-major] Fibrous Dysplasia, Polyostotic / pathology. Spine / pathology

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  • (PMID = 19577779.001).
  • [ISSN] 1773-0619
  • [Journal-full-title] Neuro-Chirurgie
  • [ISO-abbreviation] Neurochirurgie
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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77. Flores Vivian G, Castro J, Verbeet T, Decoodt P: [A ventricle of all dangers: a clinical observation and evolution of a case of arrythmogenic right ventricular dysplasia]. Rev Med Brux; 2009 Sep-Oct;30(5):525-31
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  • [Title] [A ventricle of all dangers: a clinical observation and evolution of a case of arrythmogenic right ventricular dysplasia].
  • [Transliterated title] Un ventricule de tous les dangers: observation clinique et évolution d'un cas de dysplasie ventriculaire droite arythmogène.
  • Arrythmogenic right ventricular dysplasia (ARVD) is rare disease but it is a major cause of sudden death in young people and in athletes.
  • [MeSH-major] Arrhythmias, Cardiac / radiography. Arrhythmogenic Right Ventricular Dysplasia / radiography. Arrhythmogenic Right Ventricular Dysplasia / ultrasonography. Heart Ventricles / radiography

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  • (PMID = 19998800.001).
  • [ISSN] 0035-3639
  • [Journal-full-title] Revue médicale de Bruxelles
  • [ISO-abbreviation] Rev Med Brux
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Belgium
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78. Durand S, Hamcha H, Pannier S, Padovani JP, Finidori G, Glorion C: [Fibrous dysplasia of the proximal femur in children and teenagers: surgical results in 22 cases]. Rev Chir Orthop Reparatrice Appar Mot; 2007 Feb;93(1):17-22
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Fibrous dysplasia of the proximal femur in children and teenagers: surgical results in 22 cases].
  • [Transliterated title] La dysplasie fibreuse de l'extrémité proximale du fémur chez l'enfant et l'adolescent: résultats du traitement chirurgical dans 22 cas.
  • PURPOSE OF THE STUDY: Fibrous dysplasia is a rare benign bone tumor which occurs preferentially in the proximal femur.
  • The most common orthopedic problem is fibrous dysplasia of the proximal femur which generally requires surgical treatment.
  • MATERIAL AND METHODS: All children who underwent surgical treatment for fibrous dysplasia of the proximal femur between 1979 and 2001 were reviewed retrospectively.
  • [MeSH-major] Femur / surgery. Fibrous Dysplasia of Bone / surgery
  • [MeSH-minor] Adolescent. Adult. Bone Density Conservation Agents / therapeutic use. Bone Nails. Child. Child, Preschool. Cohort Studies. Curettage. Diphosphonates / therapeutic use. Female. Fibrous Dysplasia, Monostotic / surgery. Fibrous Dysplasia, Polyostotic / surgery. Humans. Internal Fixators. Male. Osteotomy / instrumentation. Osteotomy / methods. Retrospective Studies. Treatment Outcome

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  • (PMID = 17389820.001).
  • [ISSN] 0035-1040
  • [Journal-full-title] Revue de chirurgie orthopédique et réparatrice de l'appareil moteur
  • [ISO-abbreviation] Rev Chir Orthop Reparatrice Appar Mot
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Bone Density Conservation Agents; 0 / Diphosphonates
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79. Plat G, Rouquette I, Marcoux MO, Bloom MC, Acar P, Dulac Y: [Alveolar capillary dysplasia and persistent pulmonary hypertension of the newborn]. Arch Mal Coeur Vaiss; 2007 May;100(5):458-61
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Alveolar capillary dysplasia and persistent pulmonary hypertension of the newborn].
  • [Transliterated title] La dysplasie alvéolo-capillaire: une cause exceptionnelle d'hypertension artérielle pulmonaire persistante du nouveau né. A propos d'un cas.
  • Alveolar capillary dysplasia is a rare cause of persistent pulmonary hypertension of the newborn.
  • Echocardiography showed supra-systemic pulmonary hypertension with normal cardiac structure.
  • Autopsy revealed alveolar capillary dysplasia.

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  • (PMID = 17646774.001).
  • [ISSN] 0003-9683
  • [Journal-full-title] Archives des maladies du coeur et des vaisseaux
  • [ISO-abbreviation] Arch Mal Coeur Vaiss
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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80. Chelo D, Njiki Kinkela M, Monebenimp F, Nguefack S, Ngaha A, Tietche F: [Anhidrotic ectodermal dysplasia: report of one case at Mother and Child Center of Chantal Biya Foundation, Yaounde, Cameroon]. Pan Afr Med J; 2010;4:9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Anhidrotic ectodermal dysplasia: report of one case at Mother and Child Center of Chantal Biya Foundation, Yaounde, Cameroon].
  • [Transliterated title] La dysplasie ectodermique anhydrotique : à propos d'un cas au Centre Mère et Enfant de la Fondation Chantal Biya, Yaoundé, Cameroun.
  • Ectodermal dysplasia are rare genetic diseases characterized by the absence or dysplasia of some tissues of ectodermal origin.
  • We present a case of a young boy seen at the age of seven and a half years for late eruption of teeth, morphologic abnormalities of the teeth and a feeling of exaggerated heat.
  • The diagnosis of anhidrotic ectodermal dysplasia was discussed.
  • [MeSH-major] Ectodermal Dysplasia 1, Anhidrotic / complications. Ectodermal Dysplasia 3, Anhidrotic / complications. Tooth Abnormalities / etiology

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  • [Cites] J Med Genet. 1968 Dec;5(4):269-72 [5713637.001]
  • [Cites] Oral Surg Oral Med Oral Pathol. 1972 May;33(5):736-42 [4502148.001]
  • [Cites] Humangenetik. 1966;3(2):181-5 [5984977.001]
  • [Cites] Am J Med Genet. 1994 Nov 1;53(2):153-62 [7856640.001]
  • [Cites] Am J Med Genet. 1997 May 2;70(1):52-7 [9129742.001]
  • [Cites] Actual Odontostomatol (Paris). 1978 Mar;(121):95-106 [356530.001]
  • (PMID = 21119994.001).
  • [ISSN] 1937-8688
  • [Journal-full-title] The Pan African medical journal
  • [ISO-abbreviation] Pan Afr Med J
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Uganda
  • [Other-IDs] NLM/ PMC2984310
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81. Bacchetta J, Liutkus A, Dodat H, Cochat P, pour la Réunion pluridisciplinaire de diagnostic anténatal en néphro-urologie: [Multicystic dysplastic kidney disease: update and information for parents at the time of prenatal diagnosis]. Arch Pediatr; 2008 Jun;15(6):1107-15
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Multicystic dysplastic kidney disease: update and information for parents at the time of prenatal diagnosis].
  • [Transliterated title] Dysplasie rénale multikystique: mise au point et information pour les parents lors du diagnostic anténatal.
  • Multicystic kidney disease (MCKD) is the most common form of Congenital Abnormality of Kidney and Urinary Tract (CAKUT).
  • This anomaly of renal development is characterized by unilateral enlarged cystic formations and fibrous dysplastic parenchyma.
  • [MeSH-major] Multicystic Dysplastic Kidney / diagnosis. Prenatal Diagnosis

