Introduction: Brugada syndrome (BrS) is an autosomal dominant genetic disorder involving the abnormal function of cardiac voltage-gated sodium ion channels. Sodium channel loss of function can lead to early repolarization and loss of the Phase 2 action potential dome in cardiomyocytes. In BrS, this sodium channelopathy occurs in some, but not all, epicardial cells thus creating 1) juxtaposition of depolarized and repolarized cells in the epicardium and 2) a transmural voltage gradient. Together, these conditions can set up a Phase 2 reentry and resultant malignant cardiac arrhythmia. Of the three types of electrocardiogram (EKG) changes seen in BrS, only the Type 1 EKG is considered diagnostic. In a controlled setting, sodium channel blocke...
Introduction: The vast majority of cases of sudden cardiac arrest (SCA) are caused by ventricular t...
After the first description of Brugada syndrome [1] and its genetic mutation in SCN5A gene [2], the...
Abstract: Brugada syndrome is an inherited arrhythmogenic disorder that exhibits ECG ST-segment elev...
INTRODUCTION: Brugada syndrome (BrS) is an autosomal dominant genetic disorder involving the abnorma...
Introduction: Brugada syndrome (BrS) is an autosomal dominant genetic disorder involving the abnorma...
Introduction. Brugada syndrome is an arrhythmogenic disease characterized by coved ST segment eleva...
In 1992, Brugada et al 1 suggested that the presence of right bundle-branch block and ST-segment ele...
Brugada syndrome (BrS) is an "inherited" condition characterized by predisposition to syncope and ca...
Brugada syndrome is electrocardiographically characterised by ST segment elevation in right precordi...
As a clinical entity the Brugada syndrome has existed since 1992 and has been associated with a high...
Brugada syndrome is electrocardiographically characterised by ST segment elevation in right precordi...
Brugada Syndrome (BrS) is a channelopathy caused partially by mutations in the cardiac sodium channe...
Brugada syndrome is a congenital channelopathy in cardiac ion transmembrane causing an alteration in...
Introduction: Brugada Syndrome is a cardiac ion channel disorder that affects the sodium current. Th...
BACKGROUND: The role of structural heart disease and sodium channel dysfunction in the induction of ...
Introduction: The vast majority of cases of sudden cardiac arrest (SCA) are caused by ventricular t...
After the first description of Brugada syndrome [1] and its genetic mutation in SCN5A gene [2], the...
Abstract: Brugada syndrome is an inherited arrhythmogenic disorder that exhibits ECG ST-segment elev...
INTRODUCTION: Brugada syndrome (BrS) is an autosomal dominant genetic disorder involving the abnorma...
Introduction: Brugada syndrome (BrS) is an autosomal dominant genetic disorder involving the abnorma...
Introduction. Brugada syndrome is an arrhythmogenic disease characterized by coved ST segment eleva...
In 1992, Brugada et al 1 suggested that the presence of right bundle-branch block and ST-segment ele...
Brugada syndrome (BrS) is an "inherited" condition characterized by predisposition to syncope and ca...
Brugada syndrome is electrocardiographically characterised by ST segment elevation in right precordi...
As a clinical entity the Brugada syndrome has existed since 1992 and has been associated with a high...
Brugada syndrome is electrocardiographically characterised by ST segment elevation in right precordi...
Brugada Syndrome (BrS) is a channelopathy caused partially by mutations in the cardiac sodium channe...
Brugada syndrome is a congenital channelopathy in cardiac ion transmembrane causing an alteration in...
Introduction: Brugada Syndrome is a cardiac ion channel disorder that affects the sodium current. Th...
BACKGROUND: The role of structural heart disease and sodium channel dysfunction in the induction of ...
Introduction: The vast majority of cases of sudden cardiac arrest (SCA) are caused by ventricular t...
After the first description of Brugada syndrome [1] and its genetic mutation in SCN5A gene [2], the...
Abstract: Brugada syndrome is an inherited arrhythmogenic disorder that exhibits ECG ST-segment elev...