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J Peter van Tintelen

Showing results (131-140 of 232) with videos related to

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Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|July 20, 2023
Exercise does not influence development of phenotype in PLN p.(Arg14del) cardiomyopathyFreyja H M van Lint, Fahima Hassanzada, Tom E Verstraelen, et al.
European Heart Journal|February 22, 2014
Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathyKarin Y van Spaendonck-Zwarts, Anna Posafalvi, Maarten P van den Berg, et al.
Heart (British Cardiac Society)|January 1, 2016
Pregnancy course and outcomes in women with arrhythmogenic right ventricular cardiomyopathyAnke R Hodes, Crystal Tichnell, Anneline S J M Te Riele, et al.
Circulation. Arrhythmia and Electrophysiology|March 11, 2010
Arrhythmogenic right ventricular dysplasia/cardiomyopathy diagnostic task force criteria: impact of new task force criteriaMoniek G P J Cox, Jasper J van der Smagt, Maartje Noorman, et al.
Journal of the American College of Cardiology|June 4, 2011
Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noiseJamie D Kapplinger, Andrew P Landstrom, Benjamin A Salisbury, et al.
American Heart Journal|November 24, 2007
High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinicsJ Peter van Tintelen, Robert M W Hofstra, Hilga Katerberg, et al.
Brain : a Journal of Neurology|February 1, 2013
Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathyMarian A J Weterman, Peter G Barth, Karin Y van Spaendonck-Zwarts, et al.
Science Translational Medicine|April 29, 2026
Dipeptidyl aminopeptidase-like protein 6 regulates the <i>I</i><sub>Na</sub>-<i>I</i><sub>to</sub> balance influencing cardiac electrophysiology and arrhythmogenesisAlberto Rossetti, Job Stoks, Roel L H M G Spätjens, et al.
Heart Rhythm|February 21, 2017
Cardiac phenotype and long-term prognosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia patients with late presentationAditya Bhonsale, Anneline S J M Te Riele, Abhishek C Sawant, et al.
European Journal of Heart Failure|January 26, 2013
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experienceKarin Y van Spaendonck-Zwarts, Ingrid A W van Rijsingen, Maarten P van den Berg, et al.
Pageof 24

Showing results (131-140 of 232) with videos related to

Sort By:
Pageof 24
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|July 20, 2023
Exercise does not influence development of phenotype in PLN p.(Arg14del) cardiomyopathyFreyja H M van Lint, Fahima Hassanzada, Tom E Verstraelen, et al.
European Heart Journal|February 22, 2014
Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathyKarin Y van Spaendonck-Zwarts, Anna Posafalvi, Maarten P van den Berg, et al.
Heart (British Cardiac Society)|January 1, 2016
Pregnancy course and outcomes in women with arrhythmogenic right ventricular cardiomyopathyAnke R Hodes, Crystal Tichnell, Anneline S J M Te Riele, et al.
Circulation. Arrhythmia and Electrophysiology|March 11, 2010
Arrhythmogenic right ventricular dysplasia/cardiomyopathy diagnostic task force criteria: impact of new task force criteriaMoniek G P J Cox, Jasper J van der Smagt, Maartje Noorman, et al.
Journal of the American College of Cardiology|June 4, 2011
Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noiseJamie D Kapplinger, Andrew P Landstrom, Benjamin A Salisbury, et al.
American Heart Journal|November 24, 2007
High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinicsJ Peter van Tintelen, Robert M W Hofstra, Hilga Katerberg, et al.
Brain : a Journal of Neurology|February 1, 2013
Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathyMarian A J Weterman, Peter G Barth, Karin Y van Spaendonck-Zwarts, et al.
Science Translational Medicine|April 29, 2026
Dipeptidyl aminopeptidase-like protein 6 regulates the <i>I</i><sub>Na</sub>-<i>I</i><sub>to</sub> balance influencing cardiac electrophysiology and arrhythmogenesisAlberto Rossetti, Job Stoks, Roel L H M G Spätjens, et al.
Heart Rhythm|February 21, 2017
Cardiac phenotype and long-term prognosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia patients with late presentationAditya Bhonsale, Anneline S J M Te Riele, Abhishek C Sawant, et al.
European Journal of Heart Failure|January 26, 2013
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experienceKarin Y van Spaendonck-Zwarts, Ingrid A W van Rijsingen, Maarten P van den Berg, et al.
Pageof 24