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  • (PMID = 18462928.001).
  • [ISSN] 0929-693X
  • [Journal-full-title] Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie
  • [ISO-abbreviation] Arch Pediatr
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article; Patient Education Handout
  • [Publication-country] France
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82. Jarreau PH, Fayon M, Baud O, Autret-Leca E, Danan M, de Verdelhan A, Castot A: [The use of postnatal corticosteroid therapy in premature infants to prevent or treat bronchopulmonary dysplasia: current situation and recommendations]. Arch Pediatr; 2010 Oct;17(10):1480-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [The use of postnatal corticosteroid therapy in premature infants to prevent or treat bronchopulmonary dysplasia: current situation and recommendations].
  • [Transliterated title] Utilisation de la corticothérapie postnatale chez le nouveau-né prématuré dans la prévention et le traitement de la dysplasie bronchopulmonaire : état des lieux et conduite à tenir.
  • In the last few years, several studies related to the benefit/risk balance of postnatal corticosteroids administered to premature neonates for prevention or treatment of bronchopulmonary dysplasia (BPD) have been published.
  • [MeSH-major] Adrenal Cortex Hormones / therapeutic use. Bronchopulmonary Dysplasia / drug therapy. Infant, Premature, Diseases / drug therapy

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  • [Copyright] Copyright © 2010. Published by Elsevier SAS.. All rights reserved.
  • (PMID = 20864322.001).
  • [ISSN] 1769-664X
  • [Journal-full-title] Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie
  • [ISO-abbreviation] Arch Pediatr
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Adrenal Cortex Hormones; 9842X06Q6M / Betamethasone; WI4X0X7BPJ / Hydrocortisone
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83. Xiaojing H, Jiannong Z, Weibo X: [The utility of magnetic resonance imaging in the evaluation of arrhythmogenic right ventricular cardiomyopathy]. J Radiol; 2009 Jun;90(6):717-23
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Utilité de l'imagerie par résonance magnétique nucléaire dans l'évaluation de la dysplasie ventriculaire droite arythmogène.
  • [MeSH-major] Arrhythmogenic Right Ventricular Dysplasia / diagnosis. Image Enhancement. Image Processing, Computer-Assisted. Magnetic Resonance Imaging. Magnetic Resonance Imaging, Cine. Oxygen Consumption / physiology


84. Puri RD, Thakur S, Verma IC: Spectrum of severe skeletal dysplasias in North India. Indian J Pediatr; 2007 Nov;74(11):995-1002

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Spectrum of severe skeletal dysplasias in North India.
  • OBJECTIVE: Severe skeletal dysplasias are a group of bone growth disorders characterized by a lethal outcome in utero or infancy.
  • We describe our experience of the severe skeletal dysplasias diagnosed amongst fetal autopsies done at a tertiary level centre over a five year period.
  • RESULTS: Short rib dysplasia syndromes with or without polydactyly, osteogenesis imperfecta type II, thanatophoric dysplasia, campomelic dysplasia, chondrodysplasia punctata, rhizomelic type and achondrogenesis were the lethal skeletal dysplasias diagnosed.
  • CONCLUSION: Precise identification of the tye of skeletal dysplasia is paramount for proper genetic counseling.
  • Postnatal examination and detailed radiographic examination of the fetus especially of the pelvis, limbs, skull and spine are essential to identify the type of skeletal dysplasia.

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  • (PMID = 18057679.001).
  • [ISSN] 0973-7693
  • [Journal-full-title] Indian journal of pediatrics
  • [ISO-abbreviation] Indian J Pediatr
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
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85. Dornacher D, Cakir B, Reichel H, Nelitz M: [Reliability of digital measurement of acetabular index in hip dysplasia to the time children start walking]. Z Orthop Unfall; 2008 Mar-Apr;146(2):246-50

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Reliability of digital measurement of acetabular index in hip dysplasia to the time children start walking].
  • AIM: An assessment of the reproducibility of the acetabular index on the basis of anteroposterior radiographs of the pelvis was performed in order to rule out residual dysplasia of the hip in the second year of life.
  • METHOD: 51 consecutive patients (41 girls, 10 boys) with congenital dysplasia of the hip (35 bilateral, 16 unilateral) were included.
  • Acetabular indices were measured bilaterally and blinded by two observers (O1 and O2), then classified according to the normal values of the hip joint described by Tönnis et al. (normal = lower single standard deviation [s], light dysplasia = above single standard deviation [s - 2 s] and severe dysplasie = above double standard deviation [2 s]).
  • CONCLUSION: The reproducibility of radiological surveillance in congenital hip dysplasia, approximately to the time children start walking, can be considered as adequate.
  • In spite of good statistical values for reliability, decreasing accuracy in classifying into Tönnis' normal values of the hip joint is seen with increasing degree of dysplasia.

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  • (PMID = 18404590.001).
  • [ISSN] 1864-6697
  • [Journal-full-title] Zeitschrift für Orthopädie und Unfallchirurgie
  • [ISO-abbreviation] Z Orthop Unfall
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
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86. Mazurkiewicz-Bełdzińska M, Szmuda M, Matheisel A: Correlation of neuroradiological, electroencephalographic and clinical findings in cortical dysplasias in children. Folia Neuropathol; 2006;44(4):314-8
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  • [Title] Correlation of neuroradiological, electroencephalographic and clinical findings in cortical dysplasias in children.
  • INTRODUCTION: Cortical dysplasias (CD) are defined as malformations of cortical development.
  • Recognition of the importance of cortical dysplasias has been shown in many studies when introducing structural MRI.
  • The following study was performed in order to correlate the neuroimaging findings with the electroencephalographic and clinical picture of children with cortical dysplasias.
  • RESULTS: There were 31 patients with focal dysplasias, 6 with schizencephaly, 4 with heterotopias, 3 lissencephaly and 2 with band heterotopia.
  • 74% of patients were mentally retarded and 30% had focal neurological deficits.

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  • (PMID = 17183458.001).
  • [ISSN] 1641-4640
  • [Journal-full-title] Folia neuropathologica
  • [ISO-abbreviation] Folia Neuropathol
  • [Language] ENG
  • [Publication-type] Journal Article
  • [Publication-country] Poland
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87. Patel MM, Wilkey JF, Abdelsayed R, D'Silva NJ, Malchoff C, Mallya SM: Analysis of GNAS mutations in cemento-ossifying fibromas and cemento-osseous dysplasias of the jaws. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2010 May;109(5):739-43
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Analysis of GNAS mutations in cemento-ossifying fibromas and cemento-osseous dysplasias of the jaws.
  • OBJECTIVES: It is well established that fibrous dysplasia (FD) is caused by mutations of the Arg(201) codon of the GNAS gene.
  • However, the role of GNAS mutation in the pathogenesis of cement-osseous dysplasias (COD) and cemento-ossifying fibromas (COF) is not fully known.

