Brugada syndrome (BrS) is a rare hereditary arrhythmia disorder, with a distinctive ECG
pattern, correlated with an increased risk of ventricular arrhythmias and sudden cardiac …

Brugada syndrome (BrS) is an inherited cardiac disorder, characterised by a typical ECG
pattern and an increased risk of arrhythmias and sudden cardiac death (SCD). BrS is a …

Brugada syndrome (BrS) is an inherited cardiac arrhythmic disorder that can lead to sudden
death, with a prevalence of 1: 5000 in Caucasian population and affecting mainly male …

Brugada syndrome (BrS) is an inherited cardiac arrhythmia syndrome that causes a
heightened risk for ventricular tachyarrhythmias and sudden cardiac death. BrS is …

For the last 10 years, applying new sequencing technologies to thousands of whole exomes
has revealed the high variability of the human genome. Extreme caution should thus be …

Brugada syndrome (BrS) is an inherited electrical heart disease associated with a high risk
of sudden cardiac death (SCD). The genetic characterization of BrS has always been …

Brugada syndrome is a heritable channelopathy characterized by a peculiar
electrocardiogram (ECG) pattern and increased risk of cardiac arrhythmias and sudden …

Brugada syndrome (BrS) is a clinical entity first described in 1992. BrS is characterized by
ST-segment elevations in the right precordial leads and susceptibility to ventricular …

Brugada syndrome (BrS) is an inherited cardiac channelopathy first diagnosed in 1992 but
still considered a challenging disease in terms of diagnosis, arrhythmia risk prediction …

Brugada syndrome (BrS) is diagnosed by a coved-type ST-segment elevation in the right
precordial leads on the electrocardiogram (ECG), and it is associated with an increased risk …