[X] Close
You are about to erase all the values you have customized, search history, page format, etc.
Click here to RESET all values       Click here to GO BACK without resetting any value
Items 1 to 100 of about 725
76. Gockel I, Kneist W, Heintz A, Beyer J, Junginger T: Endoscopic adrenalectomy: an analysis of the transperitoneal and retroperitoneal approaches and results of a prospective follow-up study. Surg Endosc; 2005 Apr;19(4):569-73
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endoscopic adrenalectomy: an analysis of the transperitoneal and retroperitoneal approaches and results of a prospective follow-up study.
  • The aim of this study was to determine which of these is the optimal surgical technique in a prospectively designed analysis of a large series of patients operated on by a single team over a 10-year period.
  • The most prevalent indication was incidentaloma (35.9%), followed by pheochromocytoma and Conn's adenoma.
  • [MeSH-minor] Adrenal Cortex Neoplasms / surgery. Adrenal Gland Neoplasms / surgery. Adrenocortical Adenoma / surgery. Adult. Aged. Body Mass Index. Cushing Syndrome / surgery. Female. Follow-Up Studies. Humans. Incidental Findings. Intraoperative Period. Male. Middle Aged. Neoplasms, Multiple Primary / surgery. Peritoneum. Pheochromocytoma / surgery. Prospective Studies. Retroperitoneal Space. Treatment Outcome

  • MedlinePlus Health Information. consumer health - Endoscopy.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Arch Surg. 2000 Aug;135(8):967-71 [10922260.001]
  • [Cites] Urology. 1997 Jul;50(1):19-24 [9218013.001]
  • [Cites] Br J Surg. 1997 May;84(5):679-82 [9171764.001]
  • [Cites] World J Surg. 2001 Jun;25(6):728-34 [11376407.001]
  • [Cites] Eur Urol. 1998;33(3):303-7 [9555557.001]
  • [Cites] J Laparoendosc Adv Surg Tech A. 2001 Dec;11(6):409-13 [11814133.001]
  • [Cites] Surgery. 1997 Dec;122(6):1132-6 [9426429.001]
  • [Cites] Ann Surg. 1997 Sep;226(3):238-46; discussion 246-7 [9339930.001]
  • [Cites] Chirurg. 1997 Feb;68(2):154-8 [9156982.001]
  • [Cites] Surg Endosc. 2000 Oct;14(10):920-5 [11080404.001]
  • [Cites] Ann Surg. 1996 Dec;224(6):727-34; discussion 734-6 [8968227.001]
  • [Cites] Am J Surg. 1999 Jul;178(1):50-3; discussion 54 [10456703.001]
  • [Cites] Ann Surg. 2000 Dec;232(6):796-803 [11088074.001]
  • [Cites] Surg Endosc. 2002 Jan;16(1):96-9 [11961614.001]
  • [Cites] Arch Surg. 1996 Aug;131(8):870-5; discussion 875-6 [8712912.001]
  • [Cites] World J Surg. 1998 Dec;22(12):1246-9 [9841752.001]
  • (PMID = 15759181.001).
  • [ISSN] 1432-2218
  • [Journal-full-title] Surgical endoscopy
  • [ISO-abbreviation] Surg Endosc
  • [Language] eng
  • [Publication-type] Evaluation Studies; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


77. Porterfield JR, Thompson GB, Young WF Jr, Chow JT, Fryrear RS, van Heerden JA, Farley DR, Atkinson JL, Meyer FB, Abboud CF, Nippoldt TB, Natt N, Erickson D, Vella A, Carpenter PC, Richards M, Carney JA, Larson D, Schleck C, Churchward M, Grant CS: Surgery for Cushing's syndrome: an historical review and recent ten-year experience. World J Surg; 2008 May;32(5):659-77
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Cushing's syndrome (CS), due to multiple etiologies, is a disorder associated with the ravages of cortisol excess.
  • The purpose of this review article is to provide a historical synopsis of surgery for CS, review a recent 10-year period of operative management at a tertiary care facility, and to outline a practical approach to diagnosis and management.
  • Fifty-four patients (18%) had cortisol-secreting adenomas, 10 patients (3%) had cortisol-producing adrenocortical carcinomas, and 1% had other causes.
  • Most benign adrenal processes could be managed laparoscopically.
  • Five-year survival rates (all causes) were 90%, 51%, and 23% for adrenocortical adenomas, ectopic ACTH syndrome, and adrenocortical carcinomas, respectively.
  • CONCLUSIONS: Surgery for CS is highly successful for pituitary-dependent CS and most ACTH-independent adrenal causes.
  • Unfortunately, to date, adrenocortical carcinomas are rarely cured.
  • Future successes with this disease will likely depend on a better understanding of tumor biology, more effective adjuvant therapies and earlier detection.