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  • [Copyright] Copyright (c) 2010 Mosby, Inc. All rights reserved.
  • [Cites] J Bone Miner Res. 2000 Jan;15(1):120-8 [10646121.001]
  • [Cites] Histopathology. 2009 Mar;54(4):401-18 [18637149.001]
  • [Cites] Acta Biomed Ateneo Parmense. 1999;70(1-2):5-11 [11402810.001]
  • [Cites] J Bone Miner Res. 2001 Sep;16(9):1710-8 [11547842.001]
  • [Cites] Nat Genet. 2002 Dec;32(4):676-80 [12434154.001]
  • [Cites] Clin Nucl Med. 2003 May;28(5):416-8 [12702945.001]
  • [Cites] J Clin Endocrinol Metab. 2003 Sep;88(9):4413-7 [12970318.001]
  • [Cites] Nucleic Acids Res. 2004;32(7):e63 [15096559.001]
  • [Cites] N Engl J Med. 1991 Dec 12;325(24):1688-95 [1944469.001]
  • [Cites] Arch Pathol Lab Med. 1993 Mar;117(3):284-90 [8442673.001]
  • [Cites] J Oral Maxillofac Surg. 1993 Aug;51(8):828-35 [8336219.001]
  • [Cites] J Clin Endocrinol Metab. 1994 Mar;78(3):803-6 [8126161.001]
  • [Cites] Am J Pathol. 1994 Dec;145(6):1301-8 [7992835.001]
  • [Cites] Am J Surg Pathol. 1995 Jul;19(7):775-81 [7793475.001]
  • [Cites] Bone. 1997 Aug;21(2):201-6 [9267696.001]
  • [Cites] J Neurosurg. 2005 Jun;102(6):1151-4 [16028779.001]
  • [Cites] J Bone Joint Surg Am. 2005 Aug;87(8):1848-64 [16085630.001]
  • [Cites] J Bone Miner Res. 2006 Dec;21 Suppl 2:P114-9 [17228999.001]
  • [Cites] J Bone Miner Res. 2006 Dec;21 Suppl 2:P120-4 [17229000.001]
  • [Cites] Mod Pathol. 2007 Mar;20(3):389-96 [17334331.001]
  • [Cites] J Bone Miner Res. 2007 Sep;22(9):1468-74 [17501668.001]
  • [Cites] QJM. 2001 Apr;94(4):213-22 [11294964.001]
  • (PMID = 20346714.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] ENG
  • [Grant] United States / NIDCR NIH HHS / DE / DE007302-11; United States / NIDCR NIH HHS / DE / T32 DE007302; United States / NIDCR NIH HHS / DE / DE014773-05; United States / NIDCR NIH HHS / DE / K22 DE014773; United States / NIDCR NIH HHS / DE / T32 DE007302-11; United States / NIDCR NIH HHS / DE / K22 DE014773-05
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Codon; 0 / DNA Primers; 0 / DNA, Neoplasm; 4QD397987E / Histidine; 94ZLA3W45F / Arginine; EC 3.6.1.- / GNAS protein, human; EC 3.6.5.1 / GTP-Binding Protein alpha Subunits, Gs
  • [Other-IDs] NLM/ NIHMS165413; NLM/ PMC2860034
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88. Krakow D, Lachman RS, Rimoin DL: Guidelines for the prenatal diagnosis of fetal skeletal dysplasias. Genet Med; 2009 Feb;11(2):127-33
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Guidelines for the prenatal diagnosis of fetal skeletal dysplasias.
  • The osteochondrodysplasias, or skeletal dysplasias are a genetically heterogeneous group of over 350 distinct disorders, and many of them can present in the prenatal period as demonstrated by ultrasound.
  • These guidelines provide an approach to a fetus suspected of manifesting a skeletal dysplasia.

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  • [Cites] Annu Rev Cell Dev Biol. 2000;16:191-220 [11031235.001]
  • [Cites] Pediatrics. 2007 Aug;120(2):e436-41 [17671048.001]
  • [Cites] Am J Med Genet. 2001 Nov 22;104(2):140-6 [11746045.001]
  • [Cites] Am J Med Genet. 2001 Winter;106(4):282-93 [11891680.001]
  • [Cites] Am J Med Genet. 2002 Nov 15;113(1):65-77 [12400068.001]
  • [Cites] J Ultrasound Med. 2003 Mar;22(3):255-8; quiz 259-61 [12636325.001]
  • [Cites] Ultrasound Obstet Gynecol. 2003 May;21(5):467-72 [12768559.001]
  • [Cites] Birth Defects Res C Embryo Today. 2003 May;69(2):93-101 [12955855.001]
  • [Cites] Hum Genet. 2003 Oct;113(5):447-51 [12938037.001]
  • [Cites] Obstet Gynecol. 1986 Jan;67(1):74-8 [3940342.001]
  • [Cites] J Med Genet. 1986 Aug;23(4):328-32 [3746832.001]
  • [Cites] Obstet Gynecol Surv. 1987 Apr;42(4):199-217 [3554053.001]
  • [Cites] Obstet Gynecol. 1988 Aug;72(2):181-4 [3292975.001]
  • [Cites] Am J Obstet Gynecol. 1993 Sep;169(3):668-75 [8372878.001]
  • [Cites] Am J Med Genet. 1996 Jan 2;61(1):49-58 [8741918.001]
  • [Cites] Am J Obstet Gynecol. 1996 Aug;175(2):477-83 [8765272.001]
  • [Cites] Am J Med Genet. 1996 Nov 11;65(4):259-65 [8923931.001]
  • [Cites] Ultrasound Obstet Gynecol. 1997 Jun;9(6):392-7 [9239824.001]
  • [Cites] Am J Obstet Gynecol. 1997 Oct;177(4):864-9 [9369835.001]
  • [Cites] Am J Med Genet. 1998 Feb 17;75(5):518-22 [9489797.001]
  • [Cites] Prenat Diagn. 1998 Apr;18(4):357-62 [9602482.001]
  • [Cites] Pediatr Radiol. 1999 May;29(5):322 [10382206.001]
  • [Cites] BJOG. 2006 Jun;113(6):664-74 [16709209.001]
  • [Cites] Am J Med Genet A. 2007 Jan 1;143A(1):1-18 [17120245.001]
  • [Cites] Clin Obstet Gynecol. 2007 Jun;50(2):478-86 [17513933.001]
  • [Cites] Ann Genet. 2000 Jul-Dec;43(3-4):163-9 [11164199.001]
  • (PMID = 19265753.001).
  • [ISSN] 1530-0366
  • [Journal-full-title] Genetics in medicine : official journal of the American College of Medical Genetics
  • [ISO-abbreviation] Genet. Med.
  • [Language] ENG
  • [Grant] United States / NCRR NIH HHS / RR / M01-RR00425; United States / NICHD NIH HHS / HD / HD022657-23S10001; United States / NICHD NIH HHS / HD / HD022657-23S1; United States / NICHD NIH HHS / HD / P01 HD022657; United States / NICHD NIH HHS / HD / HD022657-230001; None / None / / P01 HD022657-23; United States / NICHD NIH HHS / HD / HD022657-239001; United States / NICHD NIH HHS / HD / HD22657; United States / NICHD NIH HHS / HD / P01 HD022657-230001; United States / NICHD NIH HHS / HD / P01 HD022657-239001; United States / NICHD NIH HHS / HD / P01 HD022657-23S10001; United States / NICHD NIH HHS / HD / P01 HD022657-23; United States / NCRR NIH HHS / RR / M01 RR000425; United States / NICHD NIH HHS / HD / P01 HD022657-23S1
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Other-IDs] NLM/ NIHMS177770; NLM/ PMC2832320
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89. Tsui IF, Poh CF, Garnis C, Rosin MP, Zhang L, Lam WL: Multiple pathways in the FGF signaling network are frequently deregulated by gene amplification in oral dysplasias. Int J Cancer; 2009 Nov 1;125(9):2219-28
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple pathways in the FGF signaling network are frequently deregulated by gene amplification in oral dysplasias.
  • Here, we evaluated 50 high-grade dysplasias and low-grade dysplasias that later progressed to cancer for gene dosage aberrations using tiling-path DNA microarrays.
  • No such alterations were found in 14 low-grade dysplasias that did not progress, whereas 43.5% (10/23) of OSCCs were found to have altered genes within the pathways with DNA amplification.
  • Multitarget FISH showed that amplification of EGFR and CCND1 can coexist in single cells of an oral dysplasia, suggesting the dependence on multiple oncogenes for OPL progression.

