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Brugada综合征

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作者 王鼎铁
出处 《中国急救医学》 CAS CSCD 北大核心 2004年第6期428-429,共2页 Chinese Journal of Critical Care Medicine
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参考文献10

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  • 2[2]Chen Q, Kirsch GE, Zhang D, et al . Genetic basis and molecular mechanisms for idiopathic ventricular fibrillation[ J]. Nature, 1998,392:293 - 296.
  • 3[3]BezzinaR,VeldampMV,VandenBergMP, etal .AsingleNa+ channel mutation causing both long - QT and Brugada syndromes [ J]. Circ Res,1999,85:1206- 1213.
  • 4[4]Weiss R, Barmada MM, Nguyen T, et al . Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3 [J]. Circulation,2002,105:707 - 713.
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  • 6[6]Wilde AA, Antzelevitch C, Borggrefe M, et al .Study group on the molecular basis of arrhythmias of the european society of cardiology.proposed diagnostic criteria for the Brugada syndrome [ J ]. Eur Heart J,2002,23(21 ): 1648 - 1654.
  • 7[7]Brugada J, Brugada R, Antzelevitch R, et al .Long - term follow - up individuals with the electrocardiographic pattern of right bundle - branch block and ST - segment elevation in precordial leads V1 to V3 [ J ] .Circulation, 2002,105 ( 1 ): 73 - 78.
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