  • Genetic Alliance. consumer health - Cushing's Syndrome.
  • Genetic Alliance. consumer health - TEN.
  • MedlinePlus Health Information. consumer health - Cushing's Syndrome.
  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Arch Surg. 2001 May;136(5):543-9 [11343545.001]
  • [Cites] N Engl J Med. 1967 Nov 16;277(20):1050-6 [6059584.001]
  • [Cites] J Clin Endocrinol Metab. 1997 Jun;82(6):1776-9 [9177381.001]
  • [Cites] Medicina (B Aires). 2000;60(3):326-30 [11050809.001]
  • [Cites] J Clin Endocrinol Metab. 1998 Aug;83(8):2681-6 [9709931.001]
  • [Cites] Trends Endocrinol Metab. 2004 Oct;15(8):375-82 [15380809.001]
  • [Cites] N Engl J Med. 1991 Sep 26;325(13):897-905 [1652686.001]
  • [Cites] Neurosurg Focus. 2004 Apr 15;16(4):E5 [15191334.001]
  • [Cites] Endocrinol Metab Clin North Am. 2005 Jun;34(2):459-78, xi [15850853.001]
  • [Cites] Ann Surg. 1909 Dec;50(6):1002-17 [17862444.001]
  • [Cites] Acta Med Scand. 1980;208(1-2):101-9 [7192045.001]
  • [Cites] Endocr Relat Cancer. 2005 Sep;12(3):667-80 [16172199.001]
  • [Cites] Pituitary. 2004;7(4):209-15 [16132203.001]
  • [Cites] J Neurosurg. 2005 Sep;103(3):570-4 [16235694.001]
  • [Cites] Horm Res. 2005;64(3):140-3 [16192738.001]
  • [Cites] Clin Endocrinol (Oxf). 2001 Jun;54(6):797-804 [11422115.001]
  • [Cites] Int J Urol. 2006 Jun;13(6):677-81 [16834641.001]
  • [Cites] Arch Surg. 1998 May;133(5):541-5; discussion 545-6 [9605918.001]
  • [Cites] Radiology. 1992 Oct;185(1):143-7 [1523298.001]
  • [Cites] J Clin Endocrinol Metab. 1999 Sep;84(9):3401-2 [10487721.001]
  • [Cites] Ann Surg. 1934 Oct;100(4):670-88 [17856387.001]
  • [Cites] J Clin Endocrinol Metab. 1991 Aug;73(2):408-13 [1649842.001]
  • [Cites] J Clin Endocrinol Metab. 1995 Aug;80(8):2475-9 [7629245.001]
  • [Cites] Eur J Endocrinol. 2006 Apr;154(4):519-24 [16556713.001]
  • [Cites] Am J Surg. 1982 Sep;144(3):322-4 [7114370.001]
  • [Cites] J Clin Endocrinol Metab. 1988 May;66(5):1056-64 [3360898.001]
  • [Cites] Surg Clin North Am. 2004 Jun;84(3):875-85 [15145240.001]
  • [Cites] Acta Endocrinol (Copenh). 1990 Oct;123(4):423-30 [2173325.001]
  • [Cites] Arch Med Res. 2006 Nov;37(8):976-80 [17045113.001]
  • [Cites] World J Surg. 2004 Nov;28(11):1169-75 [15490057.001]
  • [Cites] Ann Surg. 1993 Jun;217(6):595-601; discussion 601-3 [8099474.001]
  • [Cites] Surgery. 1997 Dec;122(6):1132-6 [9426429.001]
  • [Cites] J Clin Endocrinol Metab. 2003 Dec;88(12):5593-602 [14671138.001]
  • [Cites] Cancer. 2006 Sep 15;107(6):1355-64 [16894526.001]
  • [Cites] Surgery. 2006 Dec;140(6):943-8; discussion 948-50 [17188142.001]
  • [Cites] Endocrinol Metab Clin North Am. 2005 Jun;34(2):385-402, ix-x [15850849.001]
  • [Cites] Ann Surg Oncol. 1999 Dec;6(8):719-26 [10622498.001]
  • [Cites] AJR Am J Roentgenol. 1976 Jul;127(1):23-51 [180837.001]
  • [Cites] Cancer. 2000 Feb 15;88(4):711-36 [10679640.001]
  • [Cites] Best Pract Res Clin Endocrinol Metab. 2006 Sep;20(3):483-99 [16980207.001]
  • [Cites] Surg Oncol. 2003 Aug;12(2):105-23 [12946482.001]
  • [Cites] J Endocrinol Invest. 2006 May;29(5):471-82 [16794373.001]
  • [Cites] World J Surg. 2007 Jan;31(1):65-71 [17180554.001]
  • [Cites] Endocr Rev. 2005 Oct;26(6):775-99 [15827110.001]
  • [Cites] Semin Nucl Med. 1978 Jan;8(1):23-41 [345445.001]
  • [Cites] J Clin Endocrinol Metab. 2004 Jul;89(7):3173-82 [15240590.001]
  • [Cites] J Endocrinol Invest. 2004 Jul-Aug;27(7):654-8 [15505989.001]
  • [Cites] Neurochirurgie. 2002 May;48(2-3 Pt 2):294-9 [12058134.001]
  • [Cites] Am J Rhinol. 2001 Jul-Aug;15(4):281-7 [11554662.001]
  • [Cites] J Clin Endocrinol Metab. 1999 Apr;84(4):1193-202 [10199752.001]
  • [Cites] Surg Today. 2006;36(1):94-7 [16378204.001]
  • [Cites] Surg Clin North Am. 2004 Jun;84(3):755-74 [15145233.001]
  • [Cites] Urology. 2005 Sep;66(3):476-83 [16140061.001]
  • [Cites] J Clin Endocrinol Metab. 1962 Jul;22:693-703 [14471915.001]
  • [Cites] Radiographics. 2004 Mar-Apr;24(2):435-52 [15026592.001]
  • [Cites] Ann Clin Biochem. 2000 Jan;37 ( Pt 1):85-9 [10672380.001]
  • [Cites] Ann Oncol. 2000 Oct;11(10):1281-7 [11106117.001]
  • [Cites] J Clin Endocrinol Metab. 1999 Mar;84(3):1116-21 [10084604.001]
  • [Cites] World J Surg. 1998 Jun;22(6):613-9; discussion 619-20 [9597937.001]
  • [Cites] Endocrinol Metab Clin North Am. 2005 Jun;34(2):489-99, xi [15850855.001]
  • [Cites] World J Surg. 2006 May;30(5):909-16 [16467980.001]
  • [Cites] J Clin Endocrinol Metab. 1999 Feb;84(2):487-92 [10022405.001]
  • [Cites] J Urol. 1987 Nov;138(5):1134-6 [3669155.001]
  • [Cites] Clin Endocrinol (Oxf). 1984 Dec;21(6):621-9 [6509784.001]
  • [Cites] Clin Endocrinol (Oxf). 2003 Dec;59(6):793-9 [14974924.001]
  • [Cites] Endocrinol Metab Clin North Am. 2005 Jun;34(2):293-313, viii [15850843.001]
  • [Cites] Cancer. 1998 Nov 15;83(10):2194-200 [9827725.001]
  • [Cites] Am J Med. 2005 Dec;118(12):1340-6 [16378774.001]
  • [Cites] Cancer. 2000 Mar 1;88(5):1159-65 [10699907.001]
  • [Cites] Endocrinol Metab Clin North Am. 2005 Jun;34(2):441-58, x [15850852.001]
  • [Cites] Surg Clin North Am. 2004 Jun;84(3):743-53 [15145232.001]
  • [Cites] World J Surg. 2001 Jul;25(7):934-40 [11572035.001]
  • [Cites] J Endocrinol Invest. 2000 Sep;23(8):542-4 [11021772.001]
  • [Cites] N Engl J Med. 1992 Oct 1;327(14):1033 [1387700.001]
  • [Cites] N Engl J Med. 1989 Dec 14;321(24):1659-64 [2586567.001]
  • [Cites] Surgery. 1995 Dec;118(6):1071-5; discussion 1075-6 [7491525.001]
  • [Cites] Clin Endocrinol (Oxf). 2004 Nov;61(5):553-9 [15521956.001]
  • [Cites] Lancet. 2006 May 13;367(9522):1605-17 [16698415.001]
  • [Cites] N Engl J Med. 2007 Feb 8;356(6):601-10 [17287480.001]
  • [Cites] Int J Urol. 2005 Feb;12(2):134-9 [15733106.001]
  • [Cites] Surgery. 2007 Feb;141(2):147-51; discussion 151-2 [17263968.001]
  • [Cites] Lancet. 1952 Aug 2;2(6727):226-8 [14939896.001]
  • [Cites] J Clin Endocrinol Metab. 1999 Feb;84(2):533-40 [10022412.001]
  • [Cites] N Engl J Med. 2007 Jun 7;356(23):2372-80 [17554118.001]
  • [Cites] J Neurol Neurosurg Psychiatry. 1997 May;62(5):527-8 [9153615.001]
  • [Cites] J Clin Endocrinol Metab. 2001 Dec;86(12 ):5711-4 [11739426.001]
  • [Cites] Ann Intern Med. 2003 Jun 17;138(12):980-91 [12809455.001]
  • [Cites] J Endourol. 2005 Apr;19(3):272-8 [15865511.001]
  • [Cites] AJR Am J Roentgenol. 1996 Mar;166(3):531-6 [8623622.001]
  • [Cites] J Surg Oncol. 2005 Mar 1;89(3):186-92 [15719374.001]
  • [Cites] Eur J Endocrinol. 2003 Oct;149(4):273-85 [14514341.001]
  • [Cites] J Clin Endocrinol Metab. 1989 Dec;69(6):1122-6 [2555381.001]
  • [Cites] Pituitary. 2004;7(4):265-9 [16416039.001]
  • [Cites] Am J Surg. 2005 May;189(5):581-5; discussion 585-6 [15862500.001]
  • [Cites] Microsc Res Tech. 2003 Jun 15;61(3):308-14 [12768546.001]
  • [Cites] Pituitary. 1999;1(2):125-32 [11081191.001]
  • [Cites] Endocrinol Metab Clin North Am. 2005 Jun;34(2):271-92, vii [15850842.001]
  • [Cites] JAMA. 1993 May 5;269(17):2232-8 [8386285.001]
  • [Cites] J Neurosurg. 1989 Oct;71(4):520-7 [2552045.001]
  • [Cites] Endocrinol Metab Clin North Am. 2005 Jun;34(2):403-21, x [15850850.001]
  • [Cites] Eur J Endocrinol. 2005 Apr;152(4):521-5 [15817906.001]
  • [Cites] Surgery. 1992 Dec;112(6):972-9; discussion 979-80 [1455322.001]
  • [Cites] J Clin Endocrinol Metab. 2003 Dec;88(12):5808-13 [14671173.001]
  • [Cites] Ann Surg. 1951 Sep;134(3):464-75 [14869034.001]
  • [Cites] Endocrinol Metab Clin North Am. 2005 Jun;34(2):423-39, x [15850851.001]
  • [Cites] Clin Endocrinol (Oxf). 1999 Sep;51(3):265-71 [10469003.001]
  • [Cites] AJNR Am J Neuroradiol. 2000 Apr;21(4):690-6 [10782779.001]
  • (PMID = 18196319.001).
  • [ISSN] 0364-2313
  • [Journal-full-title] World journal of surgery
  • [ISO-abbreviation] World J Surg
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 139
  •  go-up   go-down