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  • [Copyright] (c) 2009 UICC.
  • [Cites] Cancer Res. 2009 Mar 15;69(6):2568-76 [19276369.001]
  • [Cites] Cancer Res. 2000 Jul 15;60(14):3893-8 [10919665.001]
  • [Cites] Oral Oncol. 2009 Apr-May;45(4-5):324-34 [18805044.001]
  • [Cites] Clin Cancer Res. 2000 Feb;6(2):357-62 [10690511.001]
  • [Cites] Bioinformatics. 2009 May 1;25(9):1099-104 [19276148.001]
  • [Cites] Cancer Res. 2000 Nov 1;60(21):6116-33 [11085536.001]
  • [Cites] Genome Biol. 2001;2(3):REVIEWS3005 [11276432.001]
  • [Cites] Nat Rev Cancer. 2002 Jul;2(7):489-501 [12094235.001]
  • [Cites] Science. 2002 Jul 5;297(5578):63-4 [12098689.001]
  • [Cites] Cancer Res. 2002 Nov 15;62(22):6447-50 [12438233.001]
  • [Cites] J Mol Diagn. 2003 May;5(2):103-12 [12707375.001]
  • [Cites] Cancer Res. 2003 Dec 15;63(24):8582-5 [14695166.001]
  • [Cites] Cancer Res. 2004 Jan 1;64(1):55-63 [14729608.001]
  • [Cites] Nat Genet. 2004 Mar;36(3):299-303 [14981516.001]
  • [Cites] Oncogene. 2004 Apr 1;23(14):2484-98 [14676830.001]
  • [Cites] Neoplasia. 2004 Jan-Feb;6(1):1-6 [15068665.001]
  • [Cites] Cancer Cell. 2004 Apr;5(4):311-6 [15093538.001]
  • [Cites] Cancer Cell. 2004 May;5(5):489-500 [15144956.001]
  • [Cites] Mol Cancer. 2004 Mar 22;3:9 [15035667.001]
  • [Cites] Cancer Genet Cytogenet. 2004 Oct 1;154(1):27-35 [15381369.001]
  • [Cites] J Oral Surg. 1977 Sep;35(9):756-62 [267762.001]
  • [Cites] Oral Surg Oral Med Oral Pathol. 1978 Oct;46(4):518-39 [280847.001]
  • [Cites] Arch Pathol Lab Med. 1981 Jan;105(1):15-9 [6893909.001]
  • [Cites] J Clin Invest. 1987 Jun;79(6):1629-34 [3034978.001]
  • [Cites] Mutat Res. 1989 May;219(3):171-8 [2567961.001]
  • [Cites] Am J Surg Pathol. 1989;13 Suppl 1:5-16 [2699168.001]
  • [Cites] Genes Chromosomes Cancer. 1995 Apr;12(4):288-95 [7539284.001]
  • [Cites] Nat Genet. 1995 Oct;11(2):210-2 [7550353.001]
  • [Cites] Science. 1996 Jan 19;271(5247):350-3 [8553070.001]
  • [Cites] Nat Med. 1996 Jun;2(6):682-5 [8640560.001]
  • [Cites] Dermatol Clin. 1996 Apr;14(2):205-23 [8725579.001]
  • [Cites] Science. 1997 Mar 28;275(5308):1943-7 [9072974.001]
  • [Cites] Cancer Cell. 2004 Nov;6(5):433-8 [15542426.001]
  • [Cites] BMC Bioinformatics. 2005;6:274 [16297240.001]
  • [Cites] Oncogene. 2006 Apr 20;25(17):2558-64 [16314836.001]
  • [Cites] Cancer Res. 2005 Sep 1;65(17):7561-7 [16140918.001]
  • [Cites] Cancer. 2005 Dec 1;104(11):2430-6 [16245318.001]
  • [Cites] Genes Chromosomes Cancer. 2006 Feb;45(2):118-25 [16235239.001]
  • [Cites] Lancet Oncol. 2005 May;6(5):279-86 [15863375.001]
  • [Cites] Oncogene. 2005 Jun 16;24(26):4232-42 [15824737.001]
  • [Cites] Br J Cancer. 2006 Jun 19;94(12):1927-35 [16705311.001]
  • [Cites] Trends Genet. 2006 Aug;22(8):447-55 [16787682.001]
  • [Cites] J Pathol. 2006 Sep;210(1):67-74 [16767698.001]
  • [Cites] Oncogene. 2006 Sep 7;25(40):5517-26 [16619035.001]
  • [Cites] Cancer Biol Ther. 2006 Sep;5(9):1059-64 [16940750.001]
  • [Cites] Oncogene. 2006 Nov 23;25(55):7324-32 [16751803.001]
  • [Cites] Genes Chromosomes Cancer. 2007 Feb;46(2):143-54 [17099871.001]
  • [Cites] Am J Hum Genet. 2007 Jan;80(1):91-104 [17160897.001]
  • [Cites] Semin Cancer Biol. 2007 Feb;17(1):42-55 [17161620.001]
  • [Cites] Oral Oncol. 2007 Jan;43(1):60-6 [16807070.001]
  • [Cites] Oral Oncol. 2007 May;43(5):508-14 [17005439.001]
  • [Cites] Genomics. 2007 May;89(5):647-53 [17276656.001]
  • [Cites] Oncogene. 2007 May 14;26(22):3113-21 [17496910.001]
  • [Cites] Cancer Res. 2007 May 15;67(10):4605-19 [17510386.001]
  • [Cites] J Clin Oncol. 2007 Jun 1;25(16):2164-70 [17538160.001]
  • [Cites] Annu Rev Genet. 2007;41:41-61 [17550342.001]
  • [Cites] J Oral Pathol Med. 2008 Mar;37(3):127-33 [18251935.001]
  • [Cites] BMC Genomics. 2008;9:69 [18254958.001]
  • [Cites] J Can Dent Assoc. 2008 Apr;74(3):283-8 [18387269.001]
  • [Cites] Cancer Res. 2008 May 1;68(9):3099-107 [18451134.001]
  • [Cites] BMC Bioinformatics. 2008;9:243 [18492270.001]
  • [Cites] Can Fam Physician. 2008 Jun;54(6):870-5 [18556495.001]
  • [Cites] Cancer Res. 2008 Jul 1;68(13):5067-75 [18593905.001]
  • [Cites] Oncogene. 2008 Jul 31;27(33):4615-24 [18391978.001]
  • [Cites] Cancer Epidemiol Biomarkers Prev. 2008 Aug;17(8):2174-9 [18708411.001]
  • [Cites] J Proteome Res. 2009 Jan;8(1):300-9 [19072117.001]
  • [Cites] Cancer Prev Res (Phila). 2008 Nov;1(6):424-9 [19138989.001]
  • [Cites] J Cancer Res Clin Oncol. 2009 Mar;135(3):395-402 [18813952.001]
  • [Cites] Int J Cancer. 2009 Apr 15;124(8):1778-84 [19117057.001]
  • (PMID = 19623652.001).
  • [ISSN] 1097-0215
  • [Journal-full-title] International journal of cancer
  • [ISO-abbreviation] Int. J. Cancer
  • [Language] ENG
  • [Grant] United States / NIDCR NIH HHS / DE / R01DE15965; United States / NIDCR NIH HHS / DE / DE017013-04; United States / NIDCR NIH HHS / DE / R01 DE017013-04; United States / NIDCR NIH HHS / DE / R01 DE013124; United States / NIDCR NIH HHS / DE / R01 DE015965; United States / NIDCR NIH HHS / DE / R01DE13124; United States / NIDCR NIH HHS / DE / R01 DE017013
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / CCND1 protein, human; 0 / RNA, Messenger; 136601-57-5 / Cyclin D1; 62031-54-3 / Fibroblast Growth Factors; EC 2.7.10.1 / Receptor, Epidermal Growth Factor
  • [Other-IDs] NLM/ NIHMS132913; NLM/ PMC2761835
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90. Faden MA, Krakow D, Ezgu F, Rimoin DL, Lachman RS: The Erlenmeyer flask bone deformity in the skeletal dysplasias. Am J Med Genet A; 2009 Jun;149A(6):1334-45
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] The Erlenmeyer flask bone deformity in the skeletal dysplasias.
  • Erlenmeyer flask bone deformity (EFD) is a long-standing term used to describe a specific abnormality of the distal femora.
  • The deformity consists of lack of modeling of the di-metaphysis with abnormal cortical thinning and lack of the concave di-metaphyseal curve resulting in an Erlenmeyer flask-like appearance.
  • We interrogated the International Skeletal Dysplasia Registry (ISDR) radiographic database (1988-2007) to determine which skeletal dysplasias or syndromes were highly associated with EFD, whether it was a uniform finding in these disorders, and if forms of EFD could be differentiated.
  • EFD-T was identified in: frontometaphyseal dysplasia, craniometaphyseal dysplasia, craniodiaphyseal dysplasia, diaphyseal dysplasia-Engelmann type, metaphyseal dysplasia-Pyle type, Melnick-Needles osteodysplasty, and otopalatodigital syndrome type I.
  • The second group was the atypical type (EFD-A) due to absence of normal di-metaphyseal modeling with abnormal radiographic appearance of trabecular bone and was seen in dysosteosclerosis and osteopetrosis.
  • The third group was EFD-marrow expansion type (EFD-ME) in which bone marrow hyperplasia or infiltration leads to abnormal modeling (e.g., Gaucher disease).

