In 1992, the manuscript “Right bundle branch block, persistent ST segment elevation and
sudden cardiac death: A distinct clinical and electrocardiographic syndrome” was published …

The syndrome of right bundle branch block, persistent ST-segment elevation, and sudden
cardiac death, today better known as the Brugada syndrome, was described in 1992 as a …

In 1986, two young brothers who survived documented cardiac arrests exhibited a specific
electrocardiographic pattern providing a link to sudden death. Similar observations in other …

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 …

Abstract [eng] In 1992, the Brugada brothers, Pedro and Josep, made a groundbreaking
discovery by describing a previously unknown clinical condition that exhibited distinctive …

A novel clinical entity characterized by ST segment elevation in right precordial leads (V1 to
V3), incomplete or complete right bundle branch block, and susceptibility to ventricular …

The Brugada syndrome (BrS) is an inherited channelopathy characterized by an elevated
ST segment or J wave appearing in the right precordial leads (V1–V3), often followed by a …

The syndrome of right bundle branch block (BBB), persistent ST-segment elevation, and
sudden cardiac death (from polymorphic ventricular tachycardia [PVT] or ventricular …

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 …

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 …