78. Surgit O: Clipless and sutureless laparoscopic adrenalectomy carried out with the LigaSure device in 32 patients. Surg Laparosc Endosc Percutan Tech; 2010 Apr;20(2):109-13
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Laparoscopic adrenalectomy has become the standard procedure for treating patents with adrenal masses.
  • METHODS: The LigaSure device was used in 32 patients undergoing laparoscopic adrenalectomy for adrenal masses.
  • In 1 patient the adrenal tumor had invaded the ipsilateral kidney, so laparoscopic nephrectomy was also carried out during the same operation.
  • In another patient, a renal cell carcinoma in the left kidney had metastasized to the right adrenal gland.
  • Both the kidney and the contralateral adrenal gland were removed laparoscopically during the same operation.
  • RESULTS: Adrenal masses had a mean greatest diameter of 3.48 cm (range 2 to 11 cm).
  • Adrenal tumor types included adrenocortical adenoma (16 patients), pheochromocytoma (13 patients), malignant pheochromocytoma (1 patient), chromophobic carcinoma (1 patient), and metastasis from a renal cell carcinoma (1 patient).
  • For patients with conditions such as renal cell carcinoma combined with metastasis to the contralateral adrenal gland, nephrectomy, and contralateral adrenalectomy can be carried out during the same laparoscopic operation.
  • [MeSH-minor] Adenoma, Chromophobe / surgery. Adrenal Gland Neoplasms / secondary. Adrenal Gland Neoplasms / surgery. Adrenocortical Adenoma / surgery. Adult. Aged. Blood Loss, Surgical. Carcinoma, Renal Cell / secondary. Carcinoma, Renal Cell / surgery. Female. Humans. Kidney Neoplasms / surgery. Male. Middle Aged. Nephrectomy / methods. Pheochromocytoma / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20393338.001).
  • [ISSN] 1534-4908
  • [Journal-full-title] Surgical laparoscopy, endoscopy & percutaneous techniques
  • [ISO-abbreviation] Surg Laparosc Endosc Percutan Tech
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


79. Eldahshan S, Celia A, Zeccolini G, Guerini A, Breda G: Laparoscopic transperitoneal adrenalectomy for adrenocortical oncocytoma. Arch Ital Urol Androl; 2008 Jun;80(2):82-4
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Laparoscopic transperitoneal adrenalectomy for adrenocortical oncocytoma.
  • A middle aged male patient (39 year old) presented with right renal pain.
  • During evaluation a small renal stone was found in the right kidney, and a mass 6 cm in diameter related to the upper pole of the left kidney was discovered.
  • Final pathology was adrenocortical oncocytoma with malignant potential.

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18683814.001).
  • [ISSN] 1124-3562
  • [Journal-full-title] Archivio italiano di urologia, andrologia : organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica
  • [ISO-abbreviation] Arch Ital Urol Androl
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
  •  go-up   go-down


80. Perretta S, Campagnacci R, Guerrieri M, Paganini AM, De Sanctis A, Sarnari J, Rimini M, Lezoche E: Sub-mesocolic access in laparoscopic left adrenalectomy. Surg Endosc; 2005 Jul;19(7):977-80
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: This article reports an alternative laparoscopic access to left adrenal gland.
  • Indications were Conn adenoma (55 cases), incidentaloma (64), Cushing adenoma (45), pheochromocytoma (32), adreno-genital syndrome (two), mielolipoma (two), and metastatic mass(nine).
  • Of 209, in 12 cases the left adrenalectomy was performed through a submesocolic access (seven pheochromocytoma, two incidentaloma, two Cushing adenoma, one Conn adenoma,).
  • The identification and closure of the adrenal vein with minimal gland manipulation resulted the main benefit of this approach.
  • CONCLUSIONS: Left adrenal lesions, as selected cases of pheochromocytoma, can be safely treated by laparoscopic submesocolic access.
  • [MeSH-major] Adrenal Cortex Neoplasms / surgery. Adrenal Gland Neoplasms / surgery. Adrenalectomy / methods. Laparoscopy
  • [MeSH-minor] Adrenocortical Adenoma / surgery. Adult. Aged. Female. Humans. Male. Middle Aged. Pheochromocytoma / surgery. Surgical Instruments

  • MedlinePlus Health Information. consumer health - Adrenal Gland Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Surg Clin North Am. 1996 Jun;76(3):523-37 [8669012.001]
  • [Cites] Surgery. 1996 Oct;120(4):706-9; discussion 710-1 [8862381.001]
  • [Cites] World J Surg. 1999 Apr;23(4):389-96 [10030863.001]
  • [Cites] Surg Endosc. 1996 Oct;10(10):987-90 [8864091.001]
  • [Cites] Urology. 1997 May;49(5):673-8 [9145969.001]
  • [Cites] Am J Surg. 1997 Feb;173(2):120-5 [9074377.001]
  • [Cites] World J Surg. 1998 Dec;22(12):1250-5 [9841753.001]
  • [Cites] Br J Surg. 1997 May;84(5):679-82 [9171764.001]
  • [Cites] Am J Surg. 1998 Jun;175(6):488-90 [9645778.001]
  • [Cites] Nihon Hinyokika Gakkai Zasshi. 1992 Jul;83(7):1130-3 [1387181.001]
  • [Cites] Eur Urol. 2004 Feb;45(2):226-32 [14734011.001]
  • [Cites] Surg Endosc. 2002 Jan;16(1):100-2 [11961615.001]
  • [Cites] ANZ J Surg. 2004 Jun;74(6):429-33 [15191473.001]
  • [Cites] Surg Endosc. 1996 Sep;10(9):912-5 [8703150.001]
  • [Cites] Surg Endosc. 2002 Feb;16(2):258-62 [11967674.001]
  • [Cites] J Am Coll Surg. 1996 Jul;183(1):1-10 [8673301.001]
  • [Cites] J Urol. 1995 Nov;154(5):1652-4 [7563312.001]
  • [Cites] N Engl J Med. 1992 Oct 1;327(14):1033 [1387700.001]
  • [Cites] J Urol. 2001 Aug;166(2):429-36 [11458042.001]
  • [Cites] Surg Endosc. 2002 Jan;16(1):96-9 [11961614.001]
  • [Cites] Eur J Endocrinol. 1998 May;138(5):548-53 [9625367.001]
  • [Cites] Surg Laparosc Endosc. 1997 Aug;7(4):275-80 [9282754.001]
  • [Cites] J Urol. 2001 Aug;166(2):437-43 [11458043.001]
  • [Cites] Ann Surg. 1997 May;225(5):495-501; discussion 501-2 [9193177.001]
  • [Cites] Eur J Surg. 1999 Aug;165(8):767-71 [10494643.001]
  • [Cites] Surg Endosc. 2004 Apr;18(4):621-5 [15026894.001]
  • [Cites] Surg Endosc. 2001 Feb;15(2):220 [11285972.001]
  • (PMID = 15920687.001).
  • [ISSN] 1432-2218
  • [Journal-full-title] Surgical endoscopy
  • [ISO-abbreviation] Surg Endosc
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


81. Terui K, Sakihara S, Kageyama K, Nigawara T, Takayasu S, Matsuhashi Y, Kon A, Yamamoto H, Ohyama C, Sasano H, Suda T: A case of adrenocortical oncocytoma occurring with aldosteronoma. J Clin Endocrinol Metab; 2010 Aug;95(8):3597-8
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A case of adrenocortical oncocytoma occurring with aldosteronoma.
  • [MeSH-major] Adenoma, Oxyphilic / pathology. Adrenal Cortex Neoplasms / pathology. Adrenocortical Adenoma / pathology. Neoplasms, Multiple Primary / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20685888.001).
  • [ISSN] 1945-7197
  • [Journal-full-title] The Journal of clinical endocrinology and metabolism
  • [ISO-abbreviation] J. Clin. Endocrinol. Metab.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


82. Giordano TJ: Molecular pathology of adrenal cortical tumors: separating adenomas from carcinomas. Endocr Pathol; 2006;17(4):355-63
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Molecular pathology of adrenal cortical tumors: separating adenomas from carcinomas.
  • Adrenal cortical carcinoma is a rare but interesting endocrine tumor.
  • Its diagnosis is usually straightforward using morphologic assessment and supplemental immunohistochemistry.
  • Here, the relevant molecular pathology of adrenal cortical tumors is reviewed with special reference to those methods (e.g., DNA microarrays) that hold promise for improved diagnosis and prognosis, and prediction of therapeutic response.
  • [MeSH-major] Adrenal Cortex Neoplasms / pathology. Adrenocortical Adenoma / pathology. Adrenocortical Carcinoma / pathology
  • [MeSH-minor] Biomarkers, Tumor / genetics. Biomarkers, Tumor / metabolism. DNA, Neoplasm / analysis. Diagnosis, Differential. Humans. Immunohistochemistry. Oligonucleotide Array Sequence Analysis. Principal Component Analysis

