Prevalence of Atrial Fibrillation in Patients with Brugada Syndrome in Taiwan. - Wikidata - wikimedia - TriplyDB

Prevalence of Atrial Fibrillation in Patients with Brugada Syndrome in Taiwan.

Prevalence of Atrial Fibrillation in Patients with Brugada Syndrome in Taiwan.

http://www.wikidata.org/entity/Q33167104

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Prevalence of Atrial Fibrillation in Patients with Brugada Syndrome in Taiwan.

http://www.wikidata.org/entity/Q33167104

description

2013 nî lūn-bûn

@nan

2013 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Prevalence of Atrial Fibrillation in Patients with Brugada Syndrome in Taiwan.

@ast

Prevalence of Atrial Fibrillation in Patients with Brugada Syndrome in Taiwan.

@en

type

label

Prevalence of Atrial Fibrillation in Patients with Brugada Syndrome in Taiwan.

@ast

Prevalence of Atrial Fibrillation in Patients with Brugada Syndrome in Taiwan.

@en

prefLabel

Prevalence of Atrial Fibrillation in Patients with Brugada Syndrome in Taiwan.

@ast

Prevalence of Atrial Fibrillation in Patients with Brugada Syndrome in Taiwan.

@en

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Acta Cardiologica Sinica

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Prevalence of Atrial Fibrillation in Patients with Brugada Syndrome in Taiwan.

@en

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Chia-Ti Tsai

http://www.w3.org/2001/XMLSchema#string

Ching-Yu Chen

http://www.w3.org/2001/XMLSchema#string

Jiunn-Lee Lin

http://www.w3.org/2001/XMLSchema#string

Jyh-Ming Jimmy Juang

http://www.w3.org/2001/XMLSchema#string

Lian-Yu Lin

http://www.w3.org/2001/XMLSchema#string

Ling-Ping Lai

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Wen-Jone Chen

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Yen-Bin Liu

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P2860

Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome

Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

"Brugada" syndrome: clinical data and suggested pathophysiological mechanism.

Assessment of noninvasive markers in identifying patients at risk in the Brugada syndrome: insight into risk stratification.

Arrhythmias in patients with Brugada-type electrocardiographic findings.

Spontaneous T wave alternans and premature ventricular contractions during febrile illness in a patient with Brugada syndrome.

Proposed diagnostic criteria for the Brugada syndrome: consensus report.

Clinical characteristics of Brugada syndrome in a Korean population.

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311-316

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scholarly article

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4

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2013-07-01T00:00:00Z

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27122723

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Brugada syndrome

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4804896

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