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Matilde Karakachoff

Showing results (31-40 of 37) with videos related to

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European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.
European Heart Journal|October 12, 2017
New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome studyThierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, et al.
Medrxiv : the Preprint Server for Health Sciences|November 1, 2024
Isolated prolapse of the posterior mitral valve leaflet: phenotypic refinement, heritability and genetic etiologyAntoine Rimbert, Damien Duval, Daniel Trujillano, et al.
Nature Communications|August 7, 2024
Human genetic structure in Northwest France provides new insights into West European historical demographyIsabel Alves, Joanna Giemza, Michael G B Blum, et al.
Circulation. Genomic and Precision Medicine|May 13, 2022
Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International StudyMarine Tortigue, Lynne E Nield, Matilde Karakachoff, et al.
Journal of Personalized Medicine|September 23, 2022
Intracranial Aneurysm Classifier Using Phenotypic Factors: An International Pooled AnalysisSandrine Morel, Isabel C Hostettler, Georg R Spinner, et al.
Nature Genetics|February 25, 2022
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibilityJulien Barc, Rafik Tadros, Charlotte Glinge, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.
European Heart Journal|October 12, 2017
New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome studyThierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, et al.
Medrxiv : the Preprint Server for Health Sciences|November 1, 2024
Isolated prolapse of the posterior mitral valve leaflet: phenotypic refinement, heritability and genetic etiologyAntoine Rimbert, Damien Duval, Daniel Trujillano, et al.
Nature Communications|August 7, 2024
Human genetic structure in Northwest France provides new insights into West European historical demographyIsabel Alves, Joanna Giemza, Michael G B Blum, et al.
Circulation. Genomic and Precision Medicine|May 13, 2022
Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International StudyMarine Tortigue, Lynne E Nield, Matilde Karakachoff, et al.
Journal of Personalized Medicine|September 23, 2022
Intracranial Aneurysm Classifier Using Phenotypic Factors: An International Pooled AnalysisSandrine Morel, Isabel C Hostettler, Georg R Spinner, et al.
Nature Genetics|February 25, 2022
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibilityJulien Barc, Rafik Tadros, Charlotte Glinge, et al.
Pageof 4