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  • [Copyright] (c) 2009 Wiley-Liss, Inc.
  • [Cites] AMA Arch Intern Med. 1954 Dec;94(6):871-85 [13217486.001]
  • [Cites] Medicine (Baltimore). 1958 Feb;37(1):1-95 [13516139.001]
  • [Cites] Am J Roentgenol Radium Ther Nucl Med. 1961 Apr;85:680-4 [13705274.001]
  • [Cites] Fortschr Geb Rontgenstr Nuklearmed. 1961 Jun;94:702-12 [13760661.001]
  • [Cites] Hum Genet. 1982;60(1):36-41 [7076246.001]
  • [Cites] Skeletal Radiol. 1982;8(1):51-4 [7079784.001]
  • [Cites] Helv Paediatr Acta. 1982 May;37(2):151-60 [7096116.001]
  • [Cites] Am J Med Genet. 1982 Sep;13(1):71-9 [7137223.001]
  • [Cites] Am J Med Genet. 2000 Feb 28;90(5):407-22 [10706363.001]
  • [Cites] Am J Med Genet. 2000 Mar 13;91(2):153-6 [10748417.001]
  • [Cites] Am J Med Genet. 2000 May 29;92(3):191-4 [10817653.001]
  • [Cites] Am J Med Genet. 2000 Dec 18;95(5):482-91 [11146471.001]
  • [Cites] Respir Med. 2000 Dec;94(12):1241-51 [11192962.001]
  • [Cites] Nat Genet. 2001 May;28(1):37-41 [11326272.001]
  • [Cites] Am J Med Genet. 2001 Jun 1;101(1):74-7 [11343343.001]
  • [Cites] Med Pediatr Oncol. 2001 Jun;36(6):657-8 [11344501.001]
  • [Cites] Ann Hematol. 2001 Oct;80(10):620-2 [11732877.001]
  • [Cites] Br J Radiol. 2002;75 Suppl 1:A2-12 [12036828.001]
  • [Cites] Rheumatol Int. 2002 Jul;22(3):116-8 [12111087.001]
  • [Cites] J Med Genet. 2002 Aug;39(8):603-7 [12161605.001]
  • [Cites] Am J Med Genet. 2002 Aug 1;111(2):205-9 [12210352.001]
  • [Cites] Nat Genet. 2003 Apr;33(4):487-91 [12612583.001]
  • [Cites] Cell Mol Neurobiol. 2004 Feb;24(1):1-24 [15049507.001]
  • [Cites] Am J Med Genet A. 2004 Jul 15;128A(2):204-8 [15214018.001]
  • [Cites] Minerva Pediatr. 2004 Feb;56(1):115-8 [15249921.001]
  • [Cites] Am J Roentgenol Radium Ther Nucl Med. 1967 Mar;99(3):712-6 [6020650.001]
  • [Cites] Fortschr Geb Rontgenstr Nuklearmed. 1968 Oct;109(4):504-12 [5750745.001]
  • [Cites] Am J Dis Child. 1969 Sep;118(3):487-94 [5807657.001]
  • [Cites] J Bone Joint Surg Am. 1970 Mar;52(2):347-54 [5440013.001]
  • [Cites] Am J Dis Child. 1972 Mar;123(3):254-8 [5026209.001]
  • [Cites] Acta Chir Orthop Traumatol Cech. 1972 Mar;39(2):98-104 [5039723.001]
  • [Cites] Radiology. 1973 Sep;108(3):659-64 [4723667.001]
  • [Cites] Birth Defects Orig Artic Ser. 1974;10(12):61-71 [4461093.001]
  • [Cites] S Afr Med J. 1975 May 17;49(21):839-42 [1135718.001]
  • [Cites] Am J Pathol. 1975 Aug;80(2):309-16 [169701.001]
  • [Cites] J Bone Joint Surg Am. 1977 Sep;59(6):802-9 [908704.001]
  • [Cites] J Bone Joint Surg Am. 1978 Apr;60(3):392-4 [649644.001]
  • [Cites] AJR Am J Roentgenol. 1986 Feb;146(2):245-7 [3484570.001]
  • [Cites] Clin Genet. 1986 Nov;30(5):381-91 [3802557.001]
  • [Cites] J Pediatr. 1988 Dec;113(6):1078-82 [3193315.001]
  • [Cites] Z Rheumatol. 1989 Nov-Dec;48(6):326-30 [2623978.001]
  • [Cites] Arch Dis Child. 1963 Feb;38:86-8 [13930991.001]
  • [Cites] J Pediatr. 1963 Jul;63:69-75 [13949300.001]
  • [Cites] Am J Roentgenol Radium Ther Nucl Med. 1960 Sep;84:461-6 [14444047.001]
  • [Cites] Clin Radiol. 2006 Jan;61(1):40-52 [16356815.001]
  • [Cites] J Perinatol. 2006 Jun;26(6):371-4 [16724078.001]
  • [Cites] Am J Med Genet A. 2006 Jun 1;140(11):1234-7 [16691581.001]
  • [Cites] Eur J Hum Genet. 2007 Jan;15(1):3-9 [16926860.001]
  • [Cites] Clin Orthop Relat Res. 2007 Jan;454:262-9 [16906106.001]
  • [Cites] Environ Health Perspect. 2007 Mar;115(3):463-71 [17431500.001]
  • [Cites] Br J Surg. 1949 Jul;37(145):52-63 [18135657.001]
  • [Cites] Br J Radiol. 1948 May;21(245):236-41 [18859677.001]
  • [Cites] Am J Dis Child. 1972 Jul;124(1):111-5 [5033742.001]
  • [Cites] Clin Orthop Relat Res. 1978 Nov-Dec;(137):208-14 [743830.001]
  • [Cites] Br J Radiol. 1979 Jun;52(618):431-40 [465917.001]
  • [Cites] Dev Med Child Neurol. 1980 Feb;22(1):72-84 [7358236.001]
  • [Cites] Am J Med. 1980 Jul;69(1):64-74 [7386510.001]
  • [Cites] Am J Med Genet. 1980;5(1):43-55 [7395899.001]
  • [Cites] Nephron. 1981;28(6):268-72 [7312081.001]
  • [Cites] Skeletal Radiol. 1991;20(1):37-41 [2000503.001]
  • [Cites] Radiology. 1992 Apr;183(1):129-35 [1549658.001]
  • [Cites] Radiology. 1993 May;187(2):489-92 [8475296.001]
  • [Cites] Clin Orthop Relat Res. 1993 Sep;(294):45-51 [8358946.001]
  • [Cites] Genet Couns. 1995;6(3):233-40 [8588852.001]
  • [Cites] Clin Exp Dermatol. 1996 Jul;21(4):269-72 [8959896.001]
  • [Cites] Br J Haematol. 1998 Dec;103(4):897-901 [9886298.001]
  • [Cites] Am J Med Genet. 1999 Aug 6;85(4):395-402 [10398267.001]
  • [Cites] Eur Cytokine Netw. 1999 Jun;10(2):205-10 [10400826.001]
  • (PMID = 19444897.001).
  • [ISSN] 1552-4833
  • [Journal-full-title] American journal of medical genetics. Part A
  • [ISO-abbreviation] Am. J. Med. Genet. A
  • [Language] ENG
  • [Grant] None / None / / P01 HD022657-23; United States / NICHD NIH HHS / HD / HD 22567; United States / NICHD NIH HHS / HD / P01 HD022657-23
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] United States
  • [Number-of-references] 80
  • [Other-IDs] NLM/ NIHMS178279; NLM/ PMC2836257
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91. Furuichi T, Kayserili H, Hiraoka S, Nishimura G, Ohashi H, Alanay Y, Lerena JC, Aslanger AD, Koseki H, Cohn DH, Superti-Furga A, Unger S, Ikegawa S: Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseases. J Med Genet; 2009 Aug;46(8):562-8
SciCrunch. KEGG: Data: Disease Annotation .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseases.
  • BACKGROUND: Schneckenbecken dysplasia (SBD) is an autosomal recessive lethal skeletal dysplasia that is classified into the severe spondylodysplastic dysplasias (SSDD) group in the international nosology for skeletal dysplasias.
  • OBJECT: To explore further the range of SLC35D1 mutations in SBD and elucidate whether SLC35D1 mutations cause other skeletal dysplasias that belong to the SSDD group.
  • METHODS AND RESULTS: We searched for SLC35D1 mutations in five families with SBD and 15 patients with other SSDD group diseases, including achodrogenesis type 1A, spondylometaphyseal dysplasia Sedaghatian type and fibrochondrogenesis.

