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Flavie Ader

Showing results (31-40 of 41) with videos related to

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Journal of Clinical Medicine|May 10, 2020
Psychosocial Impact of Predictive Genetic Testing in Hereditary Heart Diseases: The PREDICT StudyCéline Bordet, Sandrine Brice, Carole Maupain, et al.
Circulation. Genomic and Precision Medicine|December 7, 2023
NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and PrognosisAlexis Hermida, Flavie Ader, Gilles Millat, et al.
JACC. Advances|June 28, 2024
Long-Term Arrhythmic Follow-Up and Risk Stratification of Patients With Desmoplakin-Associated Arrhythmogenic Right Ventricular CardiomyopathyAlessio Gasperetti, Richard Carrick, Alexandros Protonotarios, et al.
Heart Rhythm|August 12, 2024
Systematic analysis of SCN5A variants associated with inherited cardiac diseasesAlexis Hermida, Guillaume Jedraszak, Flavie Ader, et al.
JAMA Cardiology|May 12, 2021
Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart FailureMohammed Majid Akhtar, Massimiliano Lorenzini, Menelaos Pavlou, et al.
European Heart Journal|September 17, 2024
Clinical features and outcomes in carriers of pathogenic desmoplakin variantsAlessio Gasperetti, Richard T Carrick, Alexandros Protonotarios, et al.
European Heart Journal|July 16, 2024
A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriersRichard T Carrick, Alessio Gasperetti, Alexandros Protonotarios, et al.
Circulation|August 20, 2025
Prognostic Role of Myocarditis-Like Episodes and Their Treatment in Patients With Pathogenic Desmoplakin VariantsAlessio Gasperetti, Steven A Muller, Giovanni Peretto, et al.
European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Nature Genetics|January 26, 2021
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effectRafik Tadros, Catherine Francis, Xiao Xu, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Journal of Clinical Medicine|May 10, 2020
Psychosocial Impact of Predictive Genetic Testing in Hereditary Heart Diseases: The PREDICT StudyCéline Bordet, Sandrine Brice, Carole Maupain, et al.
Circulation. Genomic and Precision Medicine|December 7, 2023
NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and PrognosisAlexis Hermida, Flavie Ader, Gilles Millat, et al.
JACC. Advances|June 28, 2024
Long-Term Arrhythmic Follow-Up and Risk Stratification of Patients With Desmoplakin-Associated Arrhythmogenic Right Ventricular CardiomyopathyAlessio Gasperetti, Richard Carrick, Alexandros Protonotarios, et al.
Heart Rhythm|August 12, 2024
Systematic analysis of SCN5A variants associated with inherited cardiac diseasesAlexis Hermida, Guillaume Jedraszak, Flavie Ader, et al.
JAMA Cardiology|May 12, 2021
Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart FailureMohammed Majid Akhtar, Massimiliano Lorenzini, Menelaos Pavlou, et al.
European Heart Journal|September 17, 2024
Clinical features and outcomes in carriers of pathogenic desmoplakin variantsAlessio Gasperetti, Richard T Carrick, Alexandros Protonotarios, et al.
European Heart Journal|July 16, 2024
A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriersRichard T Carrick, Alessio Gasperetti, Alexandros Protonotarios, et al.
Circulation|August 20, 2025
Prognostic Role of Myocarditis-Like Episodes and Their Treatment in Patients With Pathogenic Desmoplakin VariantsAlessio Gasperetti, Steven A Muller, Giovanni Peretto, et al.
European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Nature Genetics|January 26, 2021
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effectRafik Tadros, Catherine Francis, Xiao Xu, et al.
Pageof 5