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Alessandra Rampazzo

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Journal of the American College of Cardiology|July 11, 2002
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriersBarbara Bauce, Alessandra Rampazzo, Cristina Basso, et al.
European Heart Journal|June 9, 2005
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutationsBarbara Bauce, Cristina Basso, Alessandra Rampazzo, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genesAlessandra Rampazzo, Giorgia Beffagna, Andrea Nava, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|September 12, 2012
R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart diseaseGiorgia Beffagna, Antonella Cecchetto, Lucia Dal Bianco, et al.
Stem Cell Research|March 19, 2025
Generation of the human iPSC line UNIPDi006-A from a patient with arrhythmogenic cardiomyopathy carrying the DSG2 c.1672C > T pathogenic variantClaudia Sacchetto, Martina Rabino, Marianna Paulis, et al.
American Journal of Human Genetics|October 10, 2002
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathyAlessandra Rampazzo, Andrea Nava, Sandro Malacrida, et al.
Cardiovascular Research|January 11, 2005
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1Giorgia Beffagna, Gianluca Occhi, Andrea Nava, et al.
The American Journal of Cardiology|November 22, 2012
Desmin mutations and arrhythmogenic right ventricular cardiomyopathyAlessandra Lorenzon, Giorgia Beffagna, Barbara Bauce, et al.
Human Pathology|August 9, 2005
Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substratesGiulia d'Amati, Alessia Bagattin, Barbara Bauce, et al.
Circulation|March 1, 2006
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathyKalliopi Pilichou, Andrea Nava, Cristina Basso, et al.
Pageof 6

Showing results (21-30 of 60) with videos related to

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Pageof 6
Journal of the American College of Cardiology|July 11, 2002
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriersBarbara Bauce, Alessandra Rampazzo, Cristina Basso, et al.
European Heart Journal|June 9, 2005
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutationsBarbara Bauce, Cristina Basso, Alessandra Rampazzo, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genesAlessandra Rampazzo, Giorgia Beffagna, Andrea Nava, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|September 12, 2012
R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart diseaseGiorgia Beffagna, Antonella Cecchetto, Lucia Dal Bianco, et al.
Stem Cell Research|March 19, 2025
Generation of the human iPSC line UNIPDi006-A from a patient with arrhythmogenic cardiomyopathy carrying the DSG2 c.1672C > T pathogenic variantClaudia Sacchetto, Martina Rabino, Marianna Paulis, et al.
American Journal of Human Genetics|October 10, 2002
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathyAlessandra Rampazzo, Andrea Nava, Sandro Malacrida, et al.
Cardiovascular Research|January 11, 2005
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1Giorgia Beffagna, Gianluca Occhi, Andrea Nava, et al.
The American Journal of Cardiology|November 22, 2012
Desmin mutations and arrhythmogenic right ventricular cardiomyopathyAlessandra Lorenzon, Giorgia Beffagna, Barbara Bauce, et al.
Human Pathology|August 9, 2005
Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substratesGiulia d'Amati, Alessia Bagattin, Barbara Bauce, et al.
Circulation|March 1, 2006
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathyKalliopi Pilichou, Andrea Nava, Cristina Basso, et al.
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