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  • [Cites] FEBS Lett. 2001 Apr 20;495(1-2):87-93 [11322953.001]
  • [Cites] Nat Med. 2007 Nov;13(11):1363-7 [17952091.001]
  • [Cites] Pflugers Arch. 2004 Feb;447(5):768-75 [12759756.001]
  • [Cites] Am J Med Genet. 1980;6(4):269-74 [7211944.001]
  • [Cites] Am J Med Genet. 1984 Oct;19(2):265-75 [6507478.001]
  • [Cites] Am J Med Genet. 1986 Sep;25(1):47-59 [3799723.001]
  • [Cites] J Pediatr. 1988 Jan;112(1):23-31 [3275766.001]
  • [Cites] Pediatr Radiol. 2001 Jan;31(1):27-30 [11200994.001]
  • [Cites] Hum Mutat. 2001 Mar;17(3):159-71 [11241838.001]
  • [Cites] Skeletal Radiol. 1991;20(7):534-8 [1754916.001]
  • [Cites] Nat Genet. 1996 Jan;12(1):100-2 [8528239.001]
  • [Cites] Am J Hum Genet. 1996 Feb;58(2):255-62 [8571951.001]
  • [Cites] Hum Genet. 1996 Jul;98(1):102-8 [8682493.001]
  • [Cites] J Comput Biol. 1997 Fall;4(3):311-23 [9278062.001]
  • [Cites] J Biochem. 1998 May;123(5):912-7 [9562625.001]
  • [Cites] Matrix Biol. 1998 Oct;17(5):361-9 [9822202.001]
  • [Cites] Hum Genet. 1999 May;104(5):435-7 [10394938.001]
  • [Cites] J Biochem. 1999 Jul;126(1):68-77 [10393322.001]
  • [Cites] Genomics. 2005 Jan;85(1):106-16 [15607426.001]
  • [Cites] Genome Res. 2006 Jan;16(1):97-105 [16344554.001]
  • [Cites] Am J Med Genet A. 2007 Jan 1;143A(1):1-18 [17120245.001]
  • [Cites] J Med Genet. 2007 Apr;44(4):e73 [17400792.001]
  • [Cites] J Biol Chem. 2007 Aug 24;282(34):24615-22 [17599910.001]
  • [Cites] Eur J Biochem. 2002 Jan;269(1):128-38 [11784306.001]
  • (PMID = 19508970.001).
  • [ISSN] 1468-6244
  • [Journal-full-title] Journal of medical genetics
  • [ISO-abbreviation] J. Med. Genet.
  • [Language] eng
  • [Grant] United States / NICHD NIH HHS / HD / P01 HD022657; United States / NICHD NIH HHS / HD / P01 HD022657-25
  • [Publication-type] Case Reports; Letter; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Monosaccharide Transport Proteins; 0 / Nucleotides; 0 / SLC35D1 protein, human
  • [Other-IDs] NLM/ NIHMS297015; NLM/ PMC4144354
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92. Torres-Rendon A, Stewart R, Craig GT, Wells M, Speight PM: DNA ploidy analysis by image cytometry helps to identify oral epithelial dysplasias with a high risk of malignant progression. Oral Oncol; 2009 Jun;45(6):468-73
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] DNA ploidy analysis by image cytometry helps to identify oral epithelial dysplasias with a high risk of malignant progression.
  • Abnormal DNA content (aneuploidy) has been associated with malignant and premalignant epithelial lesions.
  • The presence of aneuploidy in tumours at an early stage and in dysplastic lesions suggests that analysis of DNA content may be a useful marker for determination of prognosis in these lesions.
  • The aim of this study was to use DNA image cytometry to evaluate aneuploidy in oral dysplastic lesions and to determine whether aneuploidy is associated with malignant progression.
  • Forty-two lesions of oral epithelial dysplasias (OED) that had progressed to oral squamous cell carcinoma (OSCC) and 44 lesions that did not progress were analysed for DNA ploidy using image cytometry of nuclear monolayers prepared from paraffin-embedded tissue.
  • A total of 19 OED were aneuploid of which 74% showed malignant progression compared to only 42% of the diploid lesions.
  • The PPV and NPV were 0.74 and 0.58.
  • We conclude that aneuploid oral dysplastic lesions have a high risk of malignant progression and that DNA image cytometry might help to identify those lesions most at risk.

