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Philippe Charron

Showing results (71-80 of 203) with videos related to

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Microbiology Spectrum|March 26, 2026
Two novel real-time PCR assays for <i>Brucella</i> detection: a species-specific multiplex and a genus-level singleplex developed via large-scale whole genome sequencing data analysisEmily Hoover, John Chmara, Marc-Olivier Duceppe, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|May 27, 2021
Hypertrophic cardiomyopathies requiring more monitoring for less atrial fibrillation-related complications: a clustering analysis based on the French registry on hypertrophic cardiomyopathy (REMY)Marion Hourqueig, Guillaume Bouzille, Mariana Mirabel, et al.
Plos One|August 3, 2017
Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasiaJoel Fedida, Veronique Fressart, Philippe Charron, et al.
European Heart Journal|June 16, 2009
Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathyLaëtitia Duboscq-Bidot, Philippe Charron, Volker Ruppert, et al.
Neuromuscular Disorders : NMD|December 14, 2011
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal studyKarim Wahbi, Anthony Béhin, Philippe Charron, et al.
JACC. Clinical Electrophysiology|March 15, 2025
Pulsed-Field vs Thermal Catheter Ablation of Atrial Fibrillation in Patients With Hypertrophic CardiomyopathySamy Gribissa, Thomas Kueffer, Sven Knecht, et al.
Stem Cell Research|February 20, 2021
Generation of iPSC line from MYH7 R403L mutation carrier with severe hypertrophic cardiomyopathy and isogenic CRISPR/Cas9 corrected controlVincent Fontaine, Laetitia Duboscq-Bidot, Charlène Jouve, et al.
Frontiers in Physiology|January 8, 2013
Brugada ECG pattern: a physiopathological prospective study based on clinical, electrophysiological, angiographic, and genetic findingsGuillaume Duthoit, Véronique Fressart, Françoise Hidden-Lucet, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|February 28, 2025
Imaging features of desmoplakin arrhythmogenic cardiomyopathy: A comparative cardiovascular magnetic resonance studyMikael Laredo, Etienne Charpentier, Shannon Soulez, et al.
Clinical Genetics|October 31, 2023
DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosisClaire Perret, Carole Proust, Ulrike Esslinger, et al.
Pageof 21

Showing results (71-80 of 203) with videos related to

Sort By:
Pageof 21
Microbiology Spectrum|March 26, 2026
Two novel real-time PCR assays for <i>Brucella</i> detection: a species-specific multiplex and a genus-level singleplex developed via large-scale whole genome sequencing data analysisEmily Hoover, John Chmara, Marc-Olivier Duceppe, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|May 27, 2021
Hypertrophic cardiomyopathies requiring more monitoring for less atrial fibrillation-related complications: a clustering analysis based on the French registry on hypertrophic cardiomyopathy (REMY)Marion Hourqueig, Guillaume Bouzille, Mariana Mirabel, et al.
Plos One|August 3, 2017
Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasiaJoel Fedida, Veronique Fressart, Philippe Charron, et al.
European Heart Journal|June 16, 2009
Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathyLaëtitia Duboscq-Bidot, Philippe Charron, Volker Ruppert, et al.
Neuromuscular Disorders : NMD|December 14, 2011
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal studyKarim Wahbi, Anthony Béhin, Philippe Charron, et al.
JACC. Clinical Electrophysiology|March 15, 2025
Pulsed-Field vs Thermal Catheter Ablation of Atrial Fibrillation in Patients With Hypertrophic CardiomyopathySamy Gribissa, Thomas Kueffer, Sven Knecht, et al.
Stem Cell Research|February 20, 2021
Generation of iPSC line from MYH7 R403L mutation carrier with severe hypertrophic cardiomyopathy and isogenic CRISPR/Cas9 corrected controlVincent Fontaine, Laetitia Duboscq-Bidot, Charlène Jouve, et al.
Frontiers in Physiology|January 8, 2013
Brugada ECG pattern: a physiopathological prospective study based on clinical, electrophysiological, angiographic, and genetic findingsGuillaume Duthoit, Véronique Fressart, Françoise Hidden-Lucet, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|February 28, 2025
Imaging features of desmoplakin arrhythmogenic cardiomyopathy: A comparative cardiovascular magnetic resonance studyMikael Laredo, Etienne Charpentier, Shannon Soulez, et al.
Clinical Genetics|October 31, 2023
DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosisClaire Perret, Carole Proust, Ulrike Esslinger, et al.
Pageof 21