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Recurrent exercise-induced ventricular tachycardia in a patient with Brugada syndrome.

作者信息

Powers Edward M, Ashwath Mahi, London Barry, Mazur Alexander

机构信息

Division of Cardiovascular Medicine and Abboud Cardiovascular Research Center, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

出版信息

HeartRhythm Case Rep. 2020 Dec 5;7(3):144-147. doi: 10.1016/j.hrcr.2020.11.020. eCollection 2021 Mar.

DOI:10.1016/j.hrcr.2020.11.020
PMID:33786307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7987899/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5c/7987899/646401ccbf21/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5c/7987899/d5de94d87807/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5c/7987899/b2cfb6dff1c1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5c/7987899/646401ccbf21/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5c/7987899/d5de94d87807/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5c/7987899/b2cfb6dff1c1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5c/7987899/646401ccbf21/gr3.jpg

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本文引用的文献

1
Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.揭示致心律失常性右室心肌病与 Brugada 综合征的分子关联。
Nat Rev Cardiol. 2017 Dec;14(12):744-756. doi: 10.1038/nrcardio.2017.103. Epub 2017 Jul 13.
2
Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis.致心律失常性右室发育不良/心肌病中SCN5A突变的多层次分析提示疾病发病机制的非典型机制。
Cardiovasc Res. 2017 Jan;113(1):102-111. doi: 10.1093/cvr/cvw234.
3
Late gadolinium enhancement in Brugada syndrome: A marker for subtle underlying cardiomyopathy?
Brugada综合征的延迟钆增强：隐匿性潜在心肌病的一个标志物？
Heart Rhythm. 2017 Apr;14(4):583-589. doi: 10.1016/j.hrthm.2016.12.004. Epub 2016 Dec 3.
4
Relationship Between Arrhythmogenic Right Ventricular Cardiomyopathy and Brugada Syndrome: New Insights From Molecular Biology and Clinical Implications.致心律失常性右室心肌病与Brugada综合征的关系：分子生物学新见解及临床意义
Circ Arrhythm Electrophysiol. 2016 Apr;9(4):e003631. doi: 10.1161/CIRCEP.115.003631.
5
The role of mutations in the SCN5A gene in cardiomyopathies.SCN5A基因中的突变在心肌病中的作用。
Biochim Biophys Acta. 2016 Jul;1863(7 Pt B):1799-805. doi: 10.1016/j.bbamcr.2016.02.014. Epub 2016 Feb 23.
6
Monomorphic ventricular tachycardia in patients with Brugada syndrome: A multicenter retrospective study.Brugada 综合征患者的单形性室性心动过速：一项多中心回顾性研究。
Heart Rhythm. 2016 Mar;13(3):669-82. doi: 10.1016/j.hrthm.2015.10.038. Epub 2015 Oct 29.
7
Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome.布加综合征中的纤维化、连接蛋白43与传导异常
J Am Coll Cardiol. 2015 Nov 3;66(18):1976-1986. doi: 10.1016/j.jacc.2015.08.862.
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Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statement.致心律失常性右室心肌病/发育异常的治疗：一项国际特别工作组共识声明
Eur Heart J. 2015 Dec 7;36(46):3227-37. doi: 10.1093/eurheartj/ehv162. Epub 2015 Jul 27.
9
Desmosomes and the sodium channel complex: implications for arrhythmogenic cardiomyopathy and Brugada syndrome.桥粒与钠通道复合物：对致心律失常性心肌病和Brugada综合征的影响。
Trends Cardiovasc Med. 2014 Jul;24(5):184-90. doi: 10.1016/j.tcm.2014.02.001. Epub 2014 Feb 22.
10
Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.执行摘要：HRS/EHRA/APHRS关于遗传性原发性心律失常综合征患者诊断与管理的专家共识声明。
Heart Rhythm. 2013 Dec;10(12):e85-108. doi: 10.1016/j.hrthm.2013.07.021. Epub 2013 Jul 31.