Background: Left ventricular noncompaction cardiomyopathy (LVNC CMP) is a genetic cardiomyopathy. Genotype-phenotype correlation and clinical outcome of genetic variants in pediatric and adult LVNC ...

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

The term dilated cardiomyopathy (DCM) refers to a spectrum of heterogeneous myocardial disorders that are characterized by ventricular dilation and depressed myocardial performance in the absence of ...

such as hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), arrhythmogenic right ventricular cardiomyopathy (ARVC), and left ventricular non-compaction (LVNC), and are defined by ...

Please View Select Publications from our faculty, graduate students, and research staff. Current research emphases in the pharmacology area include cardiovascular and renal pharmacology; cardiac ...

2 St George's University Hospital Foundation NHS Trust, London, UK Correspondence to Professor Sanjay Sharma, Department of Cardiovascular and Cell Sciences, St George's University of London, Cranmer ...

However, there are also documents emphasising that OAC could be considered in patients with specific NICM, such as those with Takotsubo syndrome, LV myocardial densification insufficiency, ...

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 ...

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 ...

Heart failure is a condition that occurs when the heart can’t pump as well as it should. This may happen when the heart muscle becomes weak or stiff. As a result, it doesn’t deliver enough blood to ...