Arrhythmogenic right ventricular cardiomyopathy

By Roopali Soni, Y. Oade. BMJ Case Reports, 2011

864 citations recorded by the source corpus.

Subfields: Cardiology and Cardiovascular Medicine, Orthopedics and Sports Medicine

View Paper: https://www.semanticscholar.org/paper/33ca680e4dd214dd5ce77eba62534b652c4028a8

Citations in the corpus

• 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the preventionof sudden cardiac death (2015, neutral): “The histological hallmark of the disease is replacement of cardiomyocytes by adipose and fibrous tissue.(382,383) Clinically, ARVC is defined by structural and functional abnormalities of the right ventricle, but LV involvement occurs in .”
• Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria. (2010, neutral): “Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is predominantly a genetically determined heart muscle disorder that is characterized pathologically by fibrofatty replacement of the right ventricular (RV) myocardium.(1) In the early stage of the disease, structural changes may be ”