The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance

Published:2016-04-25 Issue: Volume:3 Page:
ISSN:2297-055X
Container-title:Frontiers in Cardiovascular Medicine
language:
Short-container-title:Front. Cardiovasc. Med.

Author:

Gourraud Jean-Baptiste,Barc Julien,Thollet Aurélie,Le Scouarnec Solena,Le Marec Hervé,Schott Jean-Jacques,Redon Richard,Probst Vincent

Publisher

Frontiers Media SA

Subject

Cardiology and Cardiovascular Medicine

Reference105 articles.

1. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome: a multicenter report;Brugada;J Am Coll Cardiol,1992

2. Brugada syndrome – an under-recognized electrical disease in patients with sudden cardiac death;Juang;Cardiology,2004

3. Sudden cardiac death with autopsy findings of uncertain significance: potential for erroneous interpretation;Papadakis;Circ Arrhythm Electrophysiol,2013

4. Proposed diagnostic criteria for the Brugada syndrome: consensus report;Wilde;Circulation,2002

5. Brugada syndrome: report of the second consensus conference endorsed by the Heart Rhythm Society and the European Heart Rhythm Association;Antzelevitch;Circulation,2005

Cited by 48 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Loss of sodium current caused by a Brugada syndrome–associated variant is determined by patient-specific genetic background;Heart Rhythm;2023-11

2. Noncoding RNAs and Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes in Cardiac Arrhythmic Brugada Syndrome;Cells;2023-10-03

3. Case report: State-of-the-art risk-modifying treatment of sudden cardiac death in an asymptomatic patient with a mutation in the SCN5A gene and a review of the literature;Frontiers in Cardiovascular Medicine;2023-09-06

4. HiPSC-derived cardiomyocyte to model Brugada syndrome: both asymptomatic and symptomatic mutation carriers reveal increased arrhythmogenicity;BMC Cardiovascular Disorders;2023-04-25

5. A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico Analysis;Genes;2023-02-08

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3