Background Arrhythmogenic right ventricular cardiomyopathy (ARVC) is predominantly caused by desmosomal genetic variants, and clinical hallmarks include arrhythmias and systolic dysfunction. We aimed ...

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Figure 2. Risk factors for right ventricular failure after LVAD implantation not related to the intrinsic right ventricular function. LVEDD, left ventricular end-diastolic diameter; NICM, non-ischemic ...

Background Regular intensive physical activity is associated with non-pathological changes in cardiac morphology. Differential diagnosis with arrhythmogenic right ventricular cardiomyopathy (ARVC) ...

Abbreviations: ARVD/C, arrhythmogenic right ventricular dysplasia/cardiomyopathy; VT, ventricular tachycardia. Author's Contributions: P Petrakopoulou and M Greif contributed equally to the ...

Hypertrophic cardiomyopathy (HCM ... 6-11); and a normal right ventricle. The cardiac catheterization revealed a mean right atrial pressure of 5 mm Hg (normal, 2-6); a right ventricular systolic ...

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Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disease ... beam alignment and correct orientation are essential to prevent WT overestimation or foreshortening and caution ...

In the past decade there has been a growing interest in understanding sex and gender differences in myocarditis and dilated cardiomyopathy ... ventricular assist devices (VADs) used in 11 patients (6 ...

These findings were specific for hydroxychloroquine-induced cardiomyopathy. This case highlights the importance of clinical ... mild to moderate mitral regurgitation, moderate right ventricular ...

DESIGN Detailed macroscopic and histological examination at 19 segments of the left and right ventricle and the left atrial free wall. PATIENTS 72 patients with hypertrophic cardiomyopathy who had ...

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 ...