Empiric quinidine therapy for asymptomatic Brugada syndrome: time for a prospective registry.
作者信息
Viskin Sami, Wilde Arthur A M, Tan Hanno L, Antzelevitch Charles, Shimizu Wataru, Belhassen Bernard
机构信息
Tel-Aviv Sourasky Medical Center, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
出版信息
Heart Rhythm. 2009 Mar;6(3):401-4. doi: 10.1016/j.hrthm.2008.11.030. Epub 2008 Dec 3.
Abstract
摘要
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Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans.与人类Brugada综合征和心脏传导疾病相关的钠通道β1亚基突变。
J Clin Invest. 2008 Jun;118(6):2260-8. doi: 10.1172/JCI33891.
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Atrial fibrillation in patients with Brugada syndrome relationships of gene mutation, electrophysiology, and clinical backgrounds.Brugada综合征患者的心房颤动：基因突变、电生理学与临床背景的关系
J Am Coll Cardiol. 2008 Mar 25;51(12):1169-75. doi: 10.1016/j.jacc.2007.10.060.
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Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias.甘油-3-磷酸脱氢酶1样基因（GPD1-L）突变会降低心脏钠离子电流并导致遗传性心律失常。
Circulation. 2007 Nov 13;116(20):2260-8. doi: 10.1161/CIRCULATIONAHA.107.703330. Epub 2007 Oct 29.
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Role of programmed ventricular stimulation in patients with Brugada syndrome: a meta-analysis of worldwide published data.程控心室刺激在Brugada综合征患者中的作用：全球已发表数据的荟萃分析。
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