Progressive Cardiac Conduction Defect is the Prevailing Phenotype in Carriers of a Brugada Syndrome <i>SCN5A</i> MutationVincent Probst, Hervé Le Marec, Marie Allouis et al.|Journal of Cardiovascular Electrophysiology|2006Cited by 115
14-3-3 Is a Regulator of the Cardiac Voltage-Gated Sodium Channel Nav1.5Marie Allouis, Isabelle Baró, Françoise Le Bouffant et al.|Circulation Research|2006Cited by 90
Monomorphic Ventricular Tachycardia Due to Brugada Syndrome Successfully Treated by Hydroquinidine Therapy in a 3‐Year‐Old ChildVincent Probst, Hervé Le Marec, Stéphane Evain et al.|Journal of Cardiovascular Electrophysiology|2005Cited by 50
Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutationMarie Allouis, Hervé Le Marec, Vincent Probst et al.|The American Journal of Cardiology|2005Cited by 25
[Genetic aspects of cardiac conduction defects].Vincent Probst, Hervé Le Marec, Florence Kyndt et al.|PubMed|2003Cited by 4