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Antoine Leenhardt
Researcher at Paris Diderot University
Publications - 20
Citations - 4067
Antoine Leenhardt is an academic researcher from Paris Diderot University. The author has contributed to research in topics: Catecholaminergic polymorphic ventricular tachycardia & Ventricular tachycardia. The author has an hindex of 15, co-authored 20 publications receiving 3514 citations. Previous affiliations of Antoine Leenhardt include French Institute of Health and Medical Research & University of Paris.
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HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.
Silvia G. Priori,Arthur A.M. Wilde,Minoru Horie,Yongkeun Cho,Elijah R. Behr,Charles I. Berul,Nico A. Blom,Josep Brugada,Chern En Chiang,Heikki V. Huikuri,Prince J. Kannankeril,Andrew D. Krahn,Antoine Leenhardt,Arthur J. Moss,Peter J. Schwartz,Wataru Shimizu,Gordon F. Tomaselli,Cynthia M. Tracy +17 more
TL;DR: Developed in partnership with the Heart Rhythm Society (HRS), the European Heart Rhythm Association (EHRA), a registered branch of the European Society of Cardiology, and the Asia Pacific Heart Rhythm society (APHRS).
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Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes
Silvia G. Priori,Arthur A.M. Wilde,Minoru Horie,Yongkeun Cho,Elijah R. Behr,Charles I. Berul,Nico A. Blom,Josep Brugada,Chern En Chiang,Heikki V. Huikuri,Prince J. Kannankeril,Andrew D. Krahn,Antoine Leenhardt,Arthur J. Moss,Peter J. Schwartz,Wataru Shimizu,Gordon F. Tomaselli,Cynthia M. Tracy,Michael J. Ackerman,Bernard Belhassen,N.A. Mark Estes,Diane Fatkin,Jonathan M. Kalman,Elizabeth S. Kaufman,Paulus Kirchhof,Eric Schulze-Bahr,Christian Wolpert,Jitendra K. Vohra,Marwan M. Refaat,Susan P. Etheridge,Robert M. Campbell,Edward T. Martin,Swee Chye Quek +32 more
TL;DR: This international consensus statement is the collaborative effort of three medical societies representing electrophysiology in North America, Europe, and Asian-Pacific area and summarizes the opinion of the international writing group members based on their own experience and on a general review of the literature.
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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Connie R. Bezzina,Julien Barc,Yuka Mizusawa,Carol Ann Remme,Jean-Baptiste Gourraud,Floriane Simonet,Floriane Simonet,Floriane Simonet,Arie O. Verkerk,Peter J. Schwartz,Lia Crotti,Federica Dagradi,Pascale Guicheney,Pascale Guicheney,Véronique Fressart,Véronique Fressart,Antoine Leenhardt,Antoine Leenhardt,Charles Antzelevitch,Susan Bartkowiak,Martin Borggrefe,Rainer Schimpf,Eric Schulze-Bahr,Sven Zumhagen,Elijah R. Behr,Rachel Bastiaenen,Jacob Tfelt-Hansen,Jacob Tfelt-Hansen,Morten S. Olesen,Morten S. Olesen,Stefan Kääb,Britt M. Beckmann,Peter Weeke,Hiroshi Watanabe,Naoto Endo,Tohru Minamino,Minoru Horie,Seiko Ohno,Kanae Hasegawa,Naomasa Makita,Akihiko Nogami,Wataru Shimizu,Takeshi Aiba,Philippe Froguel,Philippe Froguel,Philippe Froguel,Beverley Balkau,Beverley Balkau,Olivier Lantieri,Margherita Torchio,Cornelia Wiese,David Weber,Rianne Wolswinkel,Ruben Coronel,Bas J. Boukens,Stéphane Bézieau,Eric Charpentier,Eric Charpentier,Eric Charpentier,Stéphanie Chatel,Aurore Despres,Françoise Gros,Françoise Gros,Françoise Gros,Florence Kyndt,Simon Lecointe,Pierre Lindenbaum,Vincent Portero,Vincent Portero,Vincent Portero,Jade Violleau,Manfred Gessler,Hanno L. Tan,Dan M. Roden,Vincent M. Christoffels,Hervé Le Marec,Arthur A.M. Wilde,Vincent Probst,Jean-Jacques Schott,Christian Dina,Richard Redon +80 more
TL;DR: The association signals at SCN5A-SCN10A demonstrate that genetic polymorphisms modulating cardiac conduction can also influence susceptibility to cardiac arrhythmia and indicate that common genetic variation can have a strong impact on the predisposition to rare diseases.
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Absence of Triadin, a Protein of the Calcium Release Complex, is Responsible for Cardiac Arrhythmia with Sudden Death in Human
Nathalie Roux-Buisson,Marine Cacheux,Marine Cacheux,Anne Fourest-Lieuvin,Anne Fourest-Lieuvin,Jérémy Fauconnier,Julie Brocard,Julie Brocard,Isabelle Denjoy,Philippe Durand,Pascale Guicheney,Pascale Guicheney,Florence Kyndt,Antoine Leenhardt,Hervé Le Marec,Hervé Le Marec,V. Lucet,Philippe Mabo,Vincent Probst,Vincent Probst,Nicole Monnier,Pierre F. Ray,Pierre F. Ray,Elodie Santoni,Pauline Trémeaux,Alain Lacampagne,Julien Fauré,Julien Fauré,Joël Lunardi,Joël Lunardi,Isabelle Marty,Isabelle Marty +31 more
TL;DR: TRDN is identified as a new gene responsible for an autosomal recessive form of CPVT, and the mutations identified in the two families lead to the absence of the protein, thereby demonstrating the importance of triadin for the normal function of the cardiac calcium release complex in humans.
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Catecholaminergic Polymorphic Ventricular Tachycardia
TL;DR: In this paper, the authors used β-blockers without sympathomimetic activity to reduce the arrhythmic event rate in patients with Catecholaminergic polymorphic ventricular tachycardia.