Background: Apical hypertrophic cardiomyopathy (HCM) exhibits substantial heterogeneity in morphology and function. Purpose: To identify clinically meaningful phenotypic clusters using imaging ...
Dilated cardiomyopathy (DCM) is more prevalent among individuals of African descent, but a genetic basis for this increased risk has remained unclear. By integrating genomic and phenotypic data from ...
The following slide deck was published by HUTCHMED (China) Limited in conjunction with this event.
Mavacamten did not significantly improve exercise capacity as assessed by peak oxygen uptake or improve patient-reported health status compared with placebo in patients with symptomatic nonobstructive ...
Background Patients with hypertrophic cardiomyopathy (HCM) often reduce their physical activity due to concerns about sudden cardiac death. However, objective data on activity patterns in HCM, ...
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