Works matching IS 20358253 AND DT 2019 AND VI 9 AND IP 1

Results: 6
    1
    2

    FLNC missense variants in familial noncompaction cardiomyopathy.

    Published in:
    Cardiogenetics, 2019, v. 9, n. 1, p. 9, doi. 10.4081/cardiogenetics.2019.8181
    By:
    • van Waning, Jaap I.;
    • Hoedemaekers, Yvonne M.;
    • te Rijdt, Wouter P.;
    • Jpma, Arne I.;
    • Heijsman, Daphne;
    • Caliskan, Kadir;
    • Hoendermis, Elke S.;
    • Willems, Tineke P.;
    • van den Wijngaard, Arthur;
    • Suurmeijer, Albert;
    • van Slegtenhorst, Marjon A.;
    • Jongbloed, Jan D. H.;
    • Majoor-Krakauer, Danielle F.;
    • van der Zwaag, Paul A.
    Publication type:
    Article
    3
    4
    5

    Atrial myxoma and Williams-Beuren syndrome. An incidental association?

    Published in:
    Cardiogenetics, 2019, v. 9, n. 1, p. 3, doi. 10.4081/cardiogenetics.2019.7779
    By:
    • Limongelli, Giuseppe;
    • Fratta, Fiorella;
    • Cirillo, Annapaola;
    • Fusco, Adelaide;
    • Marrazzo, Tommaso;
    • Tramonte, Stefania;
    • Caiazza, Martina;
    • Caianiello, Giuseppe;
    • Russo, Maria Giovanna
    Publication type:
    Article
    6

    An unusual cause of right heart failure.

    Published in:
    Cardiogenetics, 2019, v. 9, n. 1, p. 4, doi. 10.4081/cardiogenetics.2019.7503
    By:
    • Hill, Paul;
    • Sidhu, Jagdip;
    • Bastiaenen, Rachel
    Publication type:
    Article