  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] J Clin Endocrinol Metab. 2001 Oct;86(10):4970-3 [11600572.001]
  • [Cites] Cancer Res. 2003 Oct 15;63(20):6643-50 [14583457.001]
  • [Cites] J Clin Endocrinol Metab. 1995 Feb;80(2):492-6 [7531713.001]
  • [Cites] Mod Pathol. 1998 Dec;11(12):1165-70 [9872646.001]
  • [Cites] J Clin Endocrinol Metab. 2005 Mar;90(3):1819-29 [15613424.001]
  • [Cites] J Clin Endocrinol Metab. 1994 Mar;78(3):790-4 [8126158.001]
  • [Cites] Endocr Pathol. 2001 Winter;12(4):429-35 [11949624.001]
  • [Cites] Cancer Res. 2003 Sep 1;63(17):5308-19 [14500362.001]
  • [Cites] J Natl Cancer Inst. 1992 May 6;84(9):703-7 [1569604.001]
  • [Cites] Cancer Res. 2005 Sep 1;65(17):7622-7 [16140927.001]
  • [Cites] Endocr Relat Cancer. 2005 Sep;12(3):667-80 [16172199.001]
  • [Cites] Mol Pathol. 2000 Dec;53(6):289-94 [11193046.001]
  • [Cites] Int J Cancer. 1993 May 28;54(3):408-10 [8509216.001]
  • [Cites] Eur J Endocrinol. 2001 Aug;145(2):207-12 [11454518.001]
  • [Cites] J Clin Endocrinol Metab. 2002 Sep;87(9):4324-9 [12213893.001]
  • [Cites] Eur J Clin Invest. 2000 Dec;30 Suppl 3:69-75 [11281373.001]
  • [Cites] Endocr Pathol. 1997 Spring;8(1):29-36 [12114669.001]
  • [Cites] Endocr Pathol. 2005 Fall;16(3):163-72 [16299399.001]
  • [Cites] Endocr Relat Cancer. 2004 Jun;11(2):265-80 [15163302.001]
  • [Cites] Genes Chromosomes Cancer. 2002 May;34(1):48-57 [11921282.001]
  • [Cites] Exp Clin Endocrinol Diabetes. 2005 May;113(5):248-51 [15926108.001]
  • [Cites] J Clin Endocrinol Metab. 2002 Mar;87(3):1170-6 [11889182.001]
  • [Cites] Genes Chromosomes Cancer. 2000 Jun;28(2):145-52 [10824999.001]
  • [Cites] Eur J Endocrinol. 2005 Oct;153(4):477-87 [16189167.001]
  • [Cites] Endocr Pathol. 2003 Summer;14(2):107-16 [12858000.001]
  • [Cites] Eur J Radiol. 2002 Feb;41(2):88-94 [11809538.001]
  • [Cites] J Clin Endocrinol Metab. 1997 Aug;82(8):2559-65 [9253334.001]
  • [Cites] Nat Rev Cancer. 2001 Nov;1(2):151-7 [11905806.001]
  • [Cites] Cancer Res. 2001 Sep 15;61(18):6762-7 [11559548.001]
  • [Cites] J Endocrinol Invest. 2006 Apr;29(4):298-302 [16699294.001]
  • [Cites] J Clin Endocrinol Metab. 1994 Jun;78(6):1444-53 [7911125.001]
  • [Cites] Am J Pathol. 2003 Feb;162(2):521-31 [12547710.001]
  • [Cites] Am J Hum Genet. 1999 Oct;65(4):995-1006 [10486318.001]
  • [Cites] Mod Pathol. 1997 Sep;10(9):901-7 [9310953.001]
  • [Cites] J Clin Endocrinol Metab. 1996 Oct;81(10):3636-8 [8855814.001]
  • [Cites] Eur J Surg Oncol. 2005 Jun;31(5):549-54 [15922892.001]
  • [Cites] Hum Genet. 1999 Dec;105(6):603-10 [10647896.001]
  • [Cites] J Clin Endocrinol Metab. 2005 May;90(5):2976-81 [15741269.001]
  • [Cites] Horm Metab Res. 2005 Apr;37(4):231-5 [15952083.001]
  • [Cites] Urology. 2001 Jan;57(1):176-82 [11164177.001]
  • [Cites] Endocr J. 2000 Aug;47(4):461-6 [11075727.001]
  • [Cites] J Pathol. 2001 Sep;195(1):41-52 [11568890.001]
  • [Cites] Cancer Res. 1996 Sep 15;56(18):4219-23 [8797595.001]
  • [Cites] J Clin Endocrinol Metab. 2000 Jan;85(1):441-8 [10634422.001]
  • [Cites] J Clin Endocrinol Metab. 1998 May;83(5):1713-20 [9589681.001]
  • [Cites] Arq Bras Endocrinol Metabol. 2004 Oct;48(5):647-50 [15761534.001]
  • [Cites] Nat Rev Neurosci. 2004 Oct;5(10):782-92 [15378038.001]
  • [Cites] Endocr Pathol. 2005 Summer;16(2):99-105 [16199894.001]
  • [Cites] J Clin Endocrinol Metab. 2006 Jan;91(1):14-21 [16234301.001]
  • [Cites] J Clin Invest. 2005 Jan;115(1):94-101 [15630448.001]
  • [Cites] J Clin Endocrinol Metab. 1997 Jun;82(6):1766-71 [9177379.001]
  • [Cites] J Clin Endocrinol Metab. 2002 Jul;87(7):3467-74 [12107267.001]
  • [Cites] J Clin Endocrinol Metab. 1999 Jan;84(1):216-9 [9920087.001]
  • [Cites] Horm Metab Res. 2004 Jun;36(6):397-405 [15241731.001]
  • [Cites] Trends Endocrinol Metab. 2003 Nov;14(9):404-10 [14580759.001]
  • [Cites] J Natl Cancer Inst. 1994 Nov 16;86(22):1707-10 [7966399.001]
  • [Cites] J Clin Endocrinol Metab. 1993 Sep;77(3):852-8 [8370710.001]
  • [Cites] J Mol Endocrinol. 1999 Aug;23(1):23-32 [10425444.001]
  • [Cites] J Clin Endocrinol Metab. 1994 Feb;78(2):483-91 [8106638.001]
  • (PMID = 17525484.001).
  • [ISSN] 1046-3976
  • [Journal-full-title] Endocrine pathology
  • [ISO-abbreviation] Endocr. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / DNA, Neoplasm
  • [Number-of-references] 59
  •  go-up   go-down


83. Inan N, Arslan A, Akansel G, Anik Y, Balci NC, Demirci A: Dynamic contrast enhanced MRI in the differential diagnosis of adrenal adenomas and malignant adrenal masses. Eur J Radiol; 2008 Jan;65(1):154-62
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Dynamic contrast enhanced MRI in the differential diagnosis of adrenal adenomas and malignant adrenal masses.
  • OBJECTIVE: To evaluate the value of dynamic MR imaging in the differential diagnosis of adrenal adenomas and malignant tumors, especially in cases with atypical adenomas.
  • MATERIALS AND METHODS: Sixty-four masses (48 adenomas, 16 malignant tumors) were included in this prospective study.
  • RESULTS: Chemical shift MR imaging was able to differentiate 44 out of 48 adenomas (91.7%) from non-adenomas.
  • The 4 adenomas (8.3%) which could not be differentiated from non-adenomas by this technique did not exhibit signal loss on out-of-phase images.
  • With a cut-off value of 30, SI indices of adenomas had a sensitivity of 93.8%, specificity of 100% and a positive predictive value of 100%.
  • On visual evaluation of dynamic MR imaging, early phase contrast enhancement patterns were homogeneous in 75% and punctate in 20,83% of the adenomas; while patchy in 56.25% and peripheral in 25% of the malignant tumors.
  • On the late phase images 58.33% of the adenomas showed peripheral ring-shaped enhancement and 10.41% showed heterogeneous enhancement.
  • At the 25th second, the SIs and wash-in rates of the adenomas were significantly higher than those of the malignant masses (p=0.010).
  • Time-to-peak enhancement of the malignant masses was significantly longer than that of the adenomas.
  • CONCLUSION: Chemical shift MR has a high sensitivity and specificity in the differential diagnosis of adenomas and malignant adrenal masses.
  • However, taking into consideration only the atypical adenomas, chemical shift MRI is of no diagnostic value.
  • [MeSH-major] Adrenal Gland Neoplasms / diagnosis. Adrenocortical Adenoma / diagnosis. Magnetic Resonance Imaging / methods
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Contrast Media. Diagnosis, Differential. Female. Humans. Image Interpretation, Computer-Assisted. Male. Middle Aged. ROC Curve. Sensitivity and Specificity. Statistics, Nonparametric

