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J Peter van Tintelen

Showing results (91-100 of 232) with videos related to

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Patient Education and Counseling|March 20, 2025
DNA-poli: Design and development of a digital platform for family communication support and predictive genetic counseling on inherited diseasesTessa C Beinema, Marlies N van Lingen, Lieke M van den Heuvel, et al.
Circulation. Genomic and Precision Medicine|October 20, 2022
Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General PopulationMimount Bourfiss, Marion van Vugt, Abdulrahman I Alasiri, et al.
Heart Rhythm|December 25, 2015
QRS prolongation after premature stimulation is associated with polymorphic ventricular tachycardia in nonischemic cardiomyopathy: Results from the Leiden Nonischemic Cardiomyopathy StudySebastiaan R D Piers, Saïd F A Askar, Jeroen Venlet, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 20, 2024
Absence of an increased wall thickness does not rule out cardiac amyloidosisSteven A Muller, Anouk Achten, Manon G van der Meer, et al.
Journal of Cardiovascular Electrophysiology|April 1, 2008
Activation delay and VT parameters in arrhythmogenic right ventricular dysplasia/cardiomyopathy: toward improvement of diagnostic ECG criteriaMoniek G P J Cox, Marcel R Nelen, Arthur A M Wilde, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|February 15, 2019
Distinct molecular signature of phospholamban p.Arg14del arrhythmogenic cardiomyopathyWouter P Te Rijdt, Angeliki Asimaki, Jan D H Jongbloed, et al.
Heart Rhythm|May 3, 2008
Familial disease with a risk of sudden death: a longitudinal study of the psychological consequences of predictive testing for long QT syndromeKarin S W H Hendriks, Margriet M W B Hendriks, Erwin Birnie, et al.
European Heart Journal|August 29, 2015
Approach to family screening in arrhythmogenic right ventricular dysplasia/cardiomyopathyAnneline S J M te Riele, Cynthia A James, Judith A Groeneweg, et al.
Heart Rhythm|February 17, 2020
Clinical characteristics and determinants of the phenotype in TMEM43 arrhythmogenic right ventricular cardiomyopathy type 5Fernando Dominguez, Esther Zorio, Juan Jimenez-Jaimez, et al.
Genes|October 17, 2020
Genetic Evaluation in a Cohort of 126 Dutch Pulmonary Arterial Hypertension PatientsLieke M van den Heuvel, Samara M A Jansen, Suzanne I M Alsters, et al.
Pageof 24

Showing results (91-100 of 232) with videos related to

Sort By:
Pageof 24
Patient Education and Counseling|March 20, 2025
DNA-poli: Design and development of a digital platform for family communication support and predictive genetic counseling on inherited diseasesTessa C Beinema, Marlies N van Lingen, Lieke M van den Heuvel, et al.
Circulation. Genomic and Precision Medicine|October 20, 2022
Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General PopulationMimount Bourfiss, Marion van Vugt, Abdulrahman I Alasiri, et al.
Heart Rhythm|December 25, 2015
QRS prolongation after premature stimulation is associated with polymorphic ventricular tachycardia in nonischemic cardiomyopathy: Results from the Leiden Nonischemic Cardiomyopathy StudySebastiaan R D Piers, Saïd F A Askar, Jeroen Venlet, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 20, 2024
Absence of an increased wall thickness does not rule out cardiac amyloidosisSteven A Muller, Anouk Achten, Manon G van der Meer, et al.
Journal of Cardiovascular Electrophysiology|April 1, 2008
Activation delay and VT parameters in arrhythmogenic right ventricular dysplasia/cardiomyopathy: toward improvement of diagnostic ECG criteriaMoniek G P J Cox, Marcel R Nelen, Arthur A M Wilde, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|February 15, 2019
Distinct molecular signature of phospholamban p.Arg14del arrhythmogenic cardiomyopathyWouter P Te Rijdt, Angeliki Asimaki, Jan D H Jongbloed, et al.
Heart Rhythm|May 3, 2008
Familial disease with a risk of sudden death: a longitudinal study of the psychological consequences of predictive testing for long QT syndromeKarin S W H Hendriks, Margriet M W B Hendriks, Erwin Birnie, et al.
European Heart Journal|August 29, 2015
Approach to family screening in arrhythmogenic right ventricular dysplasia/cardiomyopathyAnneline S J M te Riele, Cynthia A James, Judith A Groeneweg, et al.
Heart Rhythm|February 17, 2020
Clinical characteristics and determinants of the phenotype in TMEM43 arrhythmogenic right ventricular cardiomyopathy type 5Fernando Dominguez, Esther Zorio, Juan Jimenez-Jaimez, et al.
Genes|October 17, 2020
Genetic Evaluation in a Cohort of 126 Dutch Pulmonary Arterial Hypertension PatientsLieke M van den Heuvel, Samara M A Jansen, Suzanne I M Alsters, et al.
Pageof 24