Brugada syndrome (BrS) is a hereditable syndrome, first reported in 1992, characterized by
right bundle branch block and an uncommon form of ST-T wave elevation in the V1 and V2 …

Brugada syndrome is electrocardiographically characterised by ST segment elevation in
right precordial leads and the occurrence of episodes of polymorphic ventricular …

The Brugada syndrome is an inherited cardiac disorder initially described in 1992 by Pedro
and Josep Brugada, with variable electrocardiographic features characteristic of right bundle …

In 1992, the Brugada brothers published a patient series of aborted sudden death, who were
successfully resuscitated from ventricular fibrillation (VF). These patients had a characteristic …

The authors present current opinion on diagnosis and treatment of Brugada syndrome (BS).
Recent studies have shown that BS is associated with a high risk of sudden cardiac death …

Brugada syndrome (BrS) is a cardiac channelopathy associated with ventricular arrhythmias
and sudden cardiac death. Diagnosis of BrS is based on type 1 BrS electrocardiogram …

Brugada syndrome is a rare cardiac arrhythmia characterized by electrocardiographic right
bundle branch block and persistent ST-segment elevation in the right precordial leads. It is …

Abstract In 1992, the Brugada syndrome (BrS) was recognized as a disease responsible for
sudden cardiac death, characterized by a right bundle-branch block with ST segment …

Brugada syndrome (BrS) is an autosomal-dominant condition mainly caused by defects in
sodium channels causing ST-segment elevation in electrocardiograms (ECGs) in the V1 and …

The Brugada syndrome (BS) is a hereditary disease characterized by typical
electrocardiographic alterations (elevation of the ST segment in right precordial leads) that …