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Journal Abstract Search

184 related items for PubMed ID: 20351491

  • 21.
    ; . PubMed ID:
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  • 22. Primary pigmented nodular adrenocortical dysplasia.
    Köhler G, Anding K, Böhm N.
    Pathol Res Pract; 1998; 194(3):201-4. PubMed ID: 9587940
    [Abstract] [Full Text] [Related]

  • 23. Primary pigmented nodular adrenocortical disease and Cushing's syndrome.
    Horvath A, Stratakis C.
    Arq Bras Endocrinol Metabol; 2007 Nov; 51(8):1238-44. PubMed ID: 18209861
    [Abstract] [Full Text] [Related]

  • 24. 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. PubMed ID: 12213893
    [Abstract] [Full Text] [Related]

  • 25. A Novel Mutation in the type Iα Regulatory Subunit of Protein Kinase A (PRKAR1A) in a Cushing's Syndrome Patient with Primary Pigmented Nodular Adrenocortical Disease.
    Mineo R, Tamba S, Yamada Y, Okita T, Kawachi Y, Mori R, Kyo M, Saisho K, Kuroda Y, Yamamoto K, Furuya A, Mukai T, Maekawa T, Nakamura Y, Sasano H, Matsuzawa Y.
    Intern Med; 2016 Sep; 55(17):2433-8. PubMed ID: 27580546
    [Abstract] [Full Text] [Related]

  • 26. Bilateral primary pigmented nodular adrenocortical disease. Rare cause of the Cushing syndrome.
    Shenoy BV, Carpenter PC, Carney JA.
    Am J Surg Pathol; 1984 May; 8(5):335-44. PubMed ID: 6329005
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  • 27.
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  • 28. Familial Cushing's syndrome due to nodular adrenocortical dysplasia. A putative receptor-antibody disease?
    Teding van Berkhout F, Croughs RJ, Kater L, Schuurman HJ, Gmelig Meyling FJ, Kooyman CD, van der Gaag RD, Jolink D, Drexhage HA.
    Clin Endocrinol (Oxf); 1986 Mar; 24(3):299-310. PubMed ID: 3708877
    [Abstract] [Full Text] [Related]

  • 29. Cushing's syndrome due to primary pigmented nodular adrenocortical disease--a case report reviews of the literature.
    Choi KM, Seu JH, Kim YH, Lee EJ, Kim SJ, Baik SH, Choi DS.
    Korean J Intern Med; 1995 Jan; 10(1):68-72. PubMed ID: 7626560
    [Abstract] [Full Text] [Related]

  • 30.
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  • 31. Operative management of Cushing syndrome secondary to micronodular adrenal hyperplasia.
    Powell AC, Stratakis CA, Patronas NJ, Steinberg SM, Batista D, Alexander HR, Pingpank JF, Keil M, Bartlett DL, Libutti SK.
    Surgery; 2008 Jun; 143(6):750-8. PubMed ID: 18549891
    [Abstract] [Full Text] [Related]

  • 32. Adrenal hyperplasias in childhood: An update.
    Pitsava G, Stratakis CA.
    Front Endocrinol (Lausanne); 2022 Jun; 13():937793. PubMed ID: 35992119
    [Abstract] [Full Text] [Related]

  • 33. New genes and/or molecular pathways associated with adrenal hyperplasias and related adrenocortical tumors.
    Stratakis CA.
    Mol Cell Endocrinol; 2009 Mar 05; 300(1-2):152-7. PubMed ID: 19063937
    [Abstract] [Full Text] [Related]

  • 34. An unusual presentation of Carney complex with diffuse primary pigmented nodular adrenocortical disease on one adrenal gland and a nonpigmented adrenocortical adenoma and focal primary pigmented nodular adrenocortical disease on the other.
    Tung SC, Hwang DY, Yang JW, Chen WJ, Lee CT.
    Endocr J; 2012 Mar 05; 59(9):823-30. PubMed ID: 22785148
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. 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 Mar 05; 73(2):115-9. PubMed ID: 20190548
    [Abstract] [Full Text] [Related]

  • 37. Familial Cushing's syndrome. Micronodular adrenocortical dysplasia.
    Hodge BO, Froesch TA.
    Arch Intern Med; 1988 May 05; 148(5):1133-6. PubMed ID: 3365080
    [Abstract] [Full Text] [Related]

  • 38. Phosphodiesterases and adrenal Cushing in mice and humans.
    Szarek E, Stratakis CA.
    Horm Metab Res; 2014 Nov 05; 46(12):863-8. PubMed ID: 25232906
    [Abstract] [Full Text] [Related]

  • 39. Primary pigmented nodular adrenocortical disease: literature review and case report of a 6-year-old boy.
    Katanić D, Kafka D, Živojinov M, Vlaški J, Budakov Z, Knežević Pogančev M, Vorgučin I, Ćuk T.
    J Pediatr Endocrinol Metab; 2017 May 01; 30(5):603-609. PubMed ID: 28391254
    [Abstract] [Full Text] [Related]

  • 40. 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]

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