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JACC. Heart Failure|August 23, 2025
Disease Penetrance in Genotype-Positive But Clinically Unaffected Relatives From Families With Dilated CardiomyopathyDouglas E Cannie, Athanasios Bakalakos, Petros Syrris, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|September 3, 2023
A cost-effectiveness analysis of hypertrophic cardiomyopathy sudden cardiac death risk algorithms for implantable cardioverter defibrillator decision-makingNathan Green, Yang Chen, Constantinos O'Mahony, et al.
JAMA Cardiology|August 28, 2024
Prevalence, Cardiac Phenotype, and Outcomes of Transthyretin Variants in the UK Biobank PopulationNay Aung, Hannah L Nicholls, C Anwar A Chahal, et al.
Circulation. Heart Failure|July 21, 2023
Targeted Therapies in Pediatric and Adult Patients With Hypertrophic Heart Disease: From Molecular Pathophysiology to Personalized MedicineEmanuele Monda, Athanasios Bakalakos, Marta Rubino, et al.
European Heart Journal|October 16, 2013
A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD)Constantinos O'Mahony, Fatima Jichi, Menelaos Pavlou, et al.
European Journal of Heart Failure|November 20, 2022
Effect of beta-blocker therapy on the response to mavacamten in patients with symptomatic obstructive hypertrophic cardiomyopathyMatthew T Wheeler, Daniel Jacoby, Perry M Elliott, et al.
Heart (British Cardiac Society)|October 30, 2014
Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathyLuis R Lopes, Petros Syrris, Oliver P Guttmann, et al.
Molecular Genetics and Metabolism|November 11, 2018
The effect of enzyme replacement therapy on clinical outcomes in female patients with Fabry disease - A systematic literature review by a European panel of expertsDominique P Germain, Michael Arad, Alessandro Burlina, et al.
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