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  • (PMID = 18805043.001).
  • [ISSN] 1879-0593
  • [Journal-full-title] Oral oncology
  • [ISO-abbreviation] Oral Oncol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
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93. Torres-Rendon A, Roy S, Craig GT, Speight PM: Expression of Mcm2, geminin and Ki67 in normal oral mucosa, oral epithelial dysplasias and their corresponding squamous-cell carcinomas. Br J Cancer; 2009 Apr 7;100(7):1128-34
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Expression of Mcm2, geminin and Ki67 in normal oral mucosa, oral epithelial dysplasias and their corresponding squamous-cell carcinomas.
  • Mcm2 and geminin have been scarcely explored in oral epithelial dysplasia (OED) and oral squamous-cell carcinoma (OSCC).
  • Mcm2 and geminin proteins seem to be novel biomarkers of growth and may be useful prognostic tools for OED.

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  • [Cites] J Cell Sci. 2004 Nov 15;117(Pt 24):5875-86 [15522891.001]
  • [Cites] Clin Cancer Res. 1999 Aug;5(8):2121-32 [10473096.001]
  • [Cites] Clin Cancer Res. 2005 Apr 1;11(7):2510-7 [15814627.001]
  • [Cites] Exp Cell Res. 2005 Sep 10;309(1):56-67 [16005865.001]
  • [Cites] Br J Cancer. 2005 Nov 28;93(11):1295-300 [16278669.001]
  • [Cites] Br J Cancer. 2006 Apr 24;94(8):1170-5 [16622441.001]
  • [Cites] Liver Int. 2006 May;26(4):424-32 [16629645.001]
  • [Cites] J Oral Pathol Med. 2006 Jul;35(6):369-75 [16762018.001]
  • [Cites] J Oral Pathol Med. 2008 Jan;37(1):1-10 [18154571.001]
  • [Cites] Proc Natl Acad Sci U S A. 2008 Jul 1;105(26):8956-61 [18579778.001]
  • [Cites] Lancet. 1999 Oct 30;354(9189):1524-5 [10551502.001]
  • [Cites] Neuropathol Appl Neurobiol. 2001 Aug;27(4):305-13 [11532161.001]
  • [Cites] Clin Cancer Res. 2001 Sep;7(9):2712-8 [11555583.001]
  • [Cites] Gut. 2002 Mar;50(3):290-1 [11839701.001]
  • [Cites] Gut. 2002 Mar;50(3):373-7 [11839717.001]
  • [Cites] Pathobiology. 2001;69(3):150-8 [11872961.001]
  • [Cites] Am J Pathol. 2002 Jul;161(1):267-73 [12107111.001]
  • [Cites] Mol Cell Biol. 2003 Apr;23(7):2351-61 [12640120.001]
  • [Cites] Head Neck. 2003 Apr;25(4):267-73 [12658730.001]
  • [Cites] J Oral Pathol Med. 2003 Sep;32(8):468-74 [12901728.001]
  • [Cites] Br J Cancer. 2003 Sep 15;89(6):1048-54 [12966424.001]
  • [Cites] Br J Cancer. 2004 Jul 19;91(2):262-9 [15199392.001]
  • [Cites] Eur J Biochem. 2004 Aug;271(16):3368-78 [15291814.001]
  • [Cites] Br J Cancer. 2004 Aug 16;91(4):714-9 [15266314.001]
  • [Cites] J Pathol. 2004 Oct;204(2):121-30 [15376260.001]
  • [Cites] J Immunol. 1984 Oct;133(4):1710-5 [6206131.001]
  • [Cites] J Cell Sci. 1994 Jan;107 ( Pt 1):253-65 [8175912.001]
  • [Cites] Cell. 1998 Jun 12;93(6):1043-53 [9635433.001]
  • [Cites] Biochim Biophys Acta. 1998 Jun 16;1398(2):113-36 [9689912.001]
  • [Cites] Proc Natl Acad Sci U S A. 1998 Dec 8;95(25):14932-7 [9843993.001]
  • [Cites] Anticancer Res. 1998 Sep-Oct;18(5B):3705-8 [9854481.001]
  • [Cites] J Pathol. 2005 Jan;205(2):123-9 [15643673.001]
  • (PMID = 19293805.001).
  • [ISSN] 1532-1827
  • [Journal-full-title] British journal of cancer
  • [ISO-abbreviation] Br. J. Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Cell Cycle Proteins; 0 / GMNN protein, human; 0 / Geminin; 0 / Ki-67 Antigen; 0 / Nuclear Proteins; EC 3.6.4.12 / MCM2 protein, human; EC 3.6.4.12 / Minichromosome Maintenance Complex Component 2
  • [Other-IDs] NLM/ PMC2669983
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94. Tsezou A, Oikonomou P, Kollia P, Mademtzis I, Kostopoulou E, Messinis I, Vamvakopoulos N: The role of human telomerase catalytic subunit mRNA expression in cervical dysplasias. Exp Biol Med (Maywood); 2005 Apr;230(4):263-70
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] The role of human telomerase catalytic subunit mRNA expression in cervical dysplasias.
  • HPV DNA was detected in all 82 specimens with abnormal cytologic findings and in 4 of 34 normal samples.
  • Low-grade squamous intraepithelial lesions (LGSILs) were present in 74 of 82 specimens (90.2%) and high-grade squamous intraepithelial lesions (HGSILs) were present in 8 of 82 (9.75%) specimens.
  • Seven of the eight HGSIL (87.5%) and 26 of 74 LGSIL (35.1%) specimens were hTERT positive, whereas all normal specimens were hTERT mRNA negative.
  • Telomerase activity was detected in 21 of 74 (28.4%) LGSIL/atypical squamous epithelial cells of undetermined significance (ASCUS) and in five of eight (62.5%) HGSIL samples.
  • [MeSH-major] Cervical Intraepithelial Neoplasia / enzymology. RNA, Messenger / analysis. Telomerase / metabolism. Uterine Cervical Dysplasia / enzymology. Uterine Cervical Neoplasms / enzymology

