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Philippe Charron

Showing results (91-100 of 203) with videos related to

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Open Medicine (Warsaw, Poland)|December 18, 2020
Clinical impact of post-mortem genetic testing in cardiac death and cardiomyopathyIsabelle Marey, Véronique Fressart, Caroline Rambaud, et al.
Plos One|October 3, 2013
Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient heartsAlexia Vite, Estelle Gandjbakhch, Catherine Prost, et al.
European Heart Journal|December 6, 2012
Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial DiseasesClaudio Rapezzi, Eloisa Arbustini, Alida L P Caforio, 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|September 5, 2025
Family history of sudden cardiac death as a risk marker for ventricular arrhythmias in laminopathiesGauthier Giordano, Julie Proukhnitzky, Frédéric Fer, et al.
Archives of Cardiovascular Diseases|February 6, 2022
Prevalence of familial hypercholesterolaemia in patients presenting with premature acute coronary syndromeMarie Hauguel-Moreau, Vincent Aïdan, Hélène Hergault, et al.
Kardiologia Polska|July 18, 2008
[Classification of the cardiomyopathies]Perry Elliott, Bert Andersson, Eloisa Arbustini, et al.
European Heart Journal|October 6, 2007
Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial DiseasesPerry Elliott, Bert Andersson, Eloisa Arbustini, et al.
Heart (British Cardiac Society)|July 28, 2019
Mid-regional proatrial natriuretic peptide for predicting prognosis in hypertrophic cardiomyopathyCéline Bégué, Stellan Mörner, Dulce Brito, et al.
Circulation|April 23, 2003
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategyPascale Richard, Philippe Charron, Lucie Carrier, et al.
JACC. Heart Failure|September 25, 2025
Pathophysiology and Therapeutic Needs in Nonobstructive Hypertrophic CardiomyopathyMilind Y Desai, Niccolo Maurizi, Elena Biagini, et al.
Pageof 21

Showing results (91-100 of 203) with videos related to

Sort By:
Pageof 21
Open Medicine (Warsaw, Poland)|December 18, 2020
Clinical impact of post-mortem genetic testing in cardiac death and cardiomyopathyIsabelle Marey, Véronique Fressart, Caroline Rambaud, et al.
Plos One|October 3, 2013
Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient heartsAlexia Vite, Estelle Gandjbakhch, Catherine Prost, et al.
European Heart Journal|December 6, 2012
Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial DiseasesClaudio Rapezzi, Eloisa Arbustini, Alida L P Caforio, 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|September 5, 2025
Family history of sudden cardiac death as a risk marker for ventricular arrhythmias in laminopathiesGauthier Giordano, Julie Proukhnitzky, Frédéric Fer, et al.
Archives of Cardiovascular Diseases|February 6, 2022
Prevalence of familial hypercholesterolaemia in patients presenting with premature acute coronary syndromeMarie Hauguel-Moreau, Vincent Aïdan, Hélène Hergault, et al.
Kardiologia Polska|July 18, 2008
[Classification of the cardiomyopathies]Perry Elliott, Bert Andersson, Eloisa Arbustini, et al.
European Heart Journal|October 6, 2007
Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial DiseasesPerry Elliott, Bert Andersson, Eloisa Arbustini, et al.
Heart (British Cardiac Society)|July 28, 2019
Mid-regional proatrial natriuretic peptide for predicting prognosis in hypertrophic cardiomyopathyCéline Bégué, Stellan Mörner, Dulce Brito, et al.
Circulation|April 23, 2003
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategyPascale Richard, Philippe Charron, Lucie Carrier, et al.
JACC. Heart Failure|September 25, 2025
Pathophysiology and Therapeutic Needs in Nonobstructive Hypertrophic CardiomyopathyMilind Y Desai, Niccolo Maurizi, Elena Biagini, et al.
Pageof 21