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145 related items for PubMed ID: 35649622

  • 1. Primary pigmented nodular adrenal disease presenting as hypertensive crisis.
    Oza CM, Mehta S, Khadilkar V, Khadilkar A.
    BMJ Case Rep; 2022 Jun 01; 15(6):. PubMed ID: 35649622
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Efficacy of dexamethasone suppression test during the diagnosis of primary pigmented nodular adrenocortical disease in Chinese adrenocorticotropic hormone-independent Cushing syndrome.
    Chen S, Li R, Lu L, Duan L, Zhang X, Tong A, Pan H, Zhu H, Lu Z.
    Endocrine; 2018 Jan 01; 59(1):183-190. PubMed ID: 29094256
    [Abstract] [Full Text] [Related]

  • 4. [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]

  • 5. Primary pigmented nodular adrenocortical disease: paradoxical responses of cortisol secretion to dexamethasone occur in vitro and are associated with increased expression of the glucocorticoid receptor.
    Bourdeau I, Lacroix A, Schürch W, Caron P, Antakly T, Stratakis CA.
    J Clin Endocrinol Metab; 2003 Aug 28; 88(8):3931-7. PubMed ID: 12915689
    [Abstract] [Full Text] [Related]

  • 6. Causes and consequences of abandoning one-stage bilateral adrenalectomy recommended in primary pigmented nodular adrenocortical disease--case presentation.
    Kumorowicz-Czoch M, Dolezal-Oltarzewska K, Roztoczynska D, Chrupek M, Prokurat AI, Drabik G, Starzyk J.
    J Pediatr Endocrinol Metab; 2011 Aug 28; 24(7-8):565-7. PubMed ID: 21932601
    [Abstract] [Full Text] [Related]

  • 7. Bilateral adrenocortical adenomas causing ACTH-independent Cushing's syndrome at different periods: a case report and discussion of corticosteroid replacement therapy following bilateral adrenalectomy.
    Tung SC, Wang PW, Huang TL, Lee WC, Chen WJ.
    J Endocrinol Invest; 2004 Apr 28; 27(4):375-9. PubMed ID: 15233560
    [Abstract] [Full Text] [Related]

  • 8. Germline PRKACA amplification-associated primary pigmented nodular adrenocortical disease: a case report and literature review.
    Yang WR, Liang XH, Qin YF, Yang HY, He SZ, Huang ZX, Liu YP, Luo ZJ.
    Arch Endocrinol Metab; 2023 Nov 17; 68():e220491. PubMed ID: 37988664
    [Abstract] [Full Text] [Related]

  • 9. 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 17; 34(12):1022-1026. PubMed ID: 30129786
    [Abstract] [Full Text] [Related]

  • 10. The role of unilateral adrenalectomy in corticotropin-independent bilateral adrenocortical hyperplasias.
    Xu Y, Rui W, Qi Y, Zhang C, Zhao J, Wang X, Wu Y, Zhu Q, Shen Z, Ning G, Zhu Y.
    World J Surg; 2013 Jul 17; 37(7):1626-32. PubMed ID: 23592061
    [Abstract] [Full Text] [Related]

  • 11. Use of 3-Dimensional Volumetric Modeling of Adrenal Gland Size in Patients with Primary Pigmented Nodular Adrenocortical Disease.
    Chrysostomou PP, Lodish MB, Turkbey EB, Papadakis GZ, Stratakis CA.
    Horm Metab Res; 2016 Apr 17; 48(4):242-6. PubMed ID: 27065461
    [Abstract] [Full Text] [Related]

  • 12. 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 Apr 17; 59(9):823-30. PubMed ID: 22785148
    [Abstract] [Full Text] [Related]

  • 13. 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 17; 89(7):3173-82. PubMed ID: 15240590
    [Abstract] [Full Text] [Related]

  • 14. Cushing syndrome: uncovering Carney complex due to novel PRKAR1A mutation.
    Zhang CD, Pichurin PN, Bobr A, Lyden ML, Young WF, Bancos I.
    Endocrinol Diabetes Metab Case Rep; 2019 Mar 21; 2019():. PubMed ID: 30897549
    [Abstract] [Full Text] [Related]

  • 15. 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 21; 61(5):553-9. PubMed ID: 15521956
    [Abstract] [Full Text] [Related]

  • 16. 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 21; 16(1):84-8. PubMed ID: 19703806
    [Abstract] [Full Text] [Related]

  • 17. An unusual cause of Cushing's syndrome: primary pigmented nodular adrenal dysplasia.
    Sofat N, Turner J, Khoo B, Sohail M, Krausz T, Evans P, Meeran K.
    Int J Clin Pract; 2000 May 21; 54(4):269-71. PubMed ID: 10912321
    [Abstract] [Full Text] [Related]

  • 18. 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 21; 10(1):68-72. PubMed ID: 7626560
    [Abstract] [Full Text] [Related]

  • 19. Cushing´s syndrome due to bilateral adrenal cortical disease: Bilateral macronodular adrenal cortical disease and bilateral micronodular adrenal cortical disease.
    Araujo-Castro M, Marazuela M.
    Front Endocrinol (Lausanne); 2022 Jan 21; 13():913253. PubMed ID: 35992106
    [Abstract] [Full Text] [Related]

  • 20. Challenging Diagnostic Workup of a 22-year-old Patient With Primary Pigmented Nodular Adrenocortical Disease.
    Wernig J, Pilz S, Trummer C, Theiler-Schwetz V, Schmitt LM, Tsybrovskyy O.
    JCEM Case Rep; 2024 Oct 21; 2(10):luae174. PubMed ID: 39355138
    [Abstract] [Full Text] [Related]

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