Brugada syndrome (BrS) is an inherited ion channel channelopathy predisposing to
ventricular arrhythmias and sudden cardiac death. Originally believed to be predominantly …

Abstract The management of Brugada Syndrome (BrS) patients at intermediate risk of
arrhythmic events remains controversial. The present study evaluated the predictive …

Objectives Brugada syndrome (BrS) is an ion channelopathy that predisposes affected
patients to spontaneous ventricular tachycardia/fibrillation (VT/VF) and sudden cardiac …

Introduction Long QT syndrome (LQTS) is a less prevalent cardiac ion channelopathy than
Brugada syndrome in Asia. The present study compared the outcomes between …

Background A combination of clinical and electrocardiographic risk factors is used for risk
stratification in Brugada syndrome. In this study, we tested the hypothesis that the …

Brugada syndrome (BrS) is a rare disorder characterized by coved or saddle-shaped ST-
segment elevation in the right precordial leads on the electrocardiogram. Risk stratification …

Background: Patients suffering from Brugada syndrome (BrS) are at an increased risk of life-
threatening ventricular arrhythmias. Whilst electrocardiographic (ECG) variables have been …

Abstract Long QT syndrome (LQTS), Brugada syndrome (BrS), and catecholaminergic
polymorphic ventricular tachycardia (CPVT) are genetic diseases of the heart caused by …

Brugada syndrome (BrS) is an arrhythmogenic disorder increasing the risk of syncopal
episodes and sudden cardiac death. BrS usually runs through families with reduced …

Abstract Background Brugada syndrome (BrS) is an inherited arrhythmic disease associated
with an increased risk of major arrhythmic events (MAE). Previous studies reported that a …