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J Peter van Tintelen

Showing results (61-70 of 232) with videos related to

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Open Heart|October 22, 2014
Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathyMarijke Wasielewski, Karin Y van Spaendonck-Zwarts, Nico-Derk L Westerink, et al.
Journal of the American College of Cardiology|November 21, 2009
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysisArgelia Medeiros-Domingo, Zahurul A Bhuiyan, David J Tester, et al.
Journal of the American College of Cardiology|July 19, 2005
Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhoodGertie C M Beaufort-Krol, Maarten P van den Berg, Arthur A M Wilde, et al.
Heart Rhythm|February 7, 2018
Predicting arrhythmic risk in arrhythmogenic right ventricular cardiomyopathy: A systematic review and meta-analysisLaurens P Bosman, Arjan Sammani, Cynthia A James, et al.
American Journal of Medical Genetics. Part A|March 31, 2012
Diagnostic yield in adults screened at the Marfan outpatient clinic using the 1996 and 2010 Ghent nosologiesJan J J Aalberts, Chris H L Thio, Agnes G Schuurman, et al.
European Journal of Medical Genetics|August 28, 2007
Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin geneJorieke E H Bergman, Hermine E Veenstra-Knol, Anthonie J van Essen, et al.
Heart Rhythm|June 10, 2022
Value of genetic testing in the diagnosis and risk stratification of arrhythmogenic right ventricular cardiomyopathyRemco de Brouwer, Laurens P Bosman, Sophia Gripenstedt, et al.
Circulation|May 12, 2010
Peripartum cardiomyopathy as a part of familial dilated cardiomyopathyKarin Y van Spaendonck-Zwarts, J Peter van Tintelen, Dirk J van Veldhuisen, et al.
JACC. Clinical Electrophysiology|September 25, 2020
Prevalence and Prognostic Impact of Pathogenic Variants in Patients With Dilated Cardiomyopathy Referred for Ventricular Tachycardia AblationMicaela Ebert, Adrianus P Wijnmaalen, Marta de Riva, et al.
Human Mutation|July 2, 2009
A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathyPaul A van der Zwaag, Jan D H Jongbloed, Maarten P van den Berg, et al.
Pageof 24

Showing results (61-70 of 232) with videos related to

Sort By:
Pageof 24
Open Heart|October 22, 2014
Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathyMarijke Wasielewski, Karin Y van Spaendonck-Zwarts, Nico-Derk L Westerink, et al.
Journal of the American College of Cardiology|November 21, 2009
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysisArgelia Medeiros-Domingo, Zahurul A Bhuiyan, David J Tester, et al.
Journal of the American College of Cardiology|July 19, 2005
Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhoodGertie C M Beaufort-Krol, Maarten P van den Berg, Arthur A M Wilde, et al.
Heart Rhythm|February 7, 2018
Predicting arrhythmic risk in arrhythmogenic right ventricular cardiomyopathy: A systematic review and meta-analysisLaurens P Bosman, Arjan Sammani, Cynthia A James, et al.
American Journal of Medical Genetics. Part A|March 31, 2012
Diagnostic yield in adults screened at the Marfan outpatient clinic using the 1996 and 2010 Ghent nosologiesJan J J Aalberts, Chris H L Thio, Agnes G Schuurman, et al.
European Journal of Medical Genetics|August 28, 2007
Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin geneJorieke E H Bergman, Hermine E Veenstra-Knol, Anthonie J van Essen, et al.
Heart Rhythm|June 10, 2022
Value of genetic testing in the diagnosis and risk stratification of arrhythmogenic right ventricular cardiomyopathyRemco de Brouwer, Laurens P Bosman, Sophia Gripenstedt, et al.
Circulation|May 12, 2010
Peripartum cardiomyopathy as a part of familial dilated cardiomyopathyKarin Y van Spaendonck-Zwarts, J Peter van Tintelen, Dirk J van Veldhuisen, et al.
JACC. Clinical Electrophysiology|September 25, 2020
Prevalence and Prognostic Impact of Pathogenic Variants in Patients With Dilated Cardiomyopathy Referred for Ventricular Tachycardia AblationMicaela Ebert, Adrianus P Wijnmaalen, Marta de Riva, et al.
Human Mutation|July 2, 2009
A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathyPaul A van der Zwaag, Jan D H Jongbloed, Maarten P van den Berg, et al.
Pageof 24