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Brugada Syndrome (disorder)

Known as: BRUGADA SYNDROME 1, RIGHT BUNDLE BRANCH BLOCK, ST SEGMENT ELEVATION, AND SUDDEN DEATH SYNDROME, Brugada Syndrome Ventricular Arrhythmia 
An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling… 
National Institutes of Health

Related topics

Related topics

18 relations
Autosomal dominant inheritanceCardiac ArrestClinical Data Interchange Standards Consortium TerminologyIn Blood

Narrower (5)

Brugada Syndrome 3Brugada Syndrome 8CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)Conduction disorder of the heart

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Missense Mutations in Plakophilin-2 Cause Sodium Current Deficit and Associate With a Brugada Syndrome Phenotype
Background— Brugada syndrome (BrS) primarily associates with the loss of sodium channel function. Previous studies showed… 
Review
2013
Review
2013
Impact of genetics on the clinical management of channelopathies.
Highly Cited
2010
Highly Cited
2010
The pathophysiological mechanism underlying Brugada syndrome: depolarization versus repolarization.
Review
2009
Review
2009
Sodium channel mutations and arrhythmias
Since the identification of the first SCN5A mutation associated with long QT syndrome in 1995, several mutations in this gene for… 
Highly Cited
2008
Highly Cited
2008
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans.
Brugada syndrome is a genetic disease associated with sudden cardiac death that is characterized by ventricular fibrillation and… 
Highly Cited
2008
Highly Cited
2008
Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome
Background— The Brugada syndrome, an inherited syndrome associated with a high incidence of sudden cardiac arrest, has been… 
Highly Cited
2007
Highly Cited
2007
Does Tpeak-Tend provide an index of transmural dispersion of repolarization?
Review
2005
Review
2005
Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more?
Highly Cited
2004
Highly Cited
2004
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic…
Highly Cited
1999
Highly Cited
1999
The circadian pattern of the development of ventricular fibrillation in patients with Brugada syndrome.
AIMS Brugada syndrome is considered to be a distinctive subgroup of idiopathic ventricular fibrillation. Identification of the… 
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