Differential diagnosis with arrhythmogenic right ventricular cardiomyopathy (ARVC) constitutes a frequent problem ... None of them presented a family history of ARVC and/or of juvenile sudden death ...

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

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

Results: 453 cases of sudden death from 1994 to 2003 (278 men (61.4% ... hypertrophic cardiomyopathy, dilated cardiomyopathy, and arrhythmogenic right ventricular dysplasia; (2) inflammatory disorders ...

With the increasing cases of sudden deaths during workouts, cardiologists have advised people planning to engage in an exercise to seek counsel from medical experts to ascertain their fitness to avoid ...

The researchers found that just six weeks of anabolic steroid use can harm the way cells in the heart work together. The steroids weaken the cell connections and reduce the function of sodium channels ...

South San Francisco, CA, January 30, 2025 – The California Institute for Regenerative Medicine (CIRM), one of the world’s largest institutions dedicated to regenerative medicine, has awarded nearly ...

Figure 3. Twelve-lead ECG tracing during stress test shows the typical aspect of bidirectional ventricular tachycardia characterized by 180° alternating QRS axis on a beat-to-beat basis, with a right ...

View all available purchase options and get full access to this article. Department of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University ...

Aim In the clinical setting of acute myocarditis, existing guidelines recommend refraining from moderate-intensity to high-intensity sports for 3–6 months, yet the extent to which these ...

delayed or incomplete penetrance in arrhythmogenic right ventricular cardiomyopathy (ARVC)), either due to a de novo mutation (relatively common in Marfan syndrome, frequent in 22q11 deletion syndrome ...

the leading cause of sudden cardiac death in young individuals. Dilated cardiomyopathy: Enlargement of the heart chambers. Arrhythmogenic cardiomyopathy: Predominantly affects the right ventricle.