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Journal of Neuromuscular Diseases|February 16, 2024
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient CardiomyopathyLuca Bello, Daniele Sabbatini, Aurora Fusto, et al.Annals of Internal Medicine|September 3, 2019
Cardiac and Neuromuscular Features of Patients With LMNA-Related CardiomyopathyGiovanni Peretto, Chiara Di Resta, Jacopo Perversi, et al.Journal of Cardiovascular Medicine (Hagerstown, Md.)|June 27, 2025
Myosin-ATPase inhibitor in real-world patients with obstructive HCM: a report by the Cardiomyopathies and Pericardial Diseases WG of the Italian Society of CardiologyCesare de Gregorio, Paolo Bellocchi, Anna Rosa Napoli, et al.European Journal of Heart Failure|December 22, 2023
Real-world candidacy to mavacamten in a contemporary hypertrophic obstructive cardiomyopathy populationEdoardo Bertero, Chiara Chiti, Maria Alessandra Schiavo, et al.Pageof 4