Add to ORKGBrugada syndrome is electrocardiographically characterised by ST segment elevation in right precordial leads and the occurrence of episodes of polymorphic ventricular tachycardia. It is also associated with a high risk of sudden death, which may be the first manifestation of the disease. Various mutations of SCN5A gene encoding for the cardiac sodium channel are among the proven causes of BS. ICD remains the only treatment for BS of proven efficacy. However, many questions about etiology, underlying mechanisms, safety of asymptomatic patients and treatment options for BS remain unanswered. (Cardiol J 2007; 14: 429-435
History of present illness: A 56-year-old male, with a history of hypertension, diabetes, and dysli...
Brugada syndrome is a heterogeneous genetic channelopathy that predisposes to ventricular arrhythmia...
AbstractThe Brugada syndrome (BrS) and the long QT syndrome are the most frequently diagnosed geneti...
Brugada syndrome is electrocardiographically characterised by ST segment elevation in right precordi...
Brugada syndrome is electrocardiographically characterised by ST segment elevation in right precordi...
Brugada syndrome (BrS) is a rare disease, caused by mutations in the gene that encodes cardiac sodiu...
Brugada Syndrome was initially described by Brugada brothers in their seminal paper published in the...
This chapter describes the epidemiology, ECG pattern, genetic and molecular bases, clinical manifest...
In 1992, Brugada and Brugada described 8 patients with a history of aborted sudden death and a disti...
Abstract A novel clinical entity characterized by ST segment elevation in right precordial leads (V1...
Brugada Syndrome (BrS) is an autosomal dominant channelopathy with variable penetrance affecting the...
Brugada syndrome (BrS) is an inherited ion channel channelopathy predisposing to ventricular arrhyth...
More than three decades since its initial description in 1993, Brugada syndrome remains engulfed in ...
We report on a youngster followed by his paediatrician from birth until 14 years of age for prematur...
First presented by Brugada and Brugada in 1992, Brugada Syndrome (BrS) is a primary electrical disea...
History of present illness: A 56-year-old male, with a history of hypertension, diabetes, and dysli...
Brugada syndrome is a heterogeneous genetic channelopathy that predisposes to ventricular arrhythmia...
AbstractThe Brugada syndrome (BrS) and the long QT syndrome are the most frequently diagnosed geneti...
Brugada syndrome is electrocardiographically characterised by ST segment elevation in right precordi...
Brugada syndrome is electrocardiographically characterised by ST segment elevation in right precordi...
Brugada syndrome (BrS) is a rare disease, caused by mutations in the gene that encodes cardiac sodiu...
Brugada Syndrome was initially described by Brugada brothers in their seminal paper published in the...
This chapter describes the epidemiology, ECG pattern, genetic and molecular bases, clinical manifest...
In 1992, Brugada and Brugada described 8 patients with a history of aborted sudden death and a disti...
Abstract A novel clinical entity characterized by ST segment elevation in right precordial leads (V1...
Brugada Syndrome (BrS) is an autosomal dominant channelopathy with variable penetrance affecting the...
Brugada syndrome (BrS) is an inherited ion channel channelopathy predisposing to ventricular arrhyth...
More than three decades since its initial description in 1993, Brugada syndrome remains engulfed in ...
We report on a youngster followed by his paediatrician from birth until 14 years of age for prematur...
First presented by Brugada and Brugada in 1992, Brugada Syndrome (BrS) is a primary electrical disea...
History of present illness: A 56-year-old male, with a history of hypertension, diabetes, and dysli...
Brugada syndrome is a heterogeneous genetic channelopathy that predisposes to ventricular arrhythmia...
AbstractThe Brugada syndrome (BrS) and the long QT syndrome are the most frequently diagnosed geneti...
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