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Marina Cerrone

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

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JACC. Clinical Electrophysiology|April 17, 2025
Long-Term Follow-Up Data on Flecainide Use as an Antiarrhythmic in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multicenter StudySean Gaine, Thomas Rolland, Babken Asatryan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 19, 2021
Correction to: The genetic architecture of Plakophilin 2 cardiomyopathyAnnika M Dries, Anna Kirillova, Chloe M Reuter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2021
The genetic architecture of Plakophilin 2 cardiomyopathyAnnika M Dries, Anna Kirillova, Chloe M Reuter, et al.
Cardiovascular Research|January 11, 2017
Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesisAnneline S J M Te Riele, Esperanza Agullo-Pascual, Cynthia A James, et al.
European Heart Journal|June 7, 2019
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, David J Tester, et al.
Circulation|July 25, 2024
Vigorous Exercise in Patients With Congenital Long QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS StudyRachel Lampert, Sharlene Day, Barbara Ainsworth, et al.
European Heart Journal|August 2, 2023
Clinical presentation of calmodulin mutations: the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, Mette Nyegaard, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Diagnostic Criteria and Disease Staging for Desmoplakin CardiomyopathyEric Smith, Alessio Gasperetti, Richard T Carrick, et al.
Nature Genetics|April 27, 2022
Author Correction: 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.
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 8

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

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Pageof 8
You have reached the last page of results.This site can display upto 80 results.
JACC. Clinical Electrophysiology|April 17, 2025
Long-Term Follow-Up Data on Flecainide Use as an Antiarrhythmic in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multicenter StudySean Gaine, Thomas Rolland, Babken Asatryan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 19, 2021
Correction to: The genetic architecture of Plakophilin 2 cardiomyopathyAnnika M Dries, Anna Kirillova, Chloe M Reuter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2021
The genetic architecture of Plakophilin 2 cardiomyopathyAnnika M Dries, Anna Kirillova, Chloe M Reuter, et al.
Cardiovascular Research|January 11, 2017
Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesisAnneline S J M Te Riele, Esperanza Agullo-Pascual, Cynthia A James, et al.
European Heart Journal|June 7, 2019
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, David J Tester, et al.
Circulation|July 25, 2024
Vigorous Exercise in Patients With Congenital Long QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS StudyRachel Lampert, Sharlene Day, Barbara Ainsworth, et al.
European Heart Journal|August 2, 2023
Clinical presentation of calmodulin mutations: the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, Mette Nyegaard, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Diagnostic Criteria and Disease Staging for Desmoplakin CardiomyopathyEric Smith, Alessio Gasperetti, Richard T Carrick, et al.
Nature Genetics|April 27, 2022
Author Correction: 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.
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.
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