These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

364 related items for PubMed ID: 28871709

  • 1. 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
    [Abstract] [Full Text] [Related]

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

  • 3. 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 Aug; 71():107632. PubMed ID: 38492686
    [Abstract] [Full Text] [Related]

  • 4. PRKAR1A in the development of cardiac myxoma: a study of 110 cases including isolated and syndromic tumors.
    Maleszewski JJ, Larsen BT, Kip NS, Castonguay MC, Edwards WD, Carney JA, Kipp BR.
    Am J Surg Pathol; 2014 Aug; 38(8):1079-87. PubMed ID: 24618615
    [Abstract] [Full Text] [Related]

  • 5. Case Report: An Atypical Case of Carney Complex.
    Khan Z, Alkhatib H, Ramani GV.
    Am J Case Rep; 2021 Oct 24; 22():e933744. PubMed ID: 34689149
    [Abstract] [Full Text] [Related]

  • 6. PRKAR1A mutation causing pituitary-dependent Cushing disease in a patient with Carney complex.
    Kiefer FW, Winhofer Y, Iacovazzo D, Korbonits M, Wolfsberger S, Knosp E, Trautinger F, Höftberger R, Krebs M, Luger A, Gessl A.
    Eur J Endocrinol; 2017 Aug 24; 177(2):K7-K12. PubMed ID: 28522647
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. A Novel Inherited Mutation in PRKAR1A Abrogates PreRNA Splicing in a Carney Complex Family.
    Sun Y, Chen X, Sun J, Wen X, Liu X, Zhang Y, Hoffman AR, Hu JF, Gao Y.
    Can J Cardiol; 2015 Nov 24; 31(11):1393-401. PubMed ID: 26416542
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. 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 27; 257(4):337-345. PubMed ID: 35732416
    [Abstract] [Full Text] [Related]

  • 12. Carney Syndrome Presented as a Pathological Spine Fracture in a 35-Year-Old Male.
    Kiriakopoulos A, Linos D.
    Am J Case Rep; 2018 Nov 16; 19():1366-1369. PubMed ID: 30442879
    [Abstract] [Full Text] [Related]

  • 13. Unusual Findings in a Patient With Carney Complex due to a Novel PRKAR1A Mutation.
    Friedrich RE, Zenker M.
    Anticancer Res; 2022 Dec 16; 42(12):6121-6125. PubMed ID: 36456122
    [Abstract] [Full Text] [Related]

  • 14. Diagnosis and cardiac transplantation of a Carney syndrome-induced cardiac myxoma combined with dilated cardiomyopathy: a case report.
    Cheng C, Song Y, Yan H, Bao D, Zhang X, Zhao Y, Liu D, Zhang D.
    BMC Cardiovasc Disord; 2024 Jun 17; 24(1):307. PubMed ID: 38886700
    [Abstract] [Full Text] [Related]

  • 15. 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 17; 96(1):E208-14. PubMed ID: 21047926
    [Abstract] [Full Text] [Related]

  • 16. 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 27; 13():83. PubMed ID: 25890363
    [Abstract] [Full Text] [Related]

  • 17. Liver findings in patients with Carney complex, germline PRKAR1A pathogenic variants, and link to cardiac myxomas.
    Tirosh A, Hamimi A, Faucz F, Aharon-Hananel G, Zavras PD, Bonella B, Auerbach A, Gillis D, Lyssikatos C, Belyavskaya E, Stratakis CA, Gharib AM.
    Endocr Relat Cancer; 2020 Jun 27; 27(6):355-360. PubMed ID: 32302974
    [Abstract] [Full Text] [Related]

  • 18. 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 27; 168(11):1401-4. PubMed ID: 19219454
    [Abstract] [Full Text] [Related]

  • 19. Acromegaly in Carney complex.
    Cuny T, Mac TT, Romanet P, Dufour H, Morange I, Albarel F, Lagarde A, Castinetti F, Graillon T, North MO, Barlier A, Brue T.
    Pituitary; 2019 Oct 27; 22(5):456-466. PubMed ID: 31264077
    [Abstract] [Full Text] [Related]

  • 20. PRKAR1A mutations in primary pigmented nodular adrenocortical disease.
    Cazabat L, Ragazzon B, Groussin L, Bertherat J.
    Pituitary; 2006 Oct 27; 9(3):211-9. PubMed ID: 17036196
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 19.