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JAMA Cardiology|July 2, 2025
Location of LMNA Variants and Clinical Outcomes in CardiomyopathyAshwin Bhaskaran, Rabah Ben Yaou, Adam S Helms, et al.
European Journal of Preventive Cardiology|October 31, 2021
External validation of the HCM Risk-Kids model for predicting sudden cardiac death in childhood hypertrophic cardiomyopathyGabrielle Norrish, Chen Qu, Ella Field, et al.
Journal of the American College of Cardiology|March 19, 2013
Prevention of sudden cardiac death with implantable cardioverter-defibrillators in children and adolescents with hypertrophic cardiomyopathyBarry J Maron, Paolo Spirito, Michael J Ackerman, et al.
Circulation. Heart Failure|August 1, 2024
Quality of Life and Exercise Capacity in Early Stage and Subclinical Hypertrophic Cardiomyopathy: A Secondary Analysis of the VANISH TrialCatherine G Ireland, Danielle S Burstein, Sharlene M Day, et al.
JACC. Heart Failure|November 9, 2024
The Clinical Trajectory of NYHA Functional Class I Patients With Obstructive Hypertrophic CardiomyopathyMonica Ahluwalia, Jiankang Liu, Iacopo Olivotto, et al.
Circulation. Heart Failure|May 9, 2025
Proteomic Analysis of Valsartan for Attenuating Disease Evolution in Early Sarcomeric Hypertrophic Cardiomyopathy (VANISH) Clinical TrialConstantin-Cristian Topriceanu, Christoffer Rasmus Vissing, Anna Axelsson Raja, et al.
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