Dilated cardiomyopathy (DCM) is a heterogeneous disorder that is familial in approximately 30% of cases. Although several genes have been identified that can cause familial DCM, molecular analyses ...

1 Department of Cardiology, The First Hospital of Jilin University, Changchun, China 2 Undergraduate School, Shanghai Jiao Tong University School of Medicine, Shanghai, China Dilated cardiomyopathy ...

yahoo.es To understand the key role of echocardiography in the diagnosis and management of hypertrophic cardiomyopathy (HCM). To learn the fundamental features that an echocardiographic report of a ...

The online databases Embase/Medline, PubMed/Medline were searched using the Medical Subject Headings (MeSH) terms “[(dilated cardiomyopathy OR DCM ... This systematic review has identified 4 ...

[27] All patients were classified into familial or nonfamilial DCM by echocardiography of the first-degree relatives. The mean age at study entry of the familial DCM group was not significantly ...

Limited data exist on cardiac adiposity in subjects with dilated cardiomyopathy (DCM). The aim of the study was to examine the components of cardiac steatosis and their relationship to LV structure ...

Hypertrophic cardiomyopathy treatment: What to expect, types of medications, surgeries and procedures, lifestyle changes, and more.

While clinicians draw from logical reasoning and experiential knowledge, AI models excel in processing vast, complex data streams across modalities like ECG, echocardiography ... and even ...

Division of Human Genetics, Department of Internal Medicine (H.N., J. Cao, D.D.K., E.J., J.M., J. Cowan, P.P., R.E.H.) The Davis Heart and Lung Research Institute (H ...

echocardiography, and cardiovascular MRI) with her first-degree relatives. Repeat cardiovascular MRI 12 months after the acute index presentation showed a mildly dilated left ventricle (end ...