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Journal Abstract Search

151 related items for PubMed ID: 9587940

  • 41. Cushing's syndrome due to primary pigmented nodular adrenocortical disease with cardiac myxomas and mucocutaneous lentigines.
    Ichiba Y, Nishizaki Y, Tanizaki M.
    Acta Paediatr; 1992 Jan; 81(1):91-2. PubMed ID: 1600314
    [Abstract] [Full Text] [Related]

  • 42. 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. PubMed ID: 24859511
    [Abstract] [Full Text] [Related]

  • 43. 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 07; 124(6):336-9. PubMed ID: 17322955
    [Abstract] [Full Text] [Related]

  • 44. Carney's complex of primary pigmented nodular adrenocortical disease and pigmentous and myxomatous lesions.
    Cheung PS, Thompson NW.
    Surg Gynecol Obstet; 1989 May 07; 168(5):413-6. PubMed ID: 2711295
    [Abstract] [Full Text] [Related]

  • 45. Clinical and genetic analysis of primary bilateral adrenal diseases (micro- and macronodular disease) leading to Cushing syndrome.
    Stratakis CA, Kirschner LS.
    Horm Metab Res; 1998 May 07; 30(6-7):456-63. PubMed ID: 9694579
    [Abstract] [Full Text] [Related]

  • 46. 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 07; 38(9):1266-73. PubMed ID: 24805858
    [Abstract] [Full Text] [Related]

  • 47. [ACTH-independent bilateral adrenocortical macronodular hyperplasia (AIMAH): report of a case].
    Nakano M, Tada K, Takahashi Y, Deguchi T, Kuriyama M, Ban Y, Kawada Y, Hanafusa J, Morita H, Yasuda K.
    Hinyokika Kiyo; 1995 Jul 07; 41(7):529-32. PubMed ID: 7668183
    [Abstract] [Full Text] [Related]

  • 48. Successful pregnancy after unilateral adrenalectomy in a case of primary pigmented adrenocortical disease.
    Cohen O, Bogat S, Dolitzki M, Karasik A.
    J Matern Fetal Neonatal Med; 2005 Feb 07; 17(2):161-3. PubMed ID: 16076627
    [Abstract] [Full Text] [Related]

  • 49. Familial Cushing's syndrome due to pigmented multinodular adrenocortical dysplasia.
    Böhm N, Lippmann-Grob B, von Petrykowski W.
    Acta Endocrinol (Copenh); 1983 Mar 07; 102(3):428-35. PubMed ID: 6219529
    [Abstract] [Full Text] [Related]

  • 50. Histopathology and ultrastructure of primary adrenocortical nodular dysplasia with Cushing's syndrome.
    Iseli BE, Hedinger CE.
    Histopathology; 1985 Nov 07; 9(11):1171-94. PubMed ID: 4085982
    [Abstract] [Full Text] [Related]

  • 51. Cushing syndrome in a young woman due to primary pigmented nodular adrenal disease.
    Hackman KL, Davis AL, Curnow PA, Serpell JW, McLean CA, Topliss DJ.
    Endocr Pract; 2010 Nov 07; 16(1):84-8. PubMed ID: 19703806
    [Abstract] [Full Text] [Related]

  • 52. [Adrenocortical macronodular hyperplasia with massive enlargement of the gland. A rare variant of autonomous hypercortisolism].
    Redondo E, Rey A, Rivero L, Sánchez-Moro V, Marín J, Rivero JC, Sánchez-Lobo V.
    Arch Esp Urol; 2001 Jun 07; 54(5):458-63. PubMed ID: 11494723
    [Abstract] [Full Text] [Related]

  • 53. The clinical characteristics and pathogenic variants of primary pigmented nodular adrenocortical disease in 210 patients: a systematic review.
    Sun J, Ding L, He L, Fu H, Li R, Feng J, Dong J, Liao L.
    Front Endocrinol (Lausanne); 2024 Jun 07; 15():1356870. PubMed ID: 39006359
    [Abstract] [Full Text] [Related]

  • 54. Familial micronodular adrenocortical disease, Cushing syndrome, and mutations of the gene encoding phosphodiesterase 11A4 (PDE11A).
    Carney JA, Gaillard RC, Bertherat J, Stratakis CA.
    Am J Surg Pathol; 2010 Apr 07; 34(4):547-55. PubMed ID: 20351491
    [Abstract] [Full Text] [Related]

  • 55. Primary pigmented nodular adrenocortical disease (PPNAD) as an underlying cause of symptoms in a patient presenting with hirsutism and secondary amenorrhea: case report and literature review.
    Cyranska-Chyrek E, Filipowicz D, Szczepanek-Parulska E, Nowaczyk M, Ambroziak U, Toutounchi S, Koperski Ł, Bednarczuk T, Meczekalski B, Ruchała M.
    Gynecol Endocrinol; 2018 Dec 07; 34(12):1022-1026. PubMed ID: 30129786
    [Abstract] [Full Text] [Related]

  • 56. Primary pigmented nodular adrenocortical dysplasia: a rare form of a rare disorder.
    Jabbar A, Grant D, Savage M, Grossman A.
    J R Soc Med; 1994 Feb 07; 87(2):110-1. PubMed ID: 8196028
    [No Abstract] [Full Text] [Related]

  • 57. Cushing's syndrome due to primary pigmented nodular adrenal disease in two brothers with Carney complex.
    Attri B, Aggarwal A, Mattoo S, Kulshreshtha B.
    Pediatr Endocrinol Diabetes Metab; 2020 Feb 07; 26(3):155-158. PubMed ID: 32901471
    [Abstract] [Full Text] [Related]

  • 58. Carney's complex with primary pigmented nodular adrenocortical disease and spotty pigmentations.
    Ohara N, Komiya I, Yamauchi K, Ohtsuka H, Nagasawa Y, Takeda T, Takasu N.
    Intern Med; 1993 Jan 07; 32(1):60-2. PubMed ID: 8495049
    [Abstract] [Full Text] [Related]

  • 59. Corticotropinoma as the underlying cause of intermittent Cushing's syndrome in a patient previously diagnosed with primary pigmented nodular adrenocortical disease.
    Łebek-Szatańska A, Stelmachowska-Banaś M, Zieliński G, Styk A, Nowak KM, Papierska L.
    Endokrynol Pol; 2020 Jan 07; 71(3):273-274. PubMed ID: 32293705
    [Abstract] [Full Text] [Related]

  • 60. Multiple pigmented adrenal cortical nodules associated with Cushing's syndrome. Histochemical, ultrastructural and quantitative studies.
    Kawai K, Shigematsu K, Matsuo K, Tsuchiyama H, Saito Y.
    Acta Pathol Jpn; 1984 Jul 07; 34(4):827-37. PubMed ID: 6592938
    [Abstract] [Full Text] [Related]

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