We investigated left ventricular (LV) remodeling, mechanics, systolic and diastolic function, combined with clinical characteristics and heart-failure treatment in association to death or heart-transplant (DoT) in pediatric idiopathic, genetic or familial dilated cardiomyopathy (DCM), using interpretable machine-learning.
Key Contact:
The Alliance is committed to fostering collaboration and knowledge-sharing across the donation and transplantation community. Research and materials shared on this page are contributed by individual authors and organizations. While we aim to provide a valuable forum for exchange, submissions are not formally reviewed or endorsed by The Alliance. The perspectives expressed belong solely to the authors, and users are encouraged to review content thoughtfully and in the context of their own professional judgment.
