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JACC. Heart Failure|June 20, 2025
Aficamten Treatment for Symptomatic Obstructive Hypertrophic Cardiomyopathy: 48-Week Results From FOREST-HCMSara Saberi, Theodore P Abraham, Lubna Choudhury, et al.
Circulation. Genomic and Precision Medicine|February 10, 2021
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical FeaturesAlice Ghidoni, Perry M Elliott, Petros Syrris, et al.
JACC. Clinical Electrophysiology|May 10, 2024
Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic CardiomyopathyFrancisco J Bermudez-Jimenez, Alexandros Protonotarios, Soledad García-Hernández, et al.
Plos One|August 31, 2018
No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathyEdgar T Hoorntje, Anna Posafalvi, Petros Syrris, et al.
European Journal of Heart Failure|August 3, 2026
Long-Term Impact of Aficamten on Patient-Reported Outcome Measures in Obstructive Hypertrophic Cardiomyopathy: Results From FOREST-HCMShepard D Weiner, Lusha W Liang, Ahmad Masri, et al.
JACC. Advances|January 29, 2025
Naxos Disease and Related Cardio-Cutaneous SyndromesAlexandros Protonotarios, Angeliki Asimaki, Cristina Basso, et al.
Hepatology (Baltimore, Md.)|September 2, 2022
Characterization of Morreton virus as an oncolytic virotherapy platform for liver cancersBolni Marius Nagalo, Yumei Zhou, Emilien J Loeuillard, et al.
Human Mutation|May 4, 2021
New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency DisorderJustin O Szot, Anne Slavotinek, Karen Chong, et al.
Pain Research & Management|July 23, 2016
Research Priorities in the Field of Posttraumatic Pain and Disability: Results of a Transdisciplinary Consensus-Generating WorkshopDavid M Walton, James M Elliott, Joshua Lee, et al.
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