  • MedlinePlus Health Information. consumer health - Adrenal Gland Cancer.
  • MedlinePlus Health Information. consumer health - MRI Scans.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17466481.001).
  • [ISSN] 0720-048X
  • [Journal-full-title] European journal of radiology
  • [ISO-abbreviation] Eur J Radiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Ireland
  • [Chemical-registry-number] 0 / Contrast Media
  •  go-up   go-down


8
Advertisement
4. Pai SG, Shivashankara KN, Pandit V, Sheshadri S: Symptomatic hypocalcemia in primary hyperaldosteronism: a case report. J Korean Med Sci; 2009 Dec;24(6):1220-3
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • But its effects on calcium metabolism, parathyroid metabolism and renal handling of calcium are less well described.
  • We hereby report a case of primary hyperaldosteronism due to adrenal adenoma (Conn's syndrome) who presented with a myriad of clinical features including symptomatic hypocalcemia, significant weight loss along with uncontrolled hypertension for a prolonged period before eventually detected to have primary hyperaldosteronism.
  • [MeSH-major] Adrenal Cortex Neoplasms / complications. Adrenocortical Adenoma / complications. Hyperaldosteronism. Hypocalcemia / etiology

  • Genetic Alliance. consumer health - Hyperaldosteronism.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Am J Physiol Heart Circ Physiol. 2004 Nov;287(5):H2023-6 [15475529.001]
  • [Cites] Kidney Int. 1972 Nov;2(5):279-86 [4670906.001]
  • [Cites] J Natl Med Assoc. 1993 Oct;85(10):761-3 [8254693.001]
  • [Cites] Dtsch Med Wochenschr. 1993 Dec 17;118(50):1837-43 [8269828.001]
  • [Cites] Am J Hypertens. 1995 Sep;8(9):884-93 [8541003.001]
  • [Cites] N Engl J Med. 2001 Dec 6;345(23):1689-97 [11759649.001]
  • [Cites] J Lab Clin Med. 1955 Jan;45(1):3-17 [13233623.001]
  • [Cites] Circulation. 2005 Feb 22;111(7):871-8 [15710759.001]
  • [Cites] Am J Physiol Heart Circ Physiol. 2006 Jan;290(1):H286-94 [16373592.001]
  • [Cites] J Postgrad Med. 1995 Jan-Mar;41(1):17-8 [10740696.001]
  • [Cites] Endocr J. 1995 Aug;42(4):481-7 [8556054.001]
  • (PMID = 19949688.001).
  • [ISSN] 1598-6357
  • [Journal-full-title] Journal of Korean medical science
  • [ISO-abbreviation] J. Korean Med. Sci.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2775880
  • [Keywords] NOTNLM ; Hypocalcemia / Primary Aldosteronism / Weight Loss
  •  go-up   go-down


85. Browning L, Bailey D, Parker A: D2-40 is a sensitive and specific marker in differentiating primary adrenal cortical tumours from both metastatic clear cell renal cell carcinoma and phaeochromocytoma. J Clin Pathol; 2008 Mar;61(3):293-6
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] D2-40 is a sensitive and specific marker in differentiating primary adrenal cortical tumours from both metastatic clear cell renal cell carcinoma and phaeochromocytoma.
  • BACKGROUND: The morphological similarities between the cells of clear cell renal cell carcinoma (CCRCC) and those of the adrenal cortex impose diagnostic difficulties, for example in the context of a solitary nodule in the adrenal gland in a patient with renal cell carcinoma (RCC).
  • D2-40, an antibody commonly used to highlight lymphatic endothelial cells, is consistently positive in the normal adrenal cortex.
  • AIMS: To investigate the utility of D2-40 in distinguishing neoplastic and non-neoplastic adrenal cortical cells from those of CCRCC, and from phaeochromocytoma.
  • METHODS: D2-40 antibody was applied to tissue sections from 10 normal adrenal glands, 15 renal carcinomas (13 clear cell, 2 papillary variants), 1 metastatic CCRCC in the adrenal gland, 6 adrenal cortical hyperplasias, 5 adrenal cortical adenomas, 3 adrenal cortical carcinomas, and 4 phaeochromocytomas.
  • RESULTS: D2-40 was strongly and diffusely positive in the cells of the neoplastic and non-neoplastic adrenal cortex, but negative in the cells of the CCRCC, both primary and metastatic, in 100% of the cases.
  • The cells of the adrenal medulla, and those of the phaeochromocytomas, were negative for D2-40.
  • CONCLUSIONS: D2-40 may be a useful marker for distinguishing primary adrenal cortical neoplasms from both metastatic CCRCC and phaeochromocytoma.
  • [MeSH-major] Adrenal Cortex Neoplasms / diagnosis. Antibodies, Monoclonal / analysis. Biomarkers, Tumor / analysis. Carcinoma, Renal Cell / secondary. Kidney Neoplasms / secondary. Pheochromocytoma / diagnosis
  • [MeSH-minor] Adenoma / diagnosis. Adrenal Glands / immunology. Antibodies, Monoclonal, Murine-Derived. Carcinoma / diagnosis. Cytoplasm / immunology. Diagnosis, Differential. Humans. Immunohistochemistry


86. Vascik T: Case of the month. JAAPA; 2009 Dec;22(12):70
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Adrenal Cortex Neoplasms / diagnosis. Adrenocortical Adenoma / diagnosis
  • [MeSH-minor] Adrenalectomy. Adult. Diagnosis, Differential. Humans. Hypertension / etiology. Hypokalemia / etiology. Male

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 24887476.001).
  • [ISSN] 1547-1896
  • [Journal-full-title] JAAPA : official journal of the American Academy of Physician Assistants
  • [ISO-abbreviation] JAAPA
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


87. Schön G: [Laparoscopic adrenalectomy]. Aktuelle Urol; 2010 Sep;41(5):329-38; quiz 339-40
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Adrenal Gland Neoplasms / surgery. Adrenalectomy / methods. Laparoscopy / methods. Neuroendocrine Tumors / surgery
  • [MeSH-minor] Adrenal Cortex Neoplasms / diagnosis. Adrenal Cortex Neoplasms / surgery. Adrenocortical Adenoma / diagnosis. Adrenocortical Adenoma / surgery. Cushing Syndrome / diagnosis. Cushing Syndrome / surgery. Diagnosis, Differential. Diagnostic Imaging. Hormones / blood. Humans

  • MedlinePlus Health Information. consumer health - Adrenal Gland Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20824578.001).
  • [ISSN] 1438-8820
  • [Journal-full-title] Aktuelle Urologie
  • [ISO-abbreviation] Aktuelle Urol
  • [Language] ger
  • [Publication-type] Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Hormones
  •  go-up   go-down


88. Dluhy RG: Incidentaloma--role of the endocrinologist. Endocr Pract; 2008 Apr;14(3):267-8
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Adrenal Cortex Neoplasms / radiography. Adrenocortical Adenoma / radiography. Incidental Findings

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [CommentOn] Endocr Pract. 2008 Apr;14(3):279-84 [18463033.001]
  • [CommentOn] Endocr Pract. 2008 Apr;14(3):269-78 [18463032.001]
  • (PMID = 18463031.001).
  • [ISSN] 1934-2403
  • [Journal-full-title] Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
  • [ISO-abbreviation] Endocr Pract
  • [Language] eng
  • [Publication-type] Comment; Editorial
  • [Publication-country] United States
  •  go-up   go-down


89. Adler JT, Mack E, Chen H: Isolated adrenal mass in patients with a history of cancer: remember pheochromocytoma. Ann Surg Oncol; 2007 Aug;14(8):2358-62
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Isolated adrenal mass in patients with a history of cancer: remember pheochromocytoma.
  • BACKGROUND: In a patient with a history of cancer, an isolated adrenal mass is usually thought to be a metastasis.
  • This study was undertaken to determine the incidence of functional adrenal lesions in patients with a history of cancer and examine predictive factors for the type of lesion.
  • METHODS: At a single institution, 33 patients with an isolated adrenal mass and a history of cancer underwent surgical treatment.
  • Patients' records were retrospectively analyzed for type of adrenal lesion and other diagnostic parameters.
  • Of these, 20 (61%) had adrenal metastases, 8 (24%) had pheochromocytomas, and 5 (15%) had adrenal adenomas.
  • CONCLUSIONS: Nearly 1 in 4 resected adrenal masses in patients with a history of cancer were pheochromocytomas.
  • Therefore, remember one thing in patients with an isolated adrenal mass and a history of cancer: pheochromocytoma.
  • [MeSH-major] Adrenal Gland Neoplasms. Medical Records. Pheochromocytoma
  • [MeSH-minor] Adenoma / pathology. Adrenalectomy. Analysis of Variance. Female. Humans. Incidence. Male. Middle Aged. Neoplasm Metastasis. Neoplasms / pathology. Positron-Emission Tomography. Retrospective Studies. Tumor Burden


