Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Sven Dittmann

Showing results (31-40 of 39) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 39 results.
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.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 20, 2011
In vitro modeling of ryanodine receptor 2 dysfunction using human induced pluripotent stem cellsAzra Fatima, Guoxing Xu, Kaifeng Shao, 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.
European Heart Journal|July 2, 2025
Long QT syndrome in children and adolescents: risk factors and outcomes in a large German cohortLea Lippert, Tobias Burkard, Franziska Markel, 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.
Circulation|January 17, 2020
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic ConditionJason D Roberts, S Yukiko Asaki, Andrea Mazzanti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controlsRoddy Walsh, Najim Lahrouchi, Rafik Tadros, 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.
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.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
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.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 20, 2011
In vitro modeling of ryanodine receptor 2 dysfunction using human induced pluripotent stem cellsAzra Fatima, Guoxing Xu, Kaifeng Shao, 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.
European Heart Journal|July 2, 2025
Long QT syndrome in children and adolescents: risk factors and outcomes in a large German cohortLea Lippert, Tobias Burkard, Franziska Markel, 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.
Circulation|January 17, 2020
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic ConditionJason D Roberts, S Yukiko Asaki, Andrea Mazzanti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controlsRoddy Walsh, Najim Lahrouchi, Rafik Tadros, 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.
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.
Pageof 4