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Jeffrey Towbin

Showing results (11-20 of 20) with videos related to

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Circulation|March 1, 2006
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathyKalliopi Pilichou, Andrea Nava, Cristina Basso, et al.
Journal of Cardiovascular Electrophysiology|June 25, 2009
Genetic modulation of brugada syndrome by a common polymorphismEric Lizotte, M Juhani Junttila, Marie Pierre Dube, et al.
Pediatric Cardiology|May 7, 2024
Genetic Testing Resources and Practice Patterns Among Pediatric Cardiomyopathy ProgramsJustin Godown, Emily H Kim, Melanie D Everitt, et al.
European Journal of Medical Genetics|November 28, 2009
Paucity of skeletal manifestations in Hispanic families with FBN1 mutationsCarlos Villamizar, Ellen S Regalado, Van Tran Fadulu, et al.
Radiology|December 19, 2018
Left Ventricular Strain Is Abnormal in Preclinical and Overt Hypertrophic Cardiomyopathy: Cardiac MR Feature TrackingDavis M Vigneault, Eunice Yang, Patrick J Jensen, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|December 30, 2017
Left Atrial structure and function in hypertrophic cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophyHoshang Farhad, Sara B Seidelmann, Davis Vigneault, et al.
American Journal of Human Genetics|December 27, 2016
Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline MyopathySatoko Miyatake, Satomi Mitsuhashi, Yukiko K Hayashi, et al.
Journal of the American College of Cardiology|February 19, 2011
Risk factors for recurrent syncope and subsequent fatal or near-fatal events in children and adolescents with long QT syndromeJudy F Liu, Christian Jons, Arthur J Moss, et al.
International Journal of Cardiology. Heart & Vasculature|June 14, 2021
Young athletes: Preventing sudden death by adopting a modern screening approach? A critical review and the opening of a debatePaolo Angelini, Raja Muthupillai, Alberto Lopez, et al.
European Journal of Human Genetics : EJHG|January 10, 2019
Genetic architecture of laterality defects revealed by whole exome sequencingAlexander H Li, Neil A Hanchard, Mahshid Azamian, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Circulation|March 1, 2006
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathyKalliopi Pilichou, Andrea Nava, Cristina Basso, et al.
Journal of Cardiovascular Electrophysiology|June 25, 2009
Genetic modulation of brugada syndrome by a common polymorphismEric Lizotte, M Juhani Junttila, Marie Pierre Dube, et al.
Pediatric Cardiology|May 7, 2024
Genetic Testing Resources and Practice Patterns Among Pediatric Cardiomyopathy ProgramsJustin Godown, Emily H Kim, Melanie D Everitt, et al.
European Journal of Medical Genetics|November 28, 2009
Paucity of skeletal manifestations in Hispanic families with FBN1 mutationsCarlos Villamizar, Ellen S Regalado, Van Tran Fadulu, et al.
Radiology|December 19, 2018
Left Ventricular Strain Is Abnormal in Preclinical and Overt Hypertrophic Cardiomyopathy: Cardiac MR Feature TrackingDavis M Vigneault, Eunice Yang, Patrick J Jensen, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|December 30, 2017
Left Atrial structure and function in hypertrophic cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophyHoshang Farhad, Sara B Seidelmann, Davis Vigneault, et al.
American Journal of Human Genetics|December 27, 2016
Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline MyopathySatoko Miyatake, Satomi Mitsuhashi, Yukiko K Hayashi, et al.
Journal of the American College of Cardiology|February 19, 2011
Risk factors for recurrent syncope and subsequent fatal or near-fatal events in children and adolescents with long QT syndromeJudy F Liu, Christian Jons, Arthur J Moss, et al.
International Journal of Cardiology. Heart & Vasculature|June 14, 2021
Young athletes: Preventing sudden death by adopting a modern screening approach? A critical review and the opening of a debatePaolo Angelini, Raja Muthupillai, Alberto Lopez, et al.
European Journal of Human Genetics : EJHG|January 10, 2019
Genetic architecture of laterality defects revealed by whole exome sequencingAlexander H Li, Neil A Hanchard, Mahshid Azamian, et al.
Pageof 2