arrhythmogenic right ventricular cardiomyopathy, and left ventricular noncompaction cardiomyopathy. They can be hereditary or acquired conditions. Genome-wide and multitrait analyses identify ...

Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD. (B.A., B.M., S.A.M., C.T., A.G., R.T.C., H.C., C.A.J., A.S ...

Department of Cell Biology, Duke University School of Medicine, Durham, NC. (R.M.P., A.P.L.) Division of Pediatric Cardiology, Department of Pediatrics, Duke ...

Barth syndrome (BTHS) is a rare genetic disease caused by mutations in the TAFAZZIN gene. It is characterized by neutropenia, cardiomyopathy and skeletal myopathy. Neutropenia in BTHS is associated ...

Chair and Professor of Medicinal Chemistry, Joseph P. & Shirley Shipman Buckley Endowed Professor of Drug Discovery Synthetic medicinal chemistry, structure-based design, natural product chemistry ...

Non-ischemic dilated cardiomyopathy (NIDCM) is the most common type of heart muscle disease in the world. However, most of what we know about it comes from studies in Western countries. There isn’t ...