Brugada syndrome (BrS) is a primary electrical disease associated with life-threatening arrhythmias. It is estimated to cause at least 20% of sudden cardiac deaths (SCDs) in patients with normal cardiac anatomy. In this review paper, we discuss recent advances in complex BrS pathogenesis, diagnostics, and current standard approaches to major arrhythmic events (MAEs) risk stratification. Additionally, we describe a protocol for umbrella reviews to systematically investigate clinical, electrocardiographic, electrophysiological study, programmed ventricular stimulation, and genetic factors associated with BrS, and the risk of MAEs. Our evaluation will include MAEs such as sustained ventricular tachycardia, ventricular fibrillation, appropriate...
As a clinical entity the Brugada syndrome has existed since 1992 and has been associated with a high...
AbstractThe Brugada syndrome (BrS) is a malignant, genetically-determined, arrhythmic syndrome manif...
BACKGROUND: Treatment of patients with Brugada syndrome is complicated by the incomplete informati...
Brugada syndrome (BrS) is a primary electrical disease associated with life-threatening arrhythmias....
Brugada syndrome (BrS) is a primary electrical disease associated with life-threatening arrhythmias....
International audienceBrugada syndrome is a rare inherited arrhythmia syndrome leading to an increas...
International audienceBrugada syndrome is a rare inherited arrhythmia syndrome leading to an increas...
Brugada syndrome (BrS) is an inherited cardiac disorder, characterised by a typical ECG pattern and ...
Brugada syndrome is an inherited disease characterized by an increased risk of sudden cardiac death ...
Brugada syndrome is a congenital channelopathy in cardiac ion transmembrane causing an alteration in...
Brugada syndrome (BrS) is a rare hereditary arrhythmia disorder, with a distinctive ECG pattern, cor...
Brugada syndrome (BrS) was first described in 1992 as an aberrant pattern of ST segment elevation in...
Brugada syndrome (BrS) was first described in 1992 as an aberrant pattern of ST segment elevation in...
Brugada syndrome (BrS) was first described in 1992 as an aberrant pattern of ST segment elevation in...
Brugada syndrome (BrS) is an inherited ion channel channelopathy predisposing to ventricular arrhyth...
As a clinical entity the Brugada syndrome has existed since 1992 and has been associated with a high...
AbstractThe Brugada syndrome (BrS) is a malignant, genetically-determined, arrhythmic syndrome manif...
BACKGROUND: Treatment of patients with Brugada syndrome is complicated by the incomplete informati...
Brugada syndrome (BrS) is a primary electrical disease associated with life-threatening arrhythmias....
Brugada syndrome (BrS) is a primary electrical disease associated with life-threatening arrhythmias....
International audienceBrugada syndrome is a rare inherited arrhythmia syndrome leading to an increas...
International audienceBrugada syndrome is a rare inherited arrhythmia syndrome leading to an increas...
Brugada syndrome (BrS) is an inherited cardiac disorder, characterised by a typical ECG pattern and ...
Brugada syndrome is an inherited disease characterized by an increased risk of sudden cardiac death ...
Brugada syndrome is a congenital channelopathy in cardiac ion transmembrane causing an alteration in...
Brugada syndrome (BrS) is a rare hereditary arrhythmia disorder, with a distinctive ECG pattern, cor...
Brugada syndrome (BrS) was first described in 1992 as an aberrant pattern of ST segment elevation in...
Brugada syndrome (BrS) was first described in 1992 as an aberrant pattern of ST segment elevation in...
Brugada syndrome (BrS) was first described in 1992 as an aberrant pattern of ST segment elevation in...
Brugada syndrome (BrS) is an inherited ion channel channelopathy predisposing to ventricular arrhyth...
As a clinical entity the Brugada syndrome has existed since 1992 and has been associated with a high...
AbstractThe Brugada syndrome (BrS) is a malignant, genetically-determined, arrhythmic syndrome manif...
BACKGROUND: Treatment of patients with Brugada syndrome is complicated by the incomplete informati...