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Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|July 23, 2013
Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutationEric Delannoy, Frédéric Sacher, Philippe Maury, et al.
Heart Rhythm|September 9, 2018
Clinical presentation and follow-up of women affected by Brugada syndromePauline Berthome, Romain Tixier, Jean Briand, et al.
European Journal of Heart Failure|February 22, 2019
High risk of heart failure associated with desmoglein-2 mutations compared to plakophilin-2 mutations in arrhythmogenic right ventricular cardiomyopathy/dysplasiaAlexis Hermida, Véronique Fressart, Francoise Hidden-Lucet, et al.
Clinical and Translational Medicine|November 29, 2021
A standardised hERG phenotyping pipeline to evaluate KCNH2 genetic variant pathogenicityBarbara Oliveira-Mendes, Sylvain Feliciangeli, Mélissa Ménard, et al.
Heart (British Cardiac Society)|June 22, 2012
Identification of a strong genetic background for progressive cardiac conduction defect by epidemiological approachJean Baptiste Gourraud, Florence Kyndt, Swanny Fouchard, et al.
Cardiac Electrophysiology Clinics|August 4, 2017
Early Repolarization DiseaseAshok J Shah, Frédéric Sacher, Stéphanie Chatel, et al.
Stem Cell Research|January 9, 2022
Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic backgroundAurore Girardeau, Diane Atticus, Robin Canac, et al.
Heart Rhythm|March 3, 2009
Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathiesPaola G Meregalli, Hanno L Tan, Vincent Probst, et al.
Heart Rhythm|December 3, 2019
Age at diagnosis of Brugada syndrome: Influence on clinical characteristics and risk of arrhythmiaMathilde Minier, Vincent Probst, Pauline Berthome, et al.
Circulation|December 28, 2006
Mutations in the gene encoding filamin A as a cause for familial cardiac valvular dystrophyFlorence Kyndt, Jean-Pierre Gueffet, Vincent Probst, et al.
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