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钠通道疾病与心脏猝死 被引量:6

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出处 《中国心脏起搏与心电生理杂志》 2003年第3期161-165,共5页 Chinese Journal of Cardiac Pacing and Electrophysiology
基金 国家自然科学基金资助项目 (批准号 :3 0 170 3 81)
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参考文献18

  • 1BezzinaCR RookMB WildeAAM.Cardiac sodium channel and inherited arrhythmia syndromes[J].Cardiovascular Research,2001,49:257-257.
  • 2KyndtF ProbstV PotetF etal.Novel SCNSA mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family [J].Circulation,2001,104:3-3.
  • 3Balser JR. Sodium "channelopathies" and suuden death must you beso sensitive [ J ] ? Circulation Research, 1999,85 : