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309 related items for PubMed ID: 17100132
1. [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. PubMed ID: 17100132 [Abstract] [Full Text] [Related]
2. [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 Oct 28; 128(9-10):268-73. PubMed ID: 17128664 [Abstract] [Full Text] [Related]
3. 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 28; 61(5):553-9. PubMed ID: 15521956 [Abstract] [Full Text] [Related]
4. Bilateral adrenal Cushing's syndrome: macronodular adrenal hyperplasia and primary pigmented nodular adrenocortical disease. Lacroix A, Bourdeau I. Endocrinol Metab Clin North Am; 2005 Jun 28; 34(2):441-58, x. PubMed ID: 15850852 [Abstract] [Full Text] [Related]
5. 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 28; 87(9):4324-9. PubMed ID: 12213893 [Abstract] [Full Text] [Related]
6. [Primary pigmented nodular adrenocortical dysplasia. A rare cause of Cushing's syndrome]. Anding K, Köhler G, Böhm N, Petersen KG, Schollmeyer P, Neumann HP. Dtsch Med Wochenschr; 1996 Oct 25; 121(43):1321-4. PubMed ID: 8964212 [Abstract] [Full Text] [Related]
7. PRKAR1A-negative familial Cushing's syndrome: two case reports. Lim LL, Kitan N, Paramasivam SS, Ratnasingam J, Ibrahim L, Chan SP, Tan AT, Vethakkan SR. J Med Case Rep; 2015 Dec 01; 9():277. PubMed ID: 26619967 [Abstract] [Full Text] [Related]
8. 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 01; 27(9-10):1005-9. PubMed ID: 24859511 [Abstract] [Full Text] [Related]
17. Familial ACTH-independent Cushing's syndrome with bilateral macronodular adrenal hyperplasia clinically affecting only female family members. Nies C, Bartsch DK, Ehlenz K, Wild A, Langer P, Fleischhacker S, Rothmund M. Exp Clin Endocrinol Diabetes; 2002 Sep 01; 110(6):277-83. PubMed ID: 12373631 [Abstract] [Full Text] [Related]
18. Bilateral Adrenocortical Nodular Disease and Cushing's Syndrome. Bouys L, Violon F, Louiset E, Sibony M, Lefebvre H, Bertherat J. J Clin Endocrinol Metab; 2024 Sep 16; 109(10):2422-2432. PubMed ID: 38888184 [Abstract] [Full Text] [Related]
19. Primary pigmented nodular adrenocortical disease: the original 4 cases revisited after 30 years for follow-up, new investigations, and molecular genetic findings. Carney JA, Libé R, Bertherat J, Young WF. Am J Surg Pathol; 2014 Sep 16; 38(9):1266-73. PubMed ID: 24805858 [Abstract] [Full Text] [Related]