You have full access to this article via your institution. The development of systolic dysfunction in patients with HCM has serious clinical implications because it is associated with high rates ...

BACKGROUND: Penetrance and risk of ventricular arrhythmias (VAs) in arrhythmogenic right ventricular cardiomyopathy (ARVC) are increasingly recognized as being genotype specific. Therefore, ...

But it’s critical for new moms to keep an eye out for signs of postpartum complications because in rare cases, a serious form of heart disease known as peripartum cardiomyopathy (PPCM) can develop ...

This guide will help you understand how HCM presents in children and how to support your child through diagnosis and treatment.

Abstract: In this paper, a new piecewise modeling for approximation of ECG signal is presented. Most of the modeling methods are focused to obtain the best approximation of the entire ECG signal. The ...

Two major UK cardiology trials are falling behind recruitment targets, prompting changes to entry criteria and calls for ...

Happy Heart Syndrome, a rare condition, mirrors broken heart syndrome but is triggered by intense joy. Overwhelming happiness ...

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 ...

Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiac condition ... Cardiac investigations aimed at monitoring the effects of exercise on the phenotype from a structural and electrical ...

Objective The AliveCor KardiaBand (KB) is an Food and Drug Administration-approved smartwatch-based cardiac rhythm monitor that records a lead-Intelligent ECG (iECG). Despite the appeal of wearable ...

Hypertrophic cardiomyopathy is a common yet under-recognized genetic structural heart condition characterized by left ventricular hypertrophy. Patients may present with obstructive disease ...