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Philippe Charron

Showing results (21-30 of 203) with videos related to

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Medecine Sciences : M/S|November 13, 2018
[Genotype-phenotype correlations of pathogenic variants in the FLNC gene]Flavie Ader, Eric Villard, Céline Ledeuil, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|May 8, 2007
A familial form of conduction defect related to a mutation in the PRKAG2 genePhilippe Charron, Marc Genest, Pascale Richard, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|January 26, 2016
What's new in 2015 ESC guidelines on pericardial diseases?Massimo Imazio, Antonio Brucato, Luigi Badano, et al.
European Heart Journal|March 8, 2022
European Reference Network for rare, low prevalence, or complex diseases of the heart (ERN GUARD-Heart): 5 year anniversaryAhmad S Amin, Ruth Biller, Philippe Charron, et al.
Heartrhythm Case Reports|May 12, 2017
Recurrent suspected myocarditis combined with infrahisian conduction disturbances revealing a desminopathyStéphane Boulé, Pascale Richard, Pascal de Groote, et al.
Presse Medicale (Paris, France : 1983)|May 29, 2016
[Risk stratification of sudden death in hypertrophic cardiomyopathy in 2016]Olivier Dubourg, Philippe Charron, Marc Sirol, et al.
Biochemical and Biophysical Research Communications|January 24, 2012
Structures of the lamin A/C R335W and E347K mutants: implications for dilated cardiolaminopathiesMichela Bollati, Alberto Barbiroli, Valentina Favalli, et al.
British Journal of Sports Medicine|October 26, 2012
Advising a cardiac disease gene positive yet phenotype negative or borderline abnormal athlete: is sporting disqualification really necessary?Pascale Richard, Isabelle Denjoy, Véronique Fressart, et al.
Revista Espanola De Cardiologia (English Ed.)|May 11, 2025
Systematic triplet expansion testing in patients with genetically negative Brugada syndromeAlexis Hermida, Guillaume Jedraszak, Flavie Ader, et al.
Cardiovascular Research|June 6, 2009
A potential link between peroxisome proliferator-activated receptor signalling and the pathogenesis of arrhythmogenic right ventricular cardiomyopathyFatima Djouadi, Yves Lecarpentier, Jean-Louis Hébert, et al.
Pageof 21

Showing results (21-30 of 203) with videos related to

Sort By:
Pageof 21
Medecine Sciences : M/S|November 13, 2018
[Genotype-phenotype correlations of pathogenic variants in the FLNC gene]Flavie Ader, Eric Villard, Céline Ledeuil, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|May 8, 2007
A familial form of conduction defect related to a mutation in the PRKAG2 genePhilippe Charron, Marc Genest, Pascale Richard, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|January 26, 2016
What's new in 2015 ESC guidelines on pericardial diseases?Massimo Imazio, Antonio Brucato, Luigi Badano, et al.
European Heart Journal|March 8, 2022
European Reference Network for rare, low prevalence, or complex diseases of the heart (ERN GUARD-Heart): 5 year anniversaryAhmad S Amin, Ruth Biller, Philippe Charron, et al.
Heartrhythm Case Reports|May 12, 2017
Recurrent suspected myocarditis combined with infrahisian conduction disturbances revealing a desminopathyStéphane Boulé, Pascale Richard, Pascal de Groote, et al.
Presse Medicale (Paris, France : 1983)|May 29, 2016
[Risk stratification of sudden death in hypertrophic cardiomyopathy in 2016]Olivier Dubourg, Philippe Charron, Marc Sirol, et al.
Biochemical and Biophysical Research Communications|January 24, 2012
Structures of the lamin A/C R335W and E347K mutants: implications for dilated cardiolaminopathiesMichela Bollati, Alberto Barbiroli, Valentina Favalli, et al.
British Journal of Sports Medicine|October 26, 2012
Advising a cardiac disease gene positive yet phenotype negative or borderline abnormal athlete: is sporting disqualification really necessary?Pascale Richard, Isabelle Denjoy, Véronique Fressart, et al.
Revista Espanola De Cardiologia (English Ed.)|May 11, 2025
Systematic triplet expansion testing in patients with genetically negative Brugada syndromeAlexis Hermida, Guillaume Jedraszak, Flavie Ader, et al.
Cardiovascular Research|June 6, 2009
A potential link between peroxisome proliferator-activated receptor signalling and the pathogenesis of arrhythmogenic right ventricular cardiomyopathyFatima Djouadi, Yves Lecarpentier, Jean-Louis Hébert, et al.
Pageof 21