Biomarkers in inherited arrhythmias: necessity for validation and collaboration

被引：1

作者：

Wilde, Arthur A. M. ^{[1
]}

Lodder, Elisabeth M. ^{[1
]}

机构：

[1] Univ Amsterdam, Acad Univ Med Ctr, Dept Clin & Expt Cardiol, Ctr Heart,Locat AMC, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands

来源：

EUROPEAN HEART JOURNAL | 2020年 / 41卷 / 47期

关键词：

BRUGADA SYNDROME;

D O I：

10.1093/eurheartj/ehaa708

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

This commentary refers to 'Biomarkers in inherited arrhythmias: opportunities for validation and collaboration', by R.M. Hamilton et al., on pages 4521-4522.

引用

页码：4523 / 4524

页数：2

共 4 条

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Hamilton, Robert M. ;

Chatterjee, Diptendu ;

Saguner, Ardan M. .

EUROPEAN HEART JOURNAL, 2020, 41 (47) :4521-4522

[3] A highly specific biomarker for Brugada syndrome. Also too good to be true? [J].

Wilde, Arthur A. M. ;

Lodder, Elisabeth M. .

EUROPEAN HEART JOURNAL, 2020, 41 (30) :2891-2893

[4] Clinical Spectrum of SCN5A Mutations Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy [J].

Wilde, Arthur A. M. ;

Amin, Ahmad S. .

JACC-CLINICAL ELECTROPHYSIOLOGY, 2018, 4 (05) :569-579

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