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Wouter P Te Rijdt

Showing results (1-10 of 25) with videos related to

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European Journal of Human Genetics : EJHG|June 6, 2013
Clinical utility gene card for: arrhythmogenic right ventricular cardiomyopathy (ARVC)Wouter P Te Rijdt, Jan Dh Jongbloed, Rudolf A de Boer, et al.
Cardiovascular Research|September 29, 2017
Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesisEdgar T Hoorntje, Wouter P Te Rijdt, Cynthia A James, et al.
Circulation. Genomic and Precision Medicine|February 1, 2020
Deciduous Teeth as an Alternative DNA Source for Postmortem Genetic TestingWouter P Te Rijdt, René H P Mieremet, Thirsa Kraaijenbrink, et al.
American Journal of Physiology. Heart and Circulatory Physiology|July 18, 2020
Desmin is essential for the structure and function of the sinoatrial node: implications for increased arrhythmogenesisManolis Mavroidis, Nikolaos C Athanasiadis, Pavlos Rigas, et al.
Histopathology|March 13, 2016
Phospholamban p.Arg14del cardiomyopathy is characterized by phospholamban aggregates, aggresomes, and autophagic degradationWouter P Te Rijdt, J Peter van Tintelen, Aryan Vink, et al.
Circulation. Genomic and Precision Medicine|May 22, 2019
Dyssynchronopathy Can be a Manifestation of Heritable CardiomyopathyWouter P Te Rijdt, Yvonne M Hoedemaekers, Jan D H Jongbloed, et al.
Journal of Cellular and Molecular Medicine|February 19, 2021
P62-positive aggregates are homogenously distributed in the myocardium and associated with the type of mutation in genetic cardiomyopathyZoë Joy van der Klooster, Shahrzad Sepehrkhouy, Dennis Dooijes, et al.
Plos One|April 16, 2014
High resolution systematic digital histological quantification of cardiac fibrosis and adipose tissue in phospholamban p.Arg14del mutation associated cardiomyopathyJohannes M I H Gho, René van Es, Nikolas Stathonikos, 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.
Open Heart|May 28, 2025
Assessing the psychometric properties of generic (EQ-5D-5L) and disease-specific (KCCQ) quality of life in patients with hypertrophic cardiomyopathy in the AFFECT-HCM studyIsabell Wiethoff, Stephan A C Schoonvelde, Rudolf A de Boer, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
European Journal of Human Genetics : EJHG|June 6, 2013
Clinical utility gene card for: arrhythmogenic right ventricular cardiomyopathy (ARVC)Wouter P Te Rijdt, Jan Dh Jongbloed, Rudolf A de Boer, et al.
Cardiovascular Research|September 29, 2017
Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesisEdgar T Hoorntje, Wouter P Te Rijdt, Cynthia A James, et al.
Circulation. Genomic and Precision Medicine|February 1, 2020
Deciduous Teeth as an Alternative DNA Source for Postmortem Genetic TestingWouter P Te Rijdt, René H P Mieremet, Thirsa Kraaijenbrink, et al.
American Journal of Physiology. Heart and Circulatory Physiology|July 18, 2020
Desmin is essential for the structure and function of the sinoatrial node: implications for increased arrhythmogenesisManolis Mavroidis, Nikolaos C Athanasiadis, Pavlos Rigas, et al.
Histopathology|March 13, 2016
Phospholamban p.Arg14del cardiomyopathy is characterized by phospholamban aggregates, aggresomes, and autophagic degradationWouter P Te Rijdt, J Peter van Tintelen, Aryan Vink, et al.
Circulation. Genomic and Precision Medicine|May 22, 2019
Dyssynchronopathy Can be a Manifestation of Heritable CardiomyopathyWouter P Te Rijdt, Yvonne M Hoedemaekers, Jan D H Jongbloed, et al.
Journal of Cellular and Molecular Medicine|February 19, 2021
P62-positive aggregates are homogenously distributed in the myocardium and associated with the type of mutation in genetic cardiomyopathyZoë Joy van der Klooster, Shahrzad Sepehrkhouy, Dennis Dooijes, et al.
Plos One|April 16, 2014
High resolution systematic digital histological quantification of cardiac fibrosis and adipose tissue in phospholamban p.Arg14del mutation associated cardiomyopathyJohannes M I H Gho, René van Es, Nikolas Stathonikos, 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.
Open Heart|May 28, 2025
Assessing the psychometric properties of generic (EQ-5D-5L) and disease-specific (KCCQ) quality of life in patients with hypertrophic cardiomyopathy in the AFFECT-HCM studyIsabell Wiethoff, Stephan A C Schoonvelde, Rudolf A de Boer, et al.
Pageof 3