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Similar articles for PubMed (Select 24859511)

1.

A rare case of familial Cushing's syndrome with a common presentation of weight gain due to a mutation of the PRKAR1A gene causing isolated primary pigmented nodular adrenocortical disease.

Poukoulidou T, Maiter D, Bertherat J, Beauloye V.

J Pediatr Endocrinol Metab. 2014 Sep;27(9-10):1005-9. doi: 10.1515/jpem-2014-0018.

PMID:
24859511
2.

Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease.

Groussin L, Jullian E, Perlemoine K, Louvel A, Leheup B, Luton JP, Bertagna X, Bertherat J.

J Clin Endocrinol Metab. 2002 Sep;87(9):4324-9.

PMID:
12213893
3.

PRKAR1A mutations in primary pigmented nodular adrenocortical disease.

Cazabat L, Ragazzon B, Groussin L, Bertherat J.

Pituitary. 2006;9(3):211-9. Review.

PMID:
17036196
4.

A novel PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease and the Carney complex.

Peck MC, Visser BC, Norton JA, Pasche L, Katznelson L.

Endocr Pract. 2010 Mar-Apr;16(2):198-204. doi: 10.4158/EP09245.OR.

PMID:
19833579
5.

[A girl with Cushing's syndrome due to primary pigmented nodular adrenocortical disease].

Bocca G, van Mil EG, Voorhoeve PG, Wijnaendts LC, Delemarre-van de Waal HA.

Ned Tijdschr Geneeskd. 2006 Oct 28;150(43):2390-3. Dutch.

PMID:
17100132
6.

Adrenal pathophysiology: lessons from the Carney complex.

Groussin L, Cazabat L, René-Corail F, Jullian E, Bertherat J.

Horm Res. 2005;64(3):132-9. Epub 2005 Sep 27. Review.

7.

Carney complex, a familial Cushing's syndrome due to primary pigmented nodular adrenocortical disease: a case report.

Hsin SC, Hsieh MC, Hwang SJ, Hsia PJ, Tsay KB, Shin SL.

Kaohsiung J Med Sci. 2002 Dec;18(12):627-31.

PMID:
12670039
8.

Primary pigmented nodular adrenocortical disease presenting with a unilateral adrenocortical nodule treated with bilateral laparoscopic adrenalectomy: a case report.

Zografos GN, Pappa T, Avlonitis S, Markou A, Chrysikos DT, Kaltsas G, Aggeli C, Piaditis G.

J Med Case Rep. 2010 Jul 29;4:230. doi: 10.1186/1752-1947-4-230.

10.

Primary pigmented nodular adrenocortical disease associated with Carney complex: case report and literature review.

Gonçalves FT, Feibelmann TC, Mendes CM, Fernandes ML, Miranda GH, Gouvêa AP, Jorge PT.

Sao Paulo Med J. 2006 Nov 7;124(6):336-9. Review.

11.

Familial isolated primary pigmented nodular adrenocortical disease associated with a novel low penetrance PRKAR1A gene splice site mutation.

Storr HL, Metherell LA, Dias R, Savage MO, Rasmussen AK, Clark AJ, Main KM.

Horm Res Paediatr. 2010;73(2):115-9. doi: 10.1159/000277629. Epub 2010 Feb 9.

PMID:
20190548
12.

[A pedigree study of a patient with primary pigmented nodular adrenocortical disease and familial gene mutation].

Ran H, Ma X, Wang Q, Xie Z, Ding Y, Qin G.

Zhonghua Nei Ke Za Zhi. 2014 May;53(5):398-402. Chinese.

PMID:
25146409
13.

Children with Cushing's syndrome: Primary Pigmented Nodular Adrenocortical Disease should always be suspected.

da Silva RM, Pinto E, Goldman SM, Andreoni C, Vieira TC, Abucham J.

Pituitary. 2011 Mar;14(1):61-7. doi: 10.1007/s11102-010-0260-5.

PMID:
20924687
14.

[Primary pigmented nodular adrenocortical disease as cause of Cushing's syndrome associated with Carney complex].

Dumić M, Janjanin N, Uroić AS, Ille J, Skegro M, Kusec V, Marjanac I, Matić T, Jelasić D.

Lijec Vjesn. 2006 Sep-Oct;128(9-10):268-73. Croatian.

PMID:
17128664
15.

Association of the M1V PRKAR1A mutation with primary pigmented nodular adrenocortical disease in two large families.

Pereira AM, Hes FJ, Horvath A, Woortman S, Greene E, Bimpaki E, Alatsatianos A, Boikos S, Smit JW, Romijn JA, Nesterova M, Stratakis CA.

J Clin Endocrinol Metab. 2010 Jan;95(1):338-42. doi: 10.1210/jc.2009-0993. Epub 2009 Nov 13.

16.

Carney complex presenting with a unilateral adrenocortical nodule: a case report.

Talaei A, Aminorroaya A, Taheri D, Mahdavi KN.

J Med Case Rep. 2014 Feb 5;8:38. doi: 10.1186/1752-1947-8-38.

17.

Cushing's syndrome due to bilateral adrenocortical adenomas with unique histological features.

Nomura K, Saito H, Aiba M, Iihara M, Obara T, Takano K.

Endocr J. 2003 Apr;50(2):155-62.

18.

Carney complex (CNC).

Bertherat J.

Orphanet J Rare Dis. 2006 Jun 6;1:21. Review.

19.

Clinical features, diagnosis, treatment and molecular studies in paediatric Cushing's syndrome due to primary nodular adrenocortical hyperplasia.

Storr HL, Mitchell H, Swords FM, Main KM, Hindmarsh PC, Betts PR, Shaw NJ, Johnston DI, Clark AJ, Reznek RH, Grossman AB, Savage MO.

Clin Endocrinol (Oxf). 2004 Nov;61(5):553-9.

PMID:
15521956
20.

Cyclical Cushing syndrome presenting in infancy: an early form of primary pigmented nodular adrenocortical disease, or a new entity?

Gunther DF, Bourdeau I, Matyakhina L, Cassarino D, Kleiner DE, Griffin K, Courkoutsakis N, Abu-Asab M, Tsokos M, Keil M, Carney JA, Stratakis CA.

J Clin Endocrinol Metab. 2004 Jul;89(7):3173-82.

PMID:
15240590
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