Publicaciones en colaboración con investigadores/as de Universidade da Coruña (6)

2021

  1. Association of Left Ventricular Systolic Dysfunction among Carriers of Truncating Variants in Filamin C with Frequent Ventricular Arrhythmia and End-stage Heart Failure

    JAMA Cardiology, Vol. 6, Núm. 8, pp. 891-901

  2. Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry

    Revista Espanola de Cardiologia, Vol. 74, Núm. 3, pp. 216-224

  3. Selection of the best of 2020 in familial heart disease and cardiovascular genetics

    REC: CardioClinics, Vol. 56, pp. 9-14

2018

  1. Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations

    Journal of the American College of Cardiology, Vol. 72, Núm. 20, pp. 2471-2481

2016

  1. Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies

    Journal of the American College of Cardiology, Vol. 68, Núm. 22, pp. 2440-2451

2013

  1. Functional characterization of a novel frameshift mutation in the c-terminus of the nav1.5 channel underlying a brugada syndrome with variable expression in a spanish family

    PLoS ONE, Vol. 8, Núm. 11