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Alessandra Rampazzo

Showing results (31-40 of 60) with videos related to

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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|September 13, 2025
Givinostat inhibits in vitro differentiation of cardiac fibroadipogenic precursors from a mouse model of arrhythmogenic cardiomyopathySara Vencato, Chiara Romanato, Monica Forino, et al.
The American Journal of Cardiology|January 7, 2012
Follow-up with exercise test of effort-induced ventricular arrhythmias linked to ryanodine receptor type 2 gene mutationsAlexandros Klavdios Steriotis, Andrea Nava, Alessandra Rampazzo, et al.
Stem Cell Research|September 1, 2024
Generation of a human induced pluripotent stem cell line UGENTi002-A from an arrhythmogenic cardiomyopathy patient carrying the c.817C>T DSP heterozygous variant and isogenic control using CRISPR/Cas9 editingLaurens Léger, Jeffrey Aalders, Nina Heymans, et al.
The American Journal of Cardiology|October 23, 2008
Comparison of clinical features of arrhythmogenic right ventricular cardiomyopathy in men versus womenBarbara Bauce, Gianfranco Frigo, Frank I Marcus, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|July 4, 2015
Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathyAlessandro Zorzi, Ilaria Rigato, Kalliopi Pilichou, et al.
Journal of the American Heart Association|September 17, 2021
Evolving Diagnostic Criteria for Arrhythmogenic CardiomyopathyDomenico Corrado, Alessandro Zorzi, Alberto Cipriani, et al.
Plos One|April 4, 2015
Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathyCinzia Forleo, Monica Carmosino, Nicoletta Resta, et al.
European Journal of Human Genetics : EJHG|March 4, 2010
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathyMarzia De Bortoli, Giorgia Beffagna, Barbara Bauce, et al.
European Journal of Human Genetics : EJHG|July 13, 2017
Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathyMarzia De Bortoli, Chiara Calore, Alessandra Lorenzon, et al.
Heart Rhythm|February 5, 2010
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasiaBarbara Bauce, Andrea Nava, Giorgia Beffagna, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|September 13, 2025
Givinostat inhibits in vitro differentiation of cardiac fibroadipogenic precursors from a mouse model of arrhythmogenic cardiomyopathySara Vencato, Chiara Romanato, Monica Forino, et al.
The American Journal of Cardiology|January 7, 2012
Follow-up with exercise test of effort-induced ventricular arrhythmias linked to ryanodine receptor type 2 gene mutationsAlexandros Klavdios Steriotis, Andrea Nava, Alessandra Rampazzo, et al.
Stem Cell Research|September 1, 2024
Generation of a human induced pluripotent stem cell line UGENTi002-A from an arrhythmogenic cardiomyopathy patient carrying the c.817C>T DSP heterozygous variant and isogenic control using CRISPR/Cas9 editingLaurens Léger, Jeffrey Aalders, Nina Heymans, et al.
The American Journal of Cardiology|October 23, 2008
Comparison of clinical features of arrhythmogenic right ventricular cardiomyopathy in men versus womenBarbara Bauce, Gianfranco Frigo, Frank I Marcus, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|July 4, 2015
Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathyAlessandro Zorzi, Ilaria Rigato, Kalliopi Pilichou, et al.
Journal of the American Heart Association|September 17, 2021
Evolving Diagnostic Criteria for Arrhythmogenic CardiomyopathyDomenico Corrado, Alessandro Zorzi, Alberto Cipriani, et al.
Plos One|April 4, 2015
Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathyCinzia Forleo, Monica Carmosino, Nicoletta Resta, et al.
European Journal of Human Genetics : EJHG|March 4, 2010
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathyMarzia De Bortoli, Giorgia Beffagna, Barbara Bauce, et al.
European Journal of Human Genetics : EJHG|July 13, 2017
Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathyMarzia De Bortoli, Chiara Calore, Alessandra Lorenzon, et al.
Heart Rhythm|February 5, 2010
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasiaBarbara Bauce, Andrea Nava, Giorgia Beffagna, et al.
Pageof 6