V
Vincent Probst
Researcher at University of Nantes
Publications - 237
Citations - 17375
Vincent Probst is an academic researcher from University of Nantes. The author has contributed to research in topics: Brugada syndrome & Sudden death. The author has an hindex of 55, co-authored 210 publications receiving 14699 citations. Previous affiliations of Vincent Probst include French Institute of Health and Medical Research & Centre national de la recherche scientifique.
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Journal ArticleDOI
Sudden Cardiac Arrest Associated with Early Repolarization
Michel Haïssaguerre,Nicolas Derval,Frederic Sacher,Laurence Jesel,Isabel Deisenhofer,Luc De Roy,Jean-Luc Pasquié,Akihiko Nogami,Dominique Babuty,Sinikka Yli-Mäyry,Christian de Chillou,Patrice Scanu,Philippe Mabo,Seiichiro Matsuo,Vincent Probst,Solena Le Scouarnec,Pascal Defaye,Juerg Schlaepfer,Thomas Rostock,Dominique Lacroix,Dominique Lamaison,Thomas Lavergne,Yoshifusa Aizawa,Anders Englund,Frédéric Anselme,Mark D O'Neill,Mélèze Hocini,Kang-Teng Lim,Sébastien Knecht,George D. Veenhuyzen,Pierre Bordachar,Michel Chauvin,Pierre Jaïs,Gaelle Coureau,Geneviève Chêne,George Klein,Jacques Clémenty +36 more
TL;DR: Among patients with a history of idiopathic ventricular fibrillation, there is an increased prevalence of early repolarization and during a mean (+/-SD) follow-up of 61+/-50 months, defibrillator monitoring showed a higher incidence of recurrent ventricularfibrillation in case subjects with a repolarized abnormality than in those without such an abnormality.
Journal ArticleDOI
2018 ESC Guidelines for the diagnosis and management of syncope.
Michele Brignole,Angel Moya,Frederik J. de Lange,Jean-Claude Deharo,Perry M. Elliott,Alessandra Fanciulli,Artur Fedorowski,Raffaello Furlan,Rose Anne Kenny,Alfonso Martín,Vincent Probst,Matthew J. Reed,Ciara Rice,Richard Sutton,Andrea Ungar,J. Gert van Dijk +15 more
TL;DR: Authors/Task Force Members: Michele Brignole* (Chairperson), Angel Moya* (Co-chairperson) (Spain), Frederik J. de Lange (The Netherlands), Jean-Claude Deharo (France), Perry M. Elliott (UK), Alessandra Fanciulli (Austria), Artur Fedorowski (Sweden), Raffaello Furlan (Italy), Rose Anne Kenny (Ireland), Alfonso Mart ın (Spain
Journal ArticleDOI
Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome Results From the FINGER Brugada Syndrome Registry
Vincent Probst,Christian Veltmann,Lars Eckardt,Paola G. Meregalli,Fiorenzo Gaita,Hanno L. Tan,Dominique Babuty,Frederic Sacher,Carla Giustetto,Eric Schulze-Bahr,Martin Borggrefe,M. Haissaguerre,Philippe Mabo,H. Le Marec,Christian Wolpert,Arthur A.M. Wilde +15 more
TL;DR: In the largest series of Brugada syndrome patients thus far, event rates in asymptomatic patients were low and gender, familial history of SCD, inducibility of ventricular tachyarrhythmias during electrophysiological study, and the presence of an SCN5A mutation were not predictive of arrhythmic events.
Journal ArticleDOI
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.
Jamie D. Kapplinger,David J. Tester,Marielle Alders,Begoña Benito,Myriam Berthet,Josep Brugada,Pedro Brugada,Véronique Fressart,Alejandra Guerchicoff,Carole Harris-Kerr,Shiro Kamakura,Florence Kyndt,Florence Kyndt,Tamara T. Koopmann,Yoshihiro Miyamoto,Ryan Pfeiffer,Guido D. Pollevick,Vincent Probst,Sven Zumhagen,Matteo Vatta,Jeffrey A. Towbin,Wataru Shimizu,Eric Schulze-Bahr,Charles Antzelevitch,Benjamin A. Salisbury,Pascale Guicheney,Arthur A.M. Wilde,Ramon Brugada,Jean-Jacques Schott,Jean-Jacques Schott,Jean-Jacques Schott,Michael J. Ackerman +31 more
TL;DR: Overall, 21% of BrS probands have mutations in SCN5A compared to the 2% to 5% background rate of rare variants reported in healthy control subjects, which may help further distinguish pathogenic mutations from similarly rare but otherwise innocuous ones found in cases.