90. Halefoglu AM, Bas N, Yasar A, Basak M: Differentiation of adrenal adenomas from nonadenomas using CT histogram analysis method: a prospective study. Eur J Radiol; 2010 Mar;73(3):643-51
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Differentiation of adrenal adenomas from nonadenomas using CT histogram analysis method: a prospective study.
  • OBJECTIVE: The objective of our study was to prospectively evaluate the effectiveness of computed tomography (CT) histogram analysis method in the differentiation of benign and malignant adrenal masses.
  • MATERIALS AND METHODS: Between March 2007 and June 2008, 94 patients (46 males, 48 females, age range: 30-79 years, mean age: 57.7 years) with 113 adrenal masses (mean diameter: 3.03 cm, range: 1.07-8.02 cm) were prospectively evaluated.
  • These included 66 adenomas, 45 metastases and 2 pheochromocytomas.
  • Histogram analysis method was performed using a circular region of interest (ROI) and mean attenuation, total number of pixels, number of negative pixels and subsequent percentage of negative pixels were detected on both unenhanced and delayed contrast-enhanced CT images for each adrenal mass.
  • Final diagnoses were based on imaging follow-up of minimum 6 months, biopsy, surgery and adrenal washout study.
  • RESULTS: 51 of 66 adenomas (77.3%) showed attenuation values of < or =10HU and 15 (22.7%) adenomas showed more than 10HU on unenhanced CT.
  • All of these adenomas contained negative pixels on unenhanced CT.
  • Eight of 66 (12.1%) adenomas showed a mean attenuation value of < or =10HU on delayed contrast-enhanced scans and 45 adenomas (68.2%) persisted on containing negative pixels.
  • Both methods gave a 100% specificity for the diagnosis of adenoma.
  • CONCLUSION: The CT histogram analysis is a simple and easily applicable method which provides higher sensitivity than the commonly used 10HU threshold mean attenuation method of unenhanced CT and can replace it for the diagnosis of an adenoma.
  • But with contrast-enhanced CT, although 100% specificity is being maintained, the sensitivities obtained are very poor for each method and is therefore likely to limit CT histogram analysis to be used as a clinically useful adjunct in the diagnosis of adenoma.
  • [MeSH-major] Adrenal Gland Neoplasms / radiography. Adrenocortical Adenoma / radiography. Pheochromocytoma / radiography. Tomography, Spiral Computed / methods
  • [MeSH-minor] Adult. Aged. Contrast Media. Diagnosis, Differential. Female. Humans. Iohexol / analogs & derivatives. Male. Middle Aged. Prospective Studies. Sensitivity and Specificity

  • MedlinePlus Health Information. consumer health - Adrenal Gland Cancer.
  • MedlinePlus Health Information. consumer health - Pheochromocytoma.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Copyright] Copyright 2008 Elsevier Ireland Ltd. All rights reserved.
  • (PMID = 19167179.001).
  • [ISSN] 1872-7727
  • [Journal-full-title] European journal of radiology
  • [ISO-abbreviation] Eur J Radiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Ireland
  • [Chemical-registry-number] 0 / Contrast Media; 4419T9MX03 / Iohexol; 712BAC33MZ / iopromide
  •  go-up   go-down


91. Tritos NA: Diagnosis of primary aldosteronism in a patient with an incidentally found adrenal mass. Nat Clin Pract Endocrinol Metab; 2007 Jul;3(7):547-51
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Diagnosis of primary aldosteronism in a patient with an incidentally found adrenal mass.
  • BACKGROUND: A 50-year-old woman who was complaining of abdominal pain was referred to the endocrine clinic after a small (0.8 cm by 0.8 cm) mass was found in her right adrenal gland on CT examination of the abdomen.
  • She had a history of hypertension for 10 years, generalized anxiety disorder for 5 years and a weight increase of 18 kg over the previous 3 years.
  • In addition, measurements of urine aldosterone excretion on a high-salt diet, MRI-examination of the adrenal glands and bilateral adrenal vein sampling were conducted.
  • DIAGNOSIS: An aldosterone-secreting adrenal adenoma.
  • MANAGEMENT: The patient underwent laparoscopic resection of the right adrenal gland, which led to normalization of aldosterone excretion, lowering of her blood pressure on a single antihypertensive medication (50 mg sustained-release metoprolol daily) and resolution of hypokalemia.
  • [MeSH-major] Adenoma / diagnosis. Adrenal Gland Neoplasms / diagnosis. Adrenal Glands / pathology. Hyperaldosteronism / diagnosis
  • [MeSH-minor] Adrenalectomy. Aldosterone / blood. Diagnosis, Differential. Female. Humans. Magnetic Resonance Imaging. Middle Aged

  • Genetic Alliance. consumer health - Primary aldosteronism.
  • MedlinePlus Health Information. consumer health - Adrenal Gland Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17581624.001).
  • [ISSN] 1745-8374
  • [Journal-full-title] Nature clinical practice. Endocrinology & metabolism
  • [ISO-abbreviation] Nat Clin Pract Endocrinol Metab
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 4964P6T9RB / Aldosterone
  •  go-up   go-down


92. El-Kappany HA, Shoma AM, El-Tabey NA, El-Nahas AR, Eraky II: Laparoscopic adrenalectomy: a single-center experience of 43 cases. J Endourol; 2005 Dec;19(10):1170-3
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Functioning adrenal masses and solid masses>5 cm were the most common indications.
  • Intraoperative complications occurred in 3 cases (6.9%), necessitating conversion to open surgery in 2 to control bleeding from the avulsed right adrenal vein.
  • A third case of conversion was elective because of difficult dissection of a large left pheochromocytoma from the renal hilum, so there was a 6.9% rate of conversion to open surgery.
  • CONCLUSION: Laparoscopic adrenalectomy is surgically feasible and can be applied for different adrenal pathologies.

  • MedlinePlus Health Information. consumer health - Adrenal Gland Cancer.
  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16359207.001).
  • [ISSN] 0892-7790
  • [Journal-full-title] Journal of endourology
  • [ISO-abbreviation] J. Endourol.
  • [Language] ENG
  • [Publication-type] Evaluation Studies; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


93. Rossbach HC, Baschinsky D, Wynn T, Obzut D, Sutcliffe M, Tebbi C: Composite adrenal anaplastic neuroblastoma and virilizing adrenocortical tumor with germline TP53 R248W mutation. Pediatr Blood Cancer; 2008 Mar;50(3):681-3
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Composite adrenal anaplastic neuroblastoma and virilizing adrenocortical tumor with germline TP53 R248W mutation.
  • Such tumors in adrenal glands are usually of neuroendocrine-neural type and occur mostly in adults.
  • We report a patient with composite neuroblastoma (NB), adrenocortical tumor (ACT), and Li-Fraumeni syndrome (LFS) with germline TP53 R248W mutation.
  • LFS predisposes to the development of leukemia, sarcomas, adrenocortical and breast carcinomas, brain tumors and, questionably, NB.
  • [MeSH-major] Adrenal Cortex Neoplasms / pathology. Adrenal Gland Neoplasms / pathology. Adrenocortical Adenoma / pathology. Genes, p53. Germ-Line Mutation. Li-Fraumeni Syndrome / genetics. Mutation, Missense. Neoplasms, Multiple Primary / pathology. Neuroblastoma / pathology. Point Mutation. Virilism / etiology


