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… (More)
National Institutes of Health

Related topics

Related topics

16 relations
Autosomal dominant inheritanceCardiac ArrestClinical Data Interchange Standards Consortium TerminologyIn Blood
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Narrower (4)

Brugada Syndrome 8CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)Conduction disorder of the heartSudden unexpected nocturnal death syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances
Sudden cardiac death poses a unique challenge to clinicians because it may be the only symptom of an inherited heart condition… (More)
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Highly Cited
2010
Highly Cited
2010
Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry.
BACKGROUND Brugada syndrome is characterized by ST-segment elevation in the right precordial leads and an increased risk of… (More)
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Highly Cited
2010
Highly Cited
2010
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.
BACKGROUND Brugada syndrome (BrS) is a common heritable channelopathy. Mutations in the SCN5A-encoded sodium channel (BrS1… (More)
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Review
2005
Review
2005
Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.
Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed from being a rare disease to one that is… (More)
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Review
2005
Review
2005
Brugada syndrome: report of the second consensus conference.
Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed from being a rare disease to one that is… (More)
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Review
2002
Review
2002
Proposed diagnostic criteria for the Brugada syndrome: consensus report.
Asyndrome characterized by ST-segment elevation in right precordial leads (V1 to V3) that is unrelated to ischemia, electrolyte… (More)
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Highly Cited
2002
Highly Cited
2002
Natural history of Brugada syndrome: insights for risk stratification and management.
BACKGROUND Treatment of patients with Brugada syndrome is complicated by the incomplete information on the natural history of the… (More)
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Highly Cited
1999
Highly Cited
1999
Cellular basis for the Brugada syndrome and other mechanisms of arrhythmogenesis associated with ST-segment elevation.
BACKGROUND The Brugada syndrome is characterized by marked ST-segment elevation in the right precordial ECG leads and is… (More)
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Highly Cited
1999
Highly Cited
1999
A single Na(+) channel mutation causing both long-QT and Brugada syndromes.
Mutations in SCN5A, the gene encoding the cardiac Na(+) channel, have been identified in 2 distinct diseases associated with… (More)
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Highly Cited
1996
Highly Cited
1996
Autonomic and antiarrhythmic drug modulation of ST segment elevation in patients with Brugada syndrome.
OBJECTIVES We examined the modulatory effects of autonomic nervous system and antiarrhythmic drugs on the ST segment in patients… (More)
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