Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Eric Rendu"'
Autor:
Jean-Pierre Camous, Stéphane Bézieau, Philippe Maury, Michel Haïssaguerre, Jacques Mansourati, Guillaume Tournant, Eric Delannoy, Isabelle Magnin, Hervé Le Marec, Véronique Fressart, Philippe Mabo, Florence Kyndt, Vincent Probst, Frederic Sacher, Béatrice Guyomarch, Eric Rendu, Isabelle Denjoy
Publikováno v:
Europace. 15:1805-1811
Aims Andersen–Tawil syndrome (ATS) is an uncommon form of channelopathy linked to mutations in the KCNJ2 gene. Currently, little is known about the long-term arrhythmic prognosis of this disease. Methods and results We conducted a retrospective mul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f25dd1f2c435e0f8f6f2ab30ecfb3dab
https://doi.org/10.1093/europace/eut160
https://doi.org/10.1093/europace/eut160
Autor:
Karim Gacem, Florence Kyndt, Vincent Probst, Estelle Baron, Jean-Jacques Schott, Swanny Fouchard, Jean Marc Dupuis, Stéphanie Chatel, Jean-Pierre Cebron, Aurelie Longueville, Hervé Le Marec, Matilde Karakachoff, Philippe Jaafar, Claude Gully, Jean-Baptiste Gourraud, Eric Rendu
Publikováno v:
Heart
Heart, 2012, 98 (17), pp.1305-1310. ⟨10.1136/heartjnl-2012-301872⟩
Heart, BMJ Publishing Group, 2012, 98 (17), pp.1305-1310. ⟨10.1136/heartjnl-2012-301872⟩
Heart, 2012, 98 (17), pp.1305-1310. ⟨10.1136/heartjnl-2012-301872⟩
Heart, BMJ Publishing Group, 2012, 98 (17), pp.1305-1310. ⟨10.1136/heartjnl-2012-301872⟩
International audience; INTRODUCTION:Progressive cardiac conduction defect (PCCD) is a frequent disease attributed to degeneration and fibrosis of the His bundle. Over the past years, gene defects have been identified demonstrating that PCCD could be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::205dbbdfd226753a686a0634a604c03e
https://www.hal.inserm.fr/inserm-01667205
https://www.hal.inserm.fr/inserm-01667205