94. Sahdev A, Reznek RH, Evanson J, Grossman AB: Imaging in Cushing's syndrome. Arq Bras Endocrinol Metabol; 2007 Nov;51(8):1319-28
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Once the diagnosis of Cushing's syndrome (CS) has been established, the main step is to differentiate between ACTH dependent and independent disease.
  • In adults, 80% of CS is due to ACTH-dependent causes and 20% due to adrenal causes.
  • These are usually anterior pituitary microadenomas, which result in the classic Cushing's disease.
  • Non-pituitary ectopic sources of ACTH, such as a small-cell lung carcinoma or carcinoid tumours, are the source of the remainder of ACTH-dependent disease.
  • Imaging is essential for determining the source of ACTH in ectopic ACTH production, locating the pituitary tumours and distinguishing adrenal adenomas, carcinomas and hyperplasias.
  • In our chapter we review the adrenal appearances in ACTH-dependent and ACTH-independent CS.
  • We also include a discussion on the use of MRI and CT for the detection and management of pituitary ACTH secreting adenomas.
  • CT of the chest, abdomen and pelvis with intravenous injection of contrast medium is the most sensitive imaging modality for the identification of the ectopic ACTH source and detecting adrenal pathology.
  • MRI is used for characterising adrenal adenomas, problem solving in difficult cases and for detecting ACTH-secreting pituitary adenomas.
  • [MeSH-major] ACTH-Secreting Pituitary Adenoma / diagnosis. Cushing Syndrome / diagnosis. Pituitary Gland / pathology. Pituitary Neoplasms / diagnosis
  • [MeSH-minor] ACTH Syndrome, Ectopic / diagnosis. Adenoma / diagnosis. Adenoma / radiography. Adrenal Gland Neoplasms / diagnosis. Adrenal Gland Neoplasms / radiography. Carcinoma / diagnosis. Carcinoma / radiography. Humans. Hyperplasia / diagnosis. Hyperplasia / radiography. Lung Neoplasms / diagnosis. Lung Neoplasms / secretion. Magnetic Resonance Imaging. Tomography, X-Ray Computed

  • Genetic Alliance. consumer health - Cushing's Syndrome.
  • MedlinePlus Health Information. consumer health - Cushing's Syndrome.
  • MedlinePlus Health Information. consumer health - Pituitary Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18209870.001).
  • [ISSN] 0004-2730
  • [Journal-full-title] Arquivos brasileiros de endocrinologia e metabologia
  • [ISO-abbreviation] Arq Bras Endocrinol Metabol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] Brazil
  • [Number-of-references] 36
  •  go-up   go-down


95. Tamura Y, Adachi J, Chiba Y, Mori S, Takeda K, Kasuya Y, Murayama T, Sawabe M, Sasano H, Araki A, Ito H, Horiuchi T: Primary aldosteronism due to unilateral adrenal microadenoma in an elderly patient: efficacy of selective adrenal venous sampling. Intern Med; 2008;47(1):37-42
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary aldosteronism due to unilateral adrenal microadenoma in an elderly patient: efficacy of selective adrenal venous sampling.
  • Computed tomography imaging appeared normal for a long duration with a left-sided nodule appearing far later; adrenal scintigraphy was first normal, and the second test showed right-sided uptake.
  • However, a repeat selective adrenal venous sampling (SAVS) indicated a left-sided lateralization of the hypersecretion of aldosterone.
  • [MeSH-major] Adrenal Cortex Neoplasms / blood. Adrenal Glands / blood supply. Adrenocortical Adenoma / blood. Aldosterone / blood. Hyperaldosteronism / blood

  • Genetic Alliance. consumer health - Primary aldosteronism.
  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18176003.001).
  • [ISSN] 1349-7235
  • [Journal-full-title] Internal medicine (Tokyo, Japan)
  • [ISO-abbreviation] Intern. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 4964P6T9RB / Aldosterone
  •  go-up   go-down


96. Bouyahia O, Gharsallah L, Ouederni M, Boukthir S, Mrad SM, El Gharbi AS: Feminizing adrenocortical adenoma in a 5 year-old girl. J Pediatr Endocrinol Metab; 2009 Jan;22(1):79-84
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Feminizing adrenocortical adenoma in a 5 year-old girl.
  • Adrenocortical adenoma is a rare etiology of isosexual precocious puberty in girls.
  • We report the case of a 5 year-old girl with isosexual precocious puberty.
  • Pathological examination after complete surgical resection showed an adrenocortical adenoma.
  • The diagnosis of feminizing adrenocortical adenoma was confirmed.
  • [MeSH-major] Adrenal Cortex Neoplasms / complications. Adrenocortical Adenoma / complications. Puberty, Precocious / etiology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19344078.001).
  • [ISSN] 0334-018X
  • [Journal-full-title] Journal of pediatric endocrinology & metabolism : JPEM
  • [ISO-abbreviation] J. Pediatr. Endocrinol. Metab.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  •  go-up   go-down


97. Lim YJ, Lee SM, Shin JH, Koh HC, Lee YH: Virilizing adrenocortical oncocytoma in a child: a case report. J Korean Med Sci; 2010 Jul;25(7):1077-9
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Virilizing adrenocortical oncocytoma in a child: a case report.
  • Functioning adrenocortical oncocytomas are extremely rare and most reported patients are 40-60 yr of age.
  • To our knowledge, only 2 cases of functioning adrenocortical oncocytomas have been reported in childhood.
  • We report a case of functioning adrenocortical oncocytoma in a 14-yr-old female child presenting with virilization.
  • [MeSH-major] Adenoma, Oxyphilic / complications. Adrenal Cortex Neoplasms / complications. Virilism / etiology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Int J Surg Pathol. 2003 Oct;11(4):325-9 [14615833.001]
  • [Cites] J Clin Oncol. 2004 Mar 1;22(5):838-45 [14990639.001]
  • [Cites] Int J Surg Pathol. 2004 Jul;12(3):231-43 [15306935.001]
  • [Cites] J Pediatr Surg. 2008 May;43(5):E1-3 [18485928.001]
  • [Cites] Best Pract Res Clin Endocrinol Metab. 2006 Jun;20(2):167-76 [16772149.001]
  • [Cites] Urol Oncol. 2008 Mar-Apr;26(2):198-201 [18312941.001]
  • [Cites] Urol Clin North Am. 1989 Aug;16(3):469-79 [2665273.001]
  • (PMID = 20592902.001).
  • [ISSN] 1598-6357
  • [Journal-full-title] Journal of Korean medical science
  • [ISO-abbreviation] J. Korean Med. Sci.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2890887
  • [Keywords] NOTNLM ; Adenoma, Oxyphilic / Adrenal Cortex Neoplasms / Child / Virilism
  •  go-up   go-down


98. Liao CH, Chueh SC, Lai MK, Hsiao PJ, Chen J: Laparoscopic adrenalectomy for potentially malignant adrenal tumors greater than 5 centimeters. J Clin Endocrinol Metab; 2006 Aug;91(8):3080-3
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Laparoscopic adrenalectomy for potentially malignant adrenal tumors greater than 5 centimeters.
  • PURPOSE: Laparoscopic adrenalectomy (LA) is controversial for large, potentially malignant tumors.
  • We report a series of LA or hand-assisted LA for large (>5 cm) adrenal tumors.
  • Final pathology revealed eight malignant (four adrenocortical carcinomas and four metastatic carcinomas) and 31 benign tumors (14 cortical adenomas, eight pheochromocytomas, six myelolipomas, and three ganglioneuromas).
  • Four patients (two adrenocortical carcinomas, one metastatic hepatoma, and one lymphoma) died 24, 10, 9, and 3 months after surgery, respectively.
  • CONCLUSIONS: LA is a reasonable option for selected large adrenal tumors when complete resection is technically feasible and there is no evidence of local invasion.
  • Hand-assisted LA is a good alternative to open conversion if a difficult dissection is encountered intraoperatively.
  • [MeSH-major] Adrenal Gland Neoplasms / pathology. Adrenal Gland Neoplasms / surgery. Adrenalectomy / methods. Laparoscopy
  • [MeSH-minor] Adenoma / pathology. Adenoma / surgery. Adolescent. Adult. Aged. Child. Child, Preschool. Ganglioneuroma / pathology. Ganglioneuroma / surgery. Humans. Middle Aged. Myelolipoma / pathology. Myelolipoma / surgery. Neoplasm Metastasis. Pheochromocytoma / pathology. Pheochromocytoma / surgery. Prognosis. Survival Rate

  • MedlinePlus Health Information. consumer health - Adrenal Gland Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [CommentIn] Nat Clin Pract Endocrinol Metab. 2007 Mar;3(3):210-1 [17262068.001]
  • (PMID = 16720665.001).
  • [ISSN] 0021-972X
  • [Journal-full-title] The Journal of clinical endocrinology and metabolism
  • [ISO-abbreviation] J. Clin. Endocrinol. Metab.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


