classified as an inherited channelopathy and has been linked to mutations in the SCN5A
gene that encodes the alpha subunit of the cardiac sodium channel (1). Patients with BrS …

The Brugada syndrome is an arrhythmic syndrome characterized by a right bundle branch
block pattern and ST segment elevation in the right precordial leads of the …

The Brugada syndrome was first described in 1992, and constitutes a new and distinct
clinical entity outlined by characteristic electrocardiograms (ECGs) and an associated high …

The Brugada syndrome describes a subgroup of patients at risk for the occurrence of
ventricular fibrillation who have no definable structural heart disease associated with a right …

An intriguing new clinical entity characterized by ST-segment elevation in the right
precordial electrocardiographic leads and a high incidence of sudden death in individuals …

Brugada syndrome is an example of a channelopathy caused by an alteration in the
transmembrane ion currents that together constitute the cardiac action potential …

We describe a 45-year-old Taiwanese man with specific features of Brugada syndrome but
no clinical features of structural heart disease. He was successfully treated with an …

Brugada Syndrome and Supraventricular Tachyarrhythmias. Introduction: The Brugada
syndrome is a distinct form of idiopathic ventricular fibrillation characterized by a unique …

The Brugada syndrome is an inherited channelopathy that alters the main transmembrane
ion currents that constitute the cardiac action potential. These changes not only modify the …

Idiopathic ventricular fibrillation in patients with an electrocardiogram (ECG) pattern of right
bundle branch block and ST-segment elevation in leads V1 to V3 (now frequently called …