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Journal of the American College of Cardiology|November 11, 2025
Danicamtiv, a Selective Agonist of Cardiac Myosin, for Dilated Cardiomyopathy: A Phase 2 Open-Label TrialNeal K Lakdawala, Ray E Hershberger, Pablo Garcia-Pavia, et al.European Heart Journal. Quality of Care & Clinical Outcomes|July 11, 2025
Current Management of Transition and Multidisciplinary Care of Patients with Inherited and Rare Cardiomyopathies in Europe: Results of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN GUARD-HEART)Emanuele Monda, Elena Biagini, Nico Blom, 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.European Journal of Human Genetics : EJHG|January 8, 2026
Domain-specific phenotypic profiles in RAF1-related Noonan syndromeAndrea Gazzin, Marta Calvo, Federico Rondot, et al.Circulation. Genomic and Precision Medicine|August 18, 2023
Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 VariantsDouglas E Cannie, Alexandros Protonotarios, Athanasios Bakalakos, et al.Plos One|September 29, 2025
Statin effect on arrhythmogenic cardiomyopathy disease progression (SEARCH): Randomized clinical study protocolElena Sommariva, Melania Lippi, Flavia Bruttini, et al.European Heart Journal|June 29, 2022
Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculatorAlexandros Protonotarios, Riccardo Bariani, Chiara Cappelletto, et al.Hellenic Journal of Cardiology : HJC = Hellenike Kardiologike Epitheorese|May 2, 2025
NAXCARE: a clinical outcome registry for Naxos disease and related cardiocutaneous syndromesAdalena Tsatsopoulou, Dominic Jr Abrams, Aris Anastasakis, et al.Circulation|January 5, 2026
Clinical Spectrum of Children With Parvovirus B19-Associated Acute MyocarditisEnrico Ammirati, Giacomo Veronese, Francesca Raimondi, et al.European Journal of Heart Failure|November 29, 2025
Clinical phenotype and prognosis of real-world patients with wild-type transthyretin amyloid cardiomyopathy treated with tafamidisAldostefano Porcari, Paolo Milani, Simone Longhi, et al.Pageof 15