99. Cotesta D, Caliumi C, Alò P, Petramala L, Reale MG, Masciangelo R, Signore A, Cianci R, D'Erasmo E, Letizia C: High plasma levels of human chromogranin A and adrenomedullin in patients with pheochromocytoma. Tumori; 2005 Jan-Feb;91(1):53-8
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • METHODS AND STUDY DESIGN: We collected blood samples for measurement of plasma CgA and AM in 21 patients with pheochromocytomas, 43 healthy subjects and 26 patients with solid non-functioning adrenocortical adenomas.
  • CgA and AM were measured by means of a novel solid-phase two-site immunoradiometric assay based on monoclonal antibodies (CgA-RIA CT, CIS bio international) and by a specific radioimmunoassay (RIA, Phoenix Pharm. Inc.
  • RESULTS: The mean plasma CgA level (+/- SD) in patients with pheochromocytomas (204 +/- 147.9 ng/mL) was significantly higher (P < 0.001) than that in healthy subjects (41.6 +/- 10.7 ng/mL) and in patients with non-functioning adrenocortical adenomas (47.3 +/- 17.6 ng/mL).
  • The mean plasma AM concentration (+/- SD) in patients with pheochromocytomas (27.5 +/- 10.4 pg/mL) was significantly higher (P < 0.001) than that in HS (13.8 +/- 4.5 pg/mL) and in patients with non-functioning adrenocortical adenomas (16.6 +/- 7.3 pg/mL).
  • CONCLUSION: This study demonstrates that circulating CgA and AM levels are increased in pheochromocytoma patients compared with healthy subjects and patients with non-functioning adrenocortical adenomas.
  • Moreover, at the time of diagnosis plasma CgA levels correlated with plasma AM levels and with plasma metanephrine levels in all patients with pheochromocytomas.
  • [MeSH-major] Adrenal Gland Neoplasms / blood. Biomarkers, Tumor / blood. Chromogranins / blood. Peptides / blood. Pheochromocytoma / blood
  • [MeSH-minor] Adrenal Cortex Neoplasms / blood. Adrenocortical Adenoma / blood. Adrenomedullin. Adult. Antibodies, Monoclonal. Chromogranin A. Female. Humans. Immunohistochemistry. Male. Middle Aged. Radioimmunoassay. Sensitivity and Specificity. Tissue Distribution

  • Genetic Alliance. consumer health - Pheochromocytoma.
  • MedlinePlus Health Information. consumer health - Adrenal Gland Cancer.
  • MedlinePlus Health Information. consumer health - Pheochromocytoma.
  • NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15850005.001).
  • [ISSN] 0300-8916
  • [Journal-full-title] Tumori
  • [ISO-abbreviation] Tumori
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Biomarkers, Tumor; 0 / CHGA protein, human; 0 / Chromogranin A; 0 / Chromogranins; 0 / Peptides; 148498-78-6 / Adrenomedullin
  •  go-up   go-down


100. Bimpaki EI, Nesterova M, Stratakis CA: Abnormalities of cAMP signaling are present in adrenocortical lesions associated with ACTH-independent Cushing syndrome despite the absence of mutations in known genes. Eur J Endocrinol; 2009 Jul;161(1):153-61
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Abnormalities of cAMP signaling are present in adrenocortical lesions associated with ACTH-independent Cushing syndrome despite the absence of mutations in known genes.
  • CONTEXT: Bilateral adrenal hyperplasias (BAHs) may be caused by mutations of genes that code for molecules that participate in cAMP signaling.
  • Little is known about cAMP signaling in adrenal lesions associated with ACTH-independent Cushing syndrome (AICS) that do not harbor mutations in known genes.
  • DESIGN: Samples from 27 patients (ages 5-60 years) were studied and compared with normal adrenocortical tissue (n=4) and aldosterone-producing adenomas (APA, n=5).
  • RESULTS: Cortisol-producing adenomas (CPAs) and other lesions that were GNAS, PRKAR1A, PDE11A, and PDE8B gene mutation-negative were compared with PRKAR1A mutation-positive lesions, normal tissue, and APAs; abnormalities of the cAMP-signaling pathway were found in both BAHs and CPAs.
  • CONCLUSION: Lesions of the adrenal associated with AICS, independently of their GNAS, PRKAR1A, PDE11A, and PDE8B mutation status, have functional abnormalities of cAMP signaling.

  • Genetic Alliance. consumer health - Cushing's Syndrome.
  • MedlinePlus Health Information. consumer health - Cushing's Syndrome.
  • Hazardous Substances Data Bank. HYDROCORTISONE .
  • Hazardous Substances Data Bank. Corticotropin .
  • antibodies-online. View related products from antibodies-online.com (subscription/membership/fee required).
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] J Clin Endocrinol Metab. 2003 May;88(5):2147-51 [12727968.001]
  • [Cites] Cancer Res. 2003 Sep 1;63(17):5308-19 [14500362.001]
  • [Cites] Proc Natl Acad Sci U S A. 1970 Sep;67(1):305-12 [4318781.001]
  • [Cites] Biochim Biophys Acta. 1975 Feb 19;377(2):271-81 [235302.001]
  • [Cites] J Clin Endocrinol Metab. 1994 Sep;79(3):890-3 [8077378.001]
  • [Cites] J Clin Endocrinol Metab. 2005 Mar;90(3):1302-10 [15585558.001]
  • [Cites] J Clin Endocrinol Metab. 2000 Oct;85(10):3531-6 [11061496.001]
  • [Cites] Nat Genet. 2000 Sep;26(1):89-92 [10973256.001]
  • [Cites] Am J Hum Genet. 2002 Dec;71(6):1433-42 [12424709.001]
  • [Cites] J Clin Endocrinol Metab. 2002 Sep;87(9):4324-9 [12213893.001]
  • [Cites] J Clin Endocrinol Metab. 2006 May;91(5):1943-9 [16464939.001]
  • [Cites] Clin Cancer Res. 2008 Jun 15;14(12):4016-24 [18559625.001]
  • [Cites] Eur J Hum Genet. 2008 Oct;16(10):1245-53 [18431404.001]
  • [Cites] Nat Genet. 2006 Jul;38(7):794-800 [16767104.001]
  • [Cites] J Clin Endocrinol Metab. 2006 Sep;91(9):3626-32 [16772351.001]
  • [Cites] Cancer Res. 2006 Dec 15;66(24):11571-5 [17178847.001]
  • [Cites] Curr Opin Endocrinol Diabetes Obes. 2007 Jun;14(3):219-25 [17940443.001]
  • [Cites] Nat Clin Pract Endocrinol Metab. 2007 Nov;3(11):748-57 [17955016.001]
  • [Cites] J Clin Endocrinol Metab. 2008 Feb;93(2):565-71 [18056771.001]
  • [Cites] N Engl J Med. 2008 Feb 14;358(7):750-2 [18272904.001]
  • [Cites] Horm Metab Res. 2008 May;40(5):347-53 [18491255.001]
  • [Cites] Endocr Dev. 2008;13:117-32 [18493137.001]
  • (PMID = 19429701.001).
  • [ISSN] 1479-683X
  • [Journal-full-title] European journal of endocrinology
  • [ISO-abbreviation] Eur. J. Endocrinol.
  • [Language] ENG
  • [Grant] United States / NICHD NIH HHS / HD / Z01 HD000642; United States / Intramural NIH HHS / / ZIA HD000642-13; United States / NICHD NIH HHS / HD / Z01-HD-000642-04
  • [Publication-type] Journal Article; Research Support, N.I.H., Intramural; Research Support, U.S. Gov't, P.H.S.
  • [Publication-country] England
  • [Chemical-registry-number] 0 / CREBBP protein, human; 0 / Cyclic AMP-Dependent Protein Kinase RIalpha Subunit; 0 / PRKAR1A protein, human; 9002-60-2 / Adrenocorticotropic Hormone; E0399OZS9N / Cyclic AMP; EC 2.3.1.48 / CREB-Binding Protein; EC 2.7.11.11 / Cyclic AMP-Dependent Protein Kinases; EC 3.1.4.- / Phosphoric Diester Hydrolases; EC 3.1.4.17 / 3',5'-Cyclic-AMP Phosphodiesterases; EC 3.1.4.17 / PDE8B protein, human; EC 3.1.4.35 / PDE11A protein, human; EC 3.6.1.- / GNAS protein, human; EC 3.6.5.1 / GTP-Binding Protein alpha Subunits, Gs; WI4X0X7BPJ / Hydrocortisone
  • [Other-IDs] NLM/ NIHMS305405; NLM/ PMC3136809
  •  go-up   go-down






Advertisement