<p><b>A.</b> Basal electrocardiogram. <b>B.</b> Electrocardiogram after flecainide test, showing type I Brugada pattern. <b>C.</b> Family pedigree. The proband is indicated by an arrow. Subjects affected and unaffected by BrS are indicated by solid and open symbols, respectively. Genetic status for the <i>SCN5A</i> rearrangement is indicated by a superindex (+ or -).</p
Purpose Brugada syndrome (BrS) is a form of cardiac arrhythmia which may lead to sudden cardiac deat...
International audienceBACKGROUND: Mutations in SCN5A are identified in approximately 20% to 30% of p...
Brugada syndrome (BrS) is a rare genetic cardiac arrhythmia that can lead to sudden cardiac death in...
Mutations in SCN5A are identified in approximately 20% to 30% of probands affected by Brugada syndro...
BACKGROUND: Brugada syndrome (BrS) is associated with mutations in the cardiac sodium channel gene, ...
Brugada syndrome (BrS) is a form of cardiac arrhythmia which may lead to sudden cardiac death. The r...
Background: Brugada syndrome (BrS) is associated with mutations in the cardiac sodium channel gene, ...
Background: Brugada syndrome (BrS) is characterized by the type 1 Brugada ECG pattern. Pathogenic ra...
SCN5A gene variants are associated with both Brugada syndrome and conduction disturbances, sometime...
Mutations in the SCN5A gene are responsible for multiple phenotypical presentations including Brugad...
Brugada syndrome (BrS) is marked by an elevated ST-segment elevation and increased risk of sudden ca...
Background: Brugada syndrome (BrS) is characterized by the type 1 Brugada ECG pattern. Pathogenic ra...
SCN5A gene variants are associated with both Brugada syndrome and conduction disturbances, sometimes...
AbstractIn 1992, the Brugada syndrome (BrS) was recognized as a disease responsible for sudden cardi...
Background: The genetic architecture of Brugada syndrome (BrS) is emerging as an increasingly comple...
Purpose Brugada syndrome (BrS) is a form of cardiac arrhythmia which may lead to sudden cardiac deat...
International audienceBACKGROUND: Mutations in SCN5A are identified in approximately 20% to 30% of p...
Brugada syndrome (BrS) is a rare genetic cardiac arrhythmia that can lead to sudden cardiac death in...
Mutations in SCN5A are identified in approximately 20% to 30% of probands affected by Brugada syndro...
BACKGROUND: Brugada syndrome (BrS) is associated with mutations in the cardiac sodium channel gene, ...
Brugada syndrome (BrS) is a form of cardiac arrhythmia which may lead to sudden cardiac death. The r...
Background: Brugada syndrome (BrS) is associated with mutations in the cardiac sodium channel gene, ...
Background: Brugada syndrome (BrS) is characterized by the type 1 Brugada ECG pattern. Pathogenic ra...
SCN5A gene variants are associated with both Brugada syndrome and conduction disturbances, sometime...
Mutations in the SCN5A gene are responsible for multiple phenotypical presentations including Brugad...
Brugada syndrome (BrS) is marked by an elevated ST-segment elevation and increased risk of sudden ca...
Background: Brugada syndrome (BrS) is characterized by the type 1 Brugada ECG pattern. Pathogenic ra...
SCN5A gene variants are associated with both Brugada syndrome and conduction disturbances, sometimes...
AbstractIn 1992, the Brugada syndrome (BrS) was recognized as a disease responsible for sudden cardi...
Background: The genetic architecture of Brugada syndrome (BrS) is emerging as an increasingly comple...
Purpose Brugada syndrome (BrS) is a form of cardiac arrhythmia which may lead to sudden cardiac deat...
International audienceBACKGROUND: Mutations in SCN5A are identified in approximately 20% to 30% of p...
Brugada syndrome (BrS) is a rare genetic cardiac arrhythmia that can lead to sudden cardiac death in...