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Eric Schulze

Showing results (131-140 of 155) with videos related to

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Circulation. Genomic and Precision Medicine|August 21, 2019
Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated CardiomyopathyDerk Frank, Ashraf Yusuf Rangrez, Corinna Friedrich, et al.
Journal of Molecular and Cellular Cardiology|June 15, 2020
POPDC2 a novel susceptibility gene for conduction disordersSusanne Rinné, Beatriz Ortiz-Bonnin, Birgit Stallmeyer, et al.
Nature Genetics|October 19, 2004
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathyBrenda Gerull, Arnd Heuser, Thomas Wichter, et al.
Heart Rhythm|February 22, 2023
Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndromeMorten Krogh Christiansen, Kasper Kjær-Sørensen, Natacha C Clavsen, et al.
Circulation. Genomic and Precision Medicine|August 7, 2019
Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De NovoFreyja H M van Lint, Brittney Murray, Crystal Tichnell, et al.
Circulation. Cardiovascular Genetics|March 5, 2015
Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2Iris C R M Kolder, Michael W T Tanck, Pieter G Postema, et al.
Heart Rhythm|December 15, 2024
Novel risk predictor of arrhythmias for patients with potassium channel-related congenital long QT syndromeChristian Krijger Juárez, Virginnio M Proost, Michael W Tanck, et al.
Heart Rhythm|February 5, 2010
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testingJamie D Kapplinger, David J Tester, Marielle Alders, et al.
Circulation. Genomic and Precision Medicine|February 10, 2021
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical FeaturesAlice Ghidoni, Perry M Elliott, Petros Syrris, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|July 11, 2025
Current Management of Transition and Multidisciplinary Care of Patients with Inherited and Rare Cardiomyopathies in Europe: Results of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN GUARD-HEART)Emanuele Monda, Elena Biagini, Nico Blom, et al.
Pageof 16

Showing results (131-140 of 155) with videos related to

Sort By:
Pageof 16
Circulation. Genomic and Precision Medicine|August 21, 2019
Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated CardiomyopathyDerk Frank, Ashraf Yusuf Rangrez, Corinna Friedrich, et al.
Journal of Molecular and Cellular Cardiology|June 15, 2020
POPDC2 a novel susceptibility gene for conduction disordersSusanne Rinné, Beatriz Ortiz-Bonnin, Birgit Stallmeyer, et al.
Nature Genetics|October 19, 2004
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathyBrenda Gerull, Arnd Heuser, Thomas Wichter, et al.
Heart Rhythm|February 22, 2023
Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndromeMorten Krogh Christiansen, Kasper Kjær-Sørensen, Natacha C Clavsen, et al.
Circulation. Genomic and Precision Medicine|August 7, 2019
Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De NovoFreyja H M van Lint, Brittney Murray, Crystal Tichnell, et al.
Circulation. Cardiovascular Genetics|March 5, 2015
Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2Iris C R M Kolder, Michael W T Tanck, Pieter G Postema, et al.
Heart Rhythm|December 15, 2024
Novel risk predictor of arrhythmias for patients with potassium channel-related congenital long QT syndromeChristian Krijger Juárez, Virginnio M Proost, Michael W Tanck, et al.
Heart Rhythm|February 5, 2010
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testingJamie D Kapplinger, David J Tester, Marielle Alders, et al.
Circulation. Genomic and Precision Medicine|February 10, 2021
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical FeaturesAlice Ghidoni, Perry M Elliott, Petros Syrris, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|July 11, 2025
Current Management of Transition and Multidisciplinary Care of Patients with Inherited and Rare Cardiomyopathies in Europe: Results of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN GUARD-HEART)Emanuele Monda, Elena Biagini, Nico Blom, et al.
Pageof 16