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Journal of Cardiovascular Electrophysiology|March 19, 2025
Endo-Epicardial vs. Endocardial-Only Catheter Ablation of Ventricular Tachycardia in Patients With Ischemic Cardiomyopathy: The EPIC-VT Trial DesignRaphaël P Martins, Pierre Groussin, Francis Bessière, et al.
Heart Rhythm|April 16, 2017
The QUIDAM study: Hydroquinidine therapy for the management of Brugada syndrome patients at high arrhythmic riskAntoine Andorin, Jean-Baptiste Gourraud, Jacques Mansourati, et al.
The American Journal of Cardiology|September 10, 2013
Prevalence and prognostic role of various conduction disturbances in patients with the Brugada syndromePhilippe Maury, Anne Rollin, Frédéric Sacher, et al.
European Heart Journal|December 13, 2016
Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1Karim Wahbi, Dominique Babuty, Vincent Probst, et al.
European Heart Journal|December 8, 2020
Robustness and relevance of predictive score in sudden cardiac death for patients with Brugada syndromeVincent Probst, Thomas Goronflot, Soraya Anys, et al.
Heart Rhythm|July 2, 2017
Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivityDylan Therasse, Frederic Sacher, Bertrand Petit, et al.
Cardiovascular Research|September 8, 2020
Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conductionZeina R Al Sayed, Robin Canac, Bastien Cimarosti, et al.
Heart Rhythm|July 26, 2015
Increased Tpeak-Tend interval is highly and independently related to arrhythmic events in Brugada syndromePhilippe Maury, Frederic Sacher, Jean-Baptiste Gourraud, et al.
International Journal of Cardiology|January 29, 2016
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type IXavier Daumy, Mohamed-Yassine Amarouch, Pierre Lindenbaum, et al.
Basic Research in Cardiology|October 25, 2014
Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutationsDelphine M Béziau, Julien Barc, Thomas O'Hara, et al.
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