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  • (PMID = 15792948.001).
  • [ISSN] 1535-3702
  • [Journal-full-title] Experimental biology and medicine (Maywood, N.J.)
  • [ISO-abbreviation] Exp. Biol. Med. (Maywood)
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / DNA, Viral; 0 / DNA-Binding Proteins; 0 / RNA, Messenger; EC 2.7.7.49 / Telomerase
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95. Monte LF, Silva Filho LV, Miyoshi MH, Rozov T: [Bronchopulmonary dysplasia]. J Pediatr (Rio J); 2005 Mar-Apr;81(2):99-110
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Bronchopulmonary dysplasia].
  • [Transliterated title] Displasia broncopulmonar.
  • OBJECTIVE: To present a wide-ranging review of the literature on broncopulmonary dysplasia, covering new definitions, pathophysiology, prevention, treatment, prognosis and progression.
  • SUMMARY OF THE FINDINGS: Bronchopulmonary dysplasia is considered one of the primary causes of chronic lung disease among infants.
  • It is associated with frequent and prolonged hospital admissions, in particular for pulmonary diseases, with high rates of mortality and alterations to neuropsychomotor development and pondero-statural growth.
  • Treatment of bronchopulmonary dysplasia patients demands a multidisciplinary team.
  • CONCLUSIONS: Bronchopulmonary dysplasia has been and continues to be studied in great depth with the objective of identifying its causes and possible prevention and treatment strategies.
  • Controversies remain with respect of these issues and also about the prognosis of these patients, in particular when the subject is long-term progress of "new" bronchopulmonary dysplasia patients.
  • [MeSH-major] Bronchopulmonary Dysplasia

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  • (PMID = 15858670.001).
  • [ISSN] 0021-7557
  • [Journal-full-title] Jornal de pediatria
  • [ISO-abbreviation] J Pediatr (Rio J)
  • [Language] por
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Brazil
  • [Number-of-references] 52
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96. Merlini G, Pozzi C: Mechanisms of renal damage in plasma cell dyscrasias: an overview. Contrib Nephrol; 2007;153:66-86
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Mechanisms of renal damage in plasma cell dyscrasias: an overview.
  • The kidney is a target organ in plasma cell dyscrasias.
  • The primary structure of the monoclonal proteins is at the basis of the ultrastructural organization of their aggregates which translates into characteristic kidney injuries.
  • The kidney targeting is due to the concurrence of several factors such as the local catabolism of monoclonal LCs, specific interactions of the monoclonal proteins with tissue and cellular components, and local environmental conditions.
  • In patients with known plasma cell dyscrasia, the recognition of these patterns of renal injury should lead to appropriate therapeutic intervention.

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  • (PMID = 17075224.001).
  • [ISSN] 0302-5144
  • [Journal-full-title] Contributions to nephrology
  • [ISO-abbreviation] Contrib Nephrol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] Switzerland
  • [Chemical-registry-number] 0 / Immunoglobulin Light Chains
  • [Number-of-references] 79
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97. Masquijo JJ, Willis B: [Dysplasia epiphysealis hemimelica (Trevor's disease)]. Arch Argent Pediatr; 2010 Feb;108(1):e20-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Dysplasia epiphysealis hemimelica (Trevor's disease)].
  • [Transliterated title] Displasia epifisaria hemimélica (enfermedad de Trevor).
  • Dysplasia epiphysealis hemimelica is a rare skeletal developmental disorder characterized by asymmetric overgrowth of cartilage in the epiphyses.
  • Plain films matched with dysplasia epiphysealis hemimelica.
  • Treatment of dysplasia epiphysealis hemimelica is not clearly defined in the literature.
  • Due to the risk of recurrence, patients with this unusual dysplasia should be monitored on a regular basis.

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  • (PMID = 20204228.001).
  • [ISSN] 1668-3501
  • [Journal-full-title] Archivos argentinos de pediatría
  • [ISO-abbreviation] Arch Argent Pediatr
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Argentina
  • [Number-of-references] 15
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98. Sonneveld P, Jongen JL: Dealing with neuropathy in plasma-cell dyscrasias. Hematology Am Soc Hematol Educ Program; 2010;2010:423-30
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  • [Title] Dealing with neuropathy in plasma-cell dyscrasias.
  • Peripheral neuropathy (PN) is a frequent complication of plasma-cell dyscrasias such as monoclonal gammopathy of undetermined significance, multiple myeloma, Waldenström's disease, POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) syndrome, Castleman's disease, and light-chain amyloidosis.

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  • (PMID = 21239830.001).
  • [ISSN] 1520-4383
  • [Journal-full-title] Hematology. American Society of Hematology. Education Program
  • [ISO-abbreviation] Hematology Am Soc Hematol Educ Program
  • [Language] ENG
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
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99. Batts ED, Sanchorawala V, Hegerfeldt Y, Lazarus HM: Azotemia associated with use of lenalidomide in plasma cell dyscrasias. Leuk Lymphoma; 2008 Jun;49(6):1108-15
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  • [Title] Azotemia associated with use of lenalidomide in plasma cell dyscrasias.
  • We describe five patients with plasma cell dyscrasias and renal insufficiency (AL amyloidosis, monoclonal gammopathy of undetermined significance with Fanconi syndrome, and multiple myeloma) treated with lenalidomide and dexamethasone who developed progressive azotemia.
  • Four patients required hemodialysis after exposure to lenalidomide; two previously were untreated for their plasma cell dyscrasia.
  • We conclude that azotemia is an uncommon, but serious, potential complication of lenalidomide therapy in plasma cell dyscrasias with associated renal insufficiency.

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  • (PMID = 18452093.001).
  • [ISSN] 1029-2403
  • [Journal-full-title] Leukemia & lymphoma
  • [ISO-abbreviation] Leuk. Lymphoma
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Paraproteins; 4Z8R6ORS6L / Thalidomide; 7S5I7G3JQL / Dexamethasone; F0P408N6V4 / lenalidomide
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100. Mattioli M, Agnelli L, Fabris S, Baldini L, Morabito F, Bicciato S, Verdelli D, Intini D, Nobili L, Cro L, Pruneri G, Callea V, Stelitano C, Maiolo AT, Lombardi L, Neri A: Gene expression profiling of plasma cell dyscrasias reveals molecular patterns associated with distinct IGH translocations in multiple myeloma. Oncogene; 2005 Apr 7;24(15):2461-73
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  • [Title] Gene expression profiling of plasma cell dyscrasias reveals molecular patterns associated with distinct IGH translocations in multiple myeloma.
  • Multiple myeloma (MM) is the most common form of plasma cell dyscrasia, characterized by a marked heterogeneity of genetic lesions and clinical course.
  • To provide insights into the molecular characterization of plasma cell dyscrasias and to investigate the contribution of specific genetic lesions to the biological and clinical heterogeneity of MM, we analysed the gene expression profiles of plasma cells isolated from seven MGUS, 39 MM and six PCL patients by means of DNA microarrays.

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  • (PMID = 15735737.001).
  • [ISSN] 0950-9232
  • [Journal-full-title] Oncogene
  • [ISO-abbreviation] Oncogene
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / CCND2 protein, human; 0 / Cyclin D2; 0 / Cyclins; 0 / DNA, Neoplasm; 0 / Immunoglobulin Heavy Chains; 0 / Receptors, Interleukin-6
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