BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 35925470)

  • 1. Unilateral or bilateral adrenalectomy in PPNAD: six cases from a single family followed up over 40 years.
    Vitellius G; Donadille B; Decoudier B; Leroux A; Deguelte S; Barraud S; Bertherat J; Delemer B
    Endocrine; 2022 Oct; 78(1):201-204. PubMed ID: 35925470
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 37(7):1626-32. PubMed ID: 23592061
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Carney Complex Complicated with Primary Pigmented Nodular Adrenocortical Disease without Cushing's Syndrome Recurrence for Five Years after Unilateral Adrenalectomy.
    Tsurutani Y; Kiriyama K; Kondo M; Hasebe M; Sata A; Mizuno Y; Sugisawa C; Saito J; Nishikawa T
    Intern Med; 2022; 61(2):205-211. PubMed ID: 35034934
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hormonal, Radiological, NP-59 Scintigraphy, and Pathological Correlations in Patients With Cushing's Syndrome Due to Primary Pigmented Nodular Adrenocortical Disease (PPNAD).
    Vezzosi D; Tenenbaum F; Cazabat L; Tissier F; Bienvenu M; Carrasco CA; Laloi-Michelin M; Barrande G; Lefebvre H; Hiéronimus S; Tabarin A; Bertagna X; Legmann P; Vantyghem MC; Bertherat J
    J Clin Endocrinol Metab; 2015 Nov; 100(11):4332-8. PubMed ID: 26390100
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 13():913253. PubMed ID: 35992106
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Unilateral Adrenalectomy as a First-Line Treatment of Cushing's Syndrome in Patients With Primary Bilateral Macronodular Adrenal Hyperplasia.
    Debillon E; Velayoudom-Cephise FL; Salenave S; Caron P; Chaffanjon P; Wagner T; Massoutier M; Lambert B; Benoit M; Young J; Tabarin A; Chabre O
    J Clin Endocrinol Metab; 2015 Dec; 100(12):4417-24. PubMed ID: 26451908
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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; 128(9-10):268-73. PubMed ID: 17128664
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 59(9):823-30. PubMed ID: 22785148
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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. PubMed ID: 20924687
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Role of unilateral adrenalectomy in bilateral adrenal hyperplasias with Cushing's syndrome.
    Meloche-Dumas L; Mercier F; Lacroix A
    Best Pract Res Clin Endocrinol Metab; 2021 Mar; 35(2):101486. PubMed ID: 33637447
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Primary pigmented nodular adrenocortical dysplasia (PPNAD) within the scope of Carney complex as the etiology of Cushing syndrome].
    Koch CA; Bornstein SR; Chrousos GP; Stratakis CA
    Med Klin (Munich); 2000 Apr; 95(4):224-30. PubMed ID: 10808306
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 16(2):198-204. PubMed ID: 19833579
    [TBL] [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; 89(7):3173-82. PubMed ID: 15240590
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 9():277. PubMed ID: 26619967
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Carney Syndrome Presented as a Pathological Spine Fracture in a 35-Year-Old Male.
    Kiriakopoulos A; Linos D
    Am J Case Rep; 2018 Nov; 19():1366-1369. PubMed ID: 30442879
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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; 150(43):2390-3. PubMed ID: 17100132
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Carney complex with PRKAR1A gene mutation: A case report and literature review.
    Liu Q; Tong D; Liu G; Yi Y; Zhang D; Zhang J; Zhang Y; Huang Z; Li Y; Chen R; Guan Y; Yi X; Jiang J
    Medicine (Baltimore); 2017 Dec; 96(50):e8999. PubMed ID: 29390296
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A large family with Carney complex caused by the S147G PRKAR1A mutation shows a unique spectrum of disease including adrenocortical cancer.
    Anselmo J; Medeiros S; Carneiro V; Greene E; Levy I; Nesterova M; Lyssikatos C; Horvath A; Carney JA; Stratakis CA
    J Clin Endocrinol Metab; 2012 Feb; 97(2):351-9. PubMed ID: 22112814
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diurnal Plasma Cortisol Measurements Utility in Differentiating Various Etiologies of Endogenous Cushing Syndrome.
    Tirosh A; Lodish MB; Papadakis GZ; Lyssikatos C; Belyavskaya E; Stratakis CA
    Horm Metab Res; 2016 Sep; 48(10):677-681. PubMed ID: 27643448
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.