Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Philippe Charron

Showing results (51-60 of 203) with videos related to

Pageof 21
Sort By:
International Journal of Cardiology|July 17, 2012
Expanding the phenotype associated with a desmoplakin dominant mutation: Carvajal/Naxos syndrome associated with leukonychia and oligodontiaStéphane Boulé, Veronique Fressart, Daniela Laux, et al.
Microorganisms|November 27, 2024
How Gut Microbiome Perturbation Caused by Antibiotic Pre-Treatments Affected the Conjugative Transfer of Antimicrobial Resistance GenesGokhan Yilmaz, Maria Chan, Calvin Ho-Fung Lau, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|September 4, 2025
A Nationwide Study of the Economic Burden of Obstructive Hypertrophic Cardiomyopathy in FrancePhilippe Charron, Carla Zema, François-Emery Cotté, et al.
Heart Rhythm|June 14, 2025
Prognosis for loss-of-function versus hot-spot variants in RBM20-related cardiomyopathyAlexis Hermida, Flavie Ader, Guillaume Jedraszak, et al.
Archives of Cardiovascular Diseases|August 11, 2020
The value of electrocardiography and echocardiography in distinguishing Fabry disease from sarcomeric hypertrophic cardiomyopathyNicolas Junqua, Damien Legallois, Sophie Segard, 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|July 17, 2013
Screening of genes encoding junctional candidates in arrhythmogenic right ventricular cardiomyopathy/dysplasiaEstelle Gandjbakhch, Alexia Vite, Françoise Gary, et al.
Journal of Cardiovascular Electrophysiology|December 18, 2007
Brugada syndrome in pure black AfricansAimé Bonny, Joelci Tonet, Guy Fontaine, 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|December 18, 2019
Desmoglein-2 mutations in propeptide cleavage-site causes arrhythmogenic right ventricular cardiomyopathy/dysplasia by impairing extracellular 1-dependent desmosomal interactions upon cellular stressAlexia Vite, Estelle Gandjbakhch, Tiphaine Hery, et al.
Journal of Clinical Medicine|June 12, 2026
Use of Disopyramide in Obstructive Hypertrophic Cardiomyopathy: A European InsightPhilippe Charron, Faizel Osman, Jean-Noel Trochu, et al.
Medicine|August 13, 2015
Reversible Severe Eosinophilic Endomyocardial Fibrosis During Pregnancy: A Case ReportMarc Pineton de Chambrun, Philippe Charron, Danièle Vauthier-Brouzes, et al.
Pageof 21

Showing results (51-60 of 203) with videos related to

Sort By:
Pageof 21
International Journal of Cardiology|July 17, 2012
Expanding the phenotype associated with a desmoplakin dominant mutation: Carvajal/Naxos syndrome associated with leukonychia and oligodontiaStéphane Boulé, Veronique Fressart, Daniela Laux, et al.
Microorganisms|November 27, 2024
How Gut Microbiome Perturbation Caused by Antibiotic Pre-Treatments Affected the Conjugative Transfer of Antimicrobial Resistance GenesGokhan Yilmaz, Maria Chan, Calvin Ho-Fung Lau, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|September 4, 2025
A Nationwide Study of the Economic Burden of Obstructive Hypertrophic Cardiomyopathy in FrancePhilippe Charron, Carla Zema, François-Emery Cotté, et al.
Heart Rhythm|June 14, 2025
Prognosis for loss-of-function versus hot-spot variants in RBM20-related cardiomyopathyAlexis Hermida, Flavie Ader, Guillaume Jedraszak, et al.
Archives of Cardiovascular Diseases|August 11, 2020
The value of electrocardiography and echocardiography in distinguishing Fabry disease from sarcomeric hypertrophic cardiomyopathyNicolas Junqua, Damien Legallois, Sophie Segard, 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|July 17, 2013
Screening of genes encoding junctional candidates in arrhythmogenic right ventricular cardiomyopathy/dysplasiaEstelle Gandjbakhch, Alexia Vite, Françoise Gary, et al.
Journal of Cardiovascular Electrophysiology|December 18, 2007
Brugada syndrome in pure black AfricansAimé Bonny, Joelci Tonet, Guy Fontaine, 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|December 18, 2019
Desmoglein-2 mutations in propeptide cleavage-site causes arrhythmogenic right ventricular cardiomyopathy/dysplasia by impairing extracellular 1-dependent desmosomal interactions upon cellular stressAlexia Vite, Estelle Gandjbakhch, Tiphaine Hery, et al.
Journal of Clinical Medicine|June 12, 2026
Use of Disopyramide in Obstructive Hypertrophic Cardiomyopathy: A European InsightPhilippe Charron, Faizel Osman, Jean-Noel Trochu, et al.
Medicine|August 13, 2015
Reversible Severe Eosinophilic Endomyocardial Fibrosis During Pregnancy: A Case ReportMarc Pineton de Chambrun, Philippe Charron, Danièle Vauthier-Brouzes, et al.
Pageof 21