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Cited by 303

The DOI matches its Crossref record; 140 of the 140 references it cites were found in a registry or an index.

Brugada Syndrome

Open access
ANTZELEVITCH, CHARLES·2006·Pacing and Clinical Electrophysiology

Abstract

First introduced as a new clinical entity in 1992, the Brugada syndrome is associated with a relatively high risk of sudden death in young adults, and occasionally in children and infants. Recent years have witnessed a striking proliferation of papers dealing with the clinical and basic aspects of the disease. Characterized by a coved‐type ST‐segment elevation in the right precordial leads of the electrocardiogram (ECG), the Brugada syndrome has a genetic basis that thus far has been linked only to mutations in SCN5A, the gene that encodes the α‐subunit of the sodium channel. The Brugada ECG is often concealed, but can be unmasked or modulated by a number of drugs and pathophysiological states including sodium channel blockers, a febrile state, vagotonic agents, tricyclic antidepressants, as well as cocaine and propranolol intoxication. Average age at the time of initial diagnosis or sudden death is 40 ± 22, with the youngest patient diagnosed at 2 days of age and the oldest at 84 years. This review provides an overview of the clinical, genetic, molecular, and cellular aspects of the Brugada syndrome, incorporating the results of two recent consensus conferences. Controversies with regard to risk stratification and newly proposed pharmacologic strategies are discussed.

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Metadata

Authors
ANTZELEVITCH, C.
Venue
Pacing and Clinical Electrophysiology
Publisher
Wiley
Published
2006-10
Volume
29
Issue
10
Pages
1130-1159
ISSN
  • 0147-8389 (ISSN-L)
  • 1540-8159
OpenAlex
W4210965788
Cited by
303
References
140
FWCI
14.22
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Brugada Syndrome. https://app.cochat.ai/papers/10.1111/j.1540-8159.2006.00507.x
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ANTZELEVITCH, C. (2006). Brugada Syndrome. Pacing and Clinical Electrophysiology. https://doi.org/10.1111/j.1540-8159.2006.00507.x

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