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Sven Dittmann

Showing results (1-10 of 39) with videos related to

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Heart Rhythm|August 1, 2018
Nonsynonymous TNNI3K mutations and phenotypes: More than a "simple" cardiomyopathySven Dittmann, Eric Schulze-Bahr
Advances in Experimental Medicine and Biology|June 17, 2024
Human Genetics of Cardiac ArrhythmiasEric Schulze-Bahr, Sven Dittmann
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 9, 2025
Cardiac arrhythmias and genetics - current stageSchulze-Bahr, Sven Dittmann, Janis Kerkering
Cardiovascular Research|February 22, 2021
Long, longer, long QT syndrome: what makes the difference?Sven Dittmann, Anne Kayser, Eric Schulze-Bahr
Frontiers in Cardiovascular Medicine|November 29, 2023
Case Report: Hypertrophic cardiomyopathy with recurrent episodes of ventricular fibrillation and concurrent sinus arrestJassin Hamidi, Joachim Winter, Rene Weber, et al.
Journal of Thoracic Disease|July 11, 2022
Non-syndromal mitral valve prolapse (MVP): a common entity, but not commonly associated with <i>DCHS1</i> or <i>FLNA</i> mutationsKatharina Uphoff, Sven Dittmann, Patricia Ott, et al.
Journal of Cardiovascular Translational Research|October 1, 2025
A MATLAB Algorithm to Automatically Estimate the QT Interval and Other ECG Parameters and Validation Using a Machine Learning Approach in Congenital Long-QT SyndromeElinor Tzvi-Minker, Sven Dittmann, Corinna Rickert, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|April 17, 2023
Case report: cosegregation of a TPM1 in-frame deletion (p.Lys7del) with familial non-compaction cardiomyopathy (NCCM)Yvonne Hanel, Sven Dittmann, Klara Müller, et al.
Stem Cell Research|October 27, 2023
Patient-derived stem cell line UKMi005-A (hiPSC) harboring a non-synonymous heterozygous KCNJ5 gene variantAnne Kayser, Sven Dittmann, Andreas van Impel, et al.
BMC Cardiovascular Disorders|April 14, 2021
A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutationsBenno Hartung, Anne Tank, Sven Dittmann, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Heart Rhythm|August 1, 2018
Nonsynonymous TNNI3K mutations and phenotypes: More than a "simple" cardiomyopathySven Dittmann, Eric Schulze-Bahr
Advances in Experimental Medicine and Biology|June 17, 2024
Human Genetics of Cardiac ArrhythmiasEric Schulze-Bahr, Sven Dittmann
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 9, 2025
Cardiac arrhythmias and genetics - current stageSchulze-Bahr, Sven Dittmann, Janis Kerkering
Cardiovascular Research|February 22, 2021
Long, longer, long QT syndrome: what makes the difference?Sven Dittmann, Anne Kayser, Eric Schulze-Bahr
Frontiers in Cardiovascular Medicine|November 29, 2023
Case Report: Hypertrophic cardiomyopathy with recurrent episodes of ventricular fibrillation and concurrent sinus arrestJassin Hamidi, Joachim Winter, Rene Weber, et al.
Journal of Thoracic Disease|July 11, 2022
Non-syndromal mitral valve prolapse (MVP): a common entity, but not commonly associated with <i>DCHS1</i> or <i>FLNA</i> mutationsKatharina Uphoff, Sven Dittmann, Patricia Ott, et al.
Journal of Cardiovascular Translational Research|October 1, 2025
A MATLAB Algorithm to Automatically Estimate the QT Interval and Other ECG Parameters and Validation Using a Machine Learning Approach in Congenital Long-QT SyndromeElinor Tzvi-Minker, Sven Dittmann, Corinna Rickert, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|April 17, 2023
Case report: cosegregation of a TPM1 in-frame deletion (p.Lys7del) with familial non-compaction cardiomyopathy (NCCM)Yvonne Hanel, Sven Dittmann, Klara Müller, et al.
Stem Cell Research|October 27, 2023
Patient-derived stem cell line UKMi005-A (hiPSC) harboring a non-synonymous heterozygous KCNJ5 gene variantAnne Kayser, Sven Dittmann, Andreas van Impel, et al.
BMC Cardiovascular Disorders|April 14, 2021
A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutationsBenno Hartung, Anne Tank, Sven Dittmann, et al.
Pageof 4