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…rs). The cohort included 100 HCM, 41 DCM, and 39 arrhythmogenic cardiomyopathy (ACM) cases. Ethnic distribution was 49% White, 10.6% Black, 10…

…on Genetic testing is increasingly central to the management of dilated cardiomyopathy (DCM), enabling cascade screening and refining diagnosis and pr…

…Dilated cardiomyopathy (DCM) has an estimated prevalence of 1 in 200 in the UK and is …

… cardiac conditions, including dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM), may have a monogenic cause identified through genetic te…

…Conclusion The TRED-HF2 trial enrolled a contemporary recovered DCM population with substantially higher baseline GDMT optimisation…

…terise the myocardial transcriptomic landscape of patients with systemic sclerosis (SSc) with primary heart involvement (pHI) and identify molecul…

…Dilated cardiomyopathy (DCM) has an estimated prevalence of 1 in 250 in the UK and is …

…yopathy). No patient fulfilled arrhythmogenic right ventricular cardiomyopathy (ARVC) criteria. Most TTNtv were located on the A-band (74%). M…

…ct of neuromuscular symptoms after HTx.Results 40 patients with laminopathy underwent HTx (median age 45.4 years, 57.5% males). HTx followe…

…(SCD) remain leading contributors to mortality in patients with dilated cardiomyopathy (DCM). Understanding the incidence of these events and identify…

…Background Dilated cardiomyopathy (DCM) is a progressive myocardial disease characterized by vent…

…stics and management plans are generalised across all causes of DCM, natural history and response to therapy may vary depending on …