The Brugada syndrome: clinical, genetic, cellular, and molecular abnormalities (Q34245293)

31 July 2017

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title

The Brugada syndrome: clinical, genetic, cellular, and molecular abnormalities (English)

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31 July 2017

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Naccarelli GV

1

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31 July 2017

Antzelevitch C

series ordinal

2

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31 July 2017

language of work or name

English

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publication date

1 May 2001

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American Journal of Medicine

31 July 2017

published in

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31 July 2017

volume

110

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31 July 2017

issue

7

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31 July 2017

page(s)

573-581

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Unfavorable outcome in patients with primary electrical disease who survived an episode of ventricular fibrillation

31 July 2017

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Cardiac conduction defects associate with mutations in SCN5A

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Functional suppression of sodium channels by beta(1)-subunits as a molecular mechanism of idiopathic ventricular fibrillation

7 January 2021

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Cellular basis for the electrocardiographic J wave

7 January 2021

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Cellular basis for the Brugada syndrome and other mechanisms of arrhythmogenesis associated with ST-segment elevation

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7 January 2021

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7 January 2021

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Effects of electrophysiologic-guided therapy with Class IA antiarrhythmic drugs on the long-term outcome of patients with idiopathic ventricular fibrillation with or without the Brugada syndrome

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Sudden death in high-risk family members: Brugada syndrome

7 January 2021

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Mode of onset of ventricular fibrillation in patients with Brugada syndrome detected by implantable cardioverter defibrillator therapy

7 January 2021

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10.1016/S0002-9343(01)00625-8

7 January 2021

Identifiers

DOI

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31 July 2017

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