BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

232 related articles for article (PubMed ID: 20850710)

  • 1. Carney complex: Clinical and genetic 2010 update.
    Vezzosi D; Vignaux O; Dupin N; Bertherat J
    Ann Endocrinol (Paris); 2010 Dec; 71(6):486-93. PubMed ID: 20850710
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Carney complex.
    Espiard S; Bertherat J
    Front Horm Res; 2013; 41():50-62. PubMed ID: 23652670
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Case studies of two related Chinese patients with Carney complex presenting with extensive cardiac myxomas and PRKAR1A gene mutation of c.491_492delTG.
    Guo H; Xu J; Xiong H; Hu S
    World J Surg Oncol; 2015 Feb; 13():83. PubMed ID: 25890363
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel PRKAR1A gene mutations in Carney Complex.
    Pan L; Peng L; Jean-Gilles J; Zhang X; Wieczorek R; Jain S; Levine V; Osman I; Prieto VG; Lee P
    Int J Clin Exp Pathol; 2010 May; 3(5):545-8. PubMed ID: 20606737
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Carney complex].
    Losada Grande EJ; Al Kassam Martínez D; González Boillos M
    Endocrinol Nutr; 2011; 58(6):308-14. PubMed ID: 21536508
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Carney complex: an update.
    Correa R; Salpea P; Stratakis CA
    Eur J Endocrinol; 2015 Oct; 173(4):M85-97. PubMed ID: 26130139
    [TBL] [Abstract][Full Text] [Related]  

  • 7. MANAGEMENT OF ENDOCRINE DISEASE: Carney complex: clinical and genetic update 20 years after the identification of the CNC1 (PRKAR1A) gene.
    Bouys L; Bertherat J
    Eur J Endocrinol; 2021 Mar; 184(3):R99-R109. PubMed ID: 33444222
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unusual presentations of Carney Complex in patient with a novel PRKAR1A mutation.
    Akin S; Noyan S; Dagdelen S; Pasaoglu I; Kaynaroglu V; Askun MM; Bilen CY; Kiratli H; Baydar DE; Onder S; Sokmensuer C; Aytemir K; Erkin G; Kiratli PO; Alikasifoglu M; Erbas T
    Neuro Endocrinol Lett; 2017 Aug; 38(4):248-254. PubMed ID: 28871709
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Carney Complex.
    Kamilaris CDC; Faucz FR; Voutetakis A; Stratakis CA
    Exp Clin Endocrinol Diabetes; 2019 Feb; 127(2-03):156-164. PubMed ID: 30428497
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Psammomatous melanotic schwannoma as indicator of a Carney complex].
    Seidl M; Zolnhofer G; Gunser S; Ennker J; Schäfer W; Tietze L
    Pathologe; 2013 Jul; 34(4):343-6. PubMed ID: 23306533
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome.
    Sahut-Barnola I; Lefrançois-Martinez AM; Dufour D; Botto JM; Kamilaris C; Faucz FR; Stratakis CA; Val P; Martinez A
    J Invest Dermatol; 2022 Nov; 142(11):2949-2957.e9. PubMed ID: 35568059
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype.
    Libé R; Horvath A; Vezzosi D; Fratticci A; Coste J; Perlemoine K; Ragazzon B; Guillaud-Bataille M; Groussin L; Clauser E; Raffin-Sanson ML; Siegel J; Moran J; Drori-Herishanu L; Faucz FR; Lodish M; Nesterova M; Bertagna X; Bertherat J; Stratakis CA
    J Clin Endocrinol Metab; 2011 Jan; 96(1):E208-14. PubMed ID: 21047926
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenotypic Variability in a Family with Carney Complex Accompanied by a Novel Mutation Involving PRKAR1A.
    Kubo H; Tsurutani Y; Sugisawa C; Sunouchi T; Hirose R; Saito J
    Tohoku J Exp Med; 2022 Jul; 257(4):337-345. PubMed ID: 35732416
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frequent protein kinase A regulatory subunit A1 mutations but no GNAS mutations as potential driver in sporadic cardiac myxomas.
    Zimpfer A; Abel LM; Alozie A; Etz CD; Schneider B
    Cardiovasc Pathol; 2024; 71():107632. PubMed ID: 38492686
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and molecular genetics of Carney complex.
    Rothenbuhler A; Stratakis CA
    Best Pract Res Clin Endocrinol Metab; 2010 Jun; 24(3):389-99. PubMed ID: 20833331
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recurrent left atrial myxomas in Carney complex: a genetic cause of multiple strokes that can be prevented.
    Briassoulis G; Kuburovic V; Xekouki P; Patronas N; Keil MF; Lyssikatos C; Stajevic M; Kovacevic G; Stratakis CA
    J Stroke Cerebrovasc Dis; 2012 Nov; 21(8):914.e1-8. PubMed ID: 22341669
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Carney complex 1 with PRKAR1A mutations manifesting as multiple repeated skin myxomas: A case report.
    Sakugawa H; Hayashi K; Uema M; Miyagi T; Utsumi D; Yamaguchi S; Takahashi K
    J Dermatol; 2020 Apr; 47(4):e122-e124. PubMed ID: 32011755
    [No Abstract]   [Full Text] [Related]  

  • 18. Familial recurrent atrial myxoma: Carney's complex.
    Shetty Roy AN; Radin M; Sarabi D; Shaoulian E
    Clin Cardiol; 2011 Feb; 34(2):83-6. PubMed ID: 21298650
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cutaneous signs are important in the diagnosis of the rare neoplasia syndrome Carney complex.
    Vandersteen A; Turnbull J; Jan W; Simpson J; Lucas S; Anderson D; Lin JP; Stratakis C; Pichert G; Lim M
    Eur J Pediatr; 2009 Nov; 168(11):1401-4. PubMed ID: 19219454
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carney complex due to a novel pathogenic variant in the PRKAR1A gene - a case report.
    Ferreira SH; Costa MM; Rios E; Santos Silva R; Costa C; Castro-Correia C; Fontoura M
    J Pediatr Endocrinol Metab; 2019 Feb; 32(2):197-202. PubMed ID: 30699069
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.