Publicacións en colaboración con investigadores/as de Masonic Medical Research Laboratory (5)

2012

  1. A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Nav1.5 and Kv4.3 channel currents

    Heart Rhythm, Vol. 9, Núm. 5, pp. 760-769

  2. Maximum diastolic potential of human induced pluripotent stem cell-derived cardiomyocytes depends critically on IKr

    PLoS ONE, Vol. 7, Núm. 7

  3. Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8

    Heart Rhythm, Vol. 9, Núm. 4, pp. 548-555

2011

  1. LQT5 masquerading as LQT2: A dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current

    Europace, Vol. 13, Núm. 10, pp. 1478-1483

2007

  1. Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

    Circulation, Vol. 115, Núm. 4, pp. 442-449