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Pathogens (Basel, Switzerland)|May 28, 2022
Lyme Carditis: From Pathophysiology to Clinical ManagementCinzia Radesich, Eva Del Mestre, Kristen Medo, et al.ESC Heart Failure|August 24, 2022
Sex differences in natural history of cardiovascular magnetic resonance- and biopsy-proven lymphocytic myocarditisMatteo Castrichini, Aldostefano Porcari, Chiara Baggio, 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 the American College of Cardiology|November 17, 2022
Prognostic Prediction of Genotype vs Phenotype in Genetic CardiomyopathiesAlessia Paldino, Matteo Dal Ferro, Davide Stolfo, et al.Journal of the American College of Cardiology|May 8, 2024
Magnetic Resonance Imaging Characterization and Clinical Outcomes of Dilated and Arrhythmogenic Left Ventricular CardiomyopathiesMatteo Castrichini, Antonio De Luca, Giulia De Angelis, et al.European Journal of Heart Failure|September 12, 2025
Impact of genotype-phenotype associations on prognosis in dilated cardiomyopathySophie L V M Stroeks, Ping Wang, Marco Merlo, et al.European Heart Journal|August 28, 2023
Emery-Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failureDouglas E Cannie, Petros Syrris, Alexandros Protonotarios, et al.Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
The contribution of RBM20 truncating variants to human cardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.JACC. Advances|June 28, 2024
Long-Term Arrhythmic Follow-Up and Risk Stratification of Patients With Desmoplakin-Associated Arrhythmogenic Right Ventricular CardiomyopathyAlessio Gasperetti, Richard Carrick, Alexandros Protonotarios, et al.JAMA Cardiology|April 8, 2026
RBM20 Truncating Variants and Human CardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.Pageof 2