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Matteo Dal Ferro

Showing results (51-60 of 93) with videos related to

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European Heart Journal Supplements : Journal of the European Society of Cardiology|April 18, 2025
Fenotypic expressions and clinical manifestations of arrhythmogenic cardiomyopathyMartina Setti, Antonio De Luca, Alessia Paldino, et al.
Giornale Italiano Di Cardiologia (2006)|October 27, 2022
[The Regional Registry of Sudden Cardiac Death of Friuli Venezia Giulia. Protocols, best practices and results of a multidisciplinary project]Stefano D'Errico, Pier Riccardo Bergamini, Paolo Fattorini, et al.
Nature Communications|May 24, 2019
The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathyNicolò Salvarani, Silvia Crasto, Michele Miragoli, et al.
The Canadian Journal of Cardiology|July 17, 2021
Prevalence and Evolution of Right Ventricular Dysfunction Among Different Genetic Backgrounds in Dilated CardiomyopathyPaolo Manca, Antonio Cannatà, Vincenzo Nuzzi, et al.
Frontiers in Cardiovascular Medicine|November 24, 2022
Evolving trends in epidemiology and natural history of cardiac amyloidosis: 30-year experience from a tertiary referral center for cardiomyopathiesAldostefano Porcari, Valentina Allegro, Riccardo Saro, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|August 3, 2020
Management of nonischemic-dilated cardiomyopathies in clinical practice: a position paper of the working group on myocardial and pericardial diseases of Italian Society of CardiologyMarco Merlo, Marco Masè, Antonio Cannatà, et al.
JACC. Clinical Electrophysiology|May 25, 2024
Impact of DCM-Causing Genetic Background on Long-Term Response to Cardiac Resynchronization TherapyMatteo Dal Ferro, Alessia Paldino, Caterina Gregorio, et al.
Circulation. Cardiovascular Imaging|April 2, 2024
Cardiac Magnetic Resonance Feature-Tracking Identifies Preclinical Abnormalities in Hypertrophic Cardiomyopathy Sarcomere Gene Mutation CarriersFrancesco Negri, Giuseppe Damiano Sanna, Giulia Di Giovanna, et al.
European Journal of Heart Failure|February 26, 2024
Role of arrhythmic phenotype in prognostic stratification and management of dilated cardiomyopathyMartina Setti, Marco Merlo, Marta Gigli, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|May 29, 2009
Natural history of dilated cardiomyopathy: from asymptomatic left ventricular dysfunction to heart failure--a subgroup analysis from the Trieste Cardiomyopathy RegistryAneta Aleksova, Gastone Sabbadini, Marco Merlo, et al.
Pageof 10

Showing results (51-60 of 93) with videos related to

Sort By:
Pageof 10
European Heart Journal Supplements : Journal of the European Society of Cardiology|April 18, 2025
Fenotypic expressions and clinical manifestations of arrhythmogenic cardiomyopathyMartina Setti, Antonio De Luca, Alessia Paldino, et al.
Giornale Italiano Di Cardiologia (2006)|October 27, 2022
[The Regional Registry of Sudden Cardiac Death of Friuli Venezia Giulia. Protocols, best practices and results of a multidisciplinary project]Stefano D'Errico, Pier Riccardo Bergamini, Paolo Fattorini, et al.
Nature Communications|May 24, 2019
The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathyNicolò Salvarani, Silvia Crasto, Michele Miragoli, et al.
The Canadian Journal of Cardiology|July 17, 2021
Prevalence and Evolution of Right Ventricular Dysfunction Among Different Genetic Backgrounds in Dilated CardiomyopathyPaolo Manca, Antonio Cannatà, Vincenzo Nuzzi, et al.
Frontiers in Cardiovascular Medicine|November 24, 2022
Evolving trends in epidemiology and natural history of cardiac amyloidosis: 30-year experience from a tertiary referral center for cardiomyopathiesAldostefano Porcari, Valentina Allegro, Riccardo Saro, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|August 3, 2020
Management of nonischemic-dilated cardiomyopathies in clinical practice: a position paper of the working group on myocardial and pericardial diseases of Italian Society of CardiologyMarco Merlo, Marco Masè, Antonio Cannatà, et al.
JACC. Clinical Electrophysiology|May 25, 2024
Impact of DCM-Causing Genetic Background on Long-Term Response to Cardiac Resynchronization TherapyMatteo Dal Ferro, Alessia Paldino, Caterina Gregorio, et al.
Circulation. Cardiovascular Imaging|April 2, 2024
Cardiac Magnetic Resonance Feature-Tracking Identifies Preclinical Abnormalities in Hypertrophic Cardiomyopathy Sarcomere Gene Mutation CarriersFrancesco Negri, Giuseppe Damiano Sanna, Giulia Di Giovanna, et al.
European Journal of Heart Failure|February 26, 2024
Role of arrhythmic phenotype in prognostic stratification and management of dilated cardiomyopathyMartina Setti, Marco Merlo, Marta Gigli, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|May 29, 2009
Natural history of dilated cardiomyopathy: from asymptomatic left ventricular dysfunction to heart failure--a subgroup analysis from the Trieste Cardiomyopathy RegistryAneta Aleksova, Gastone Sabbadini, Marco Merlo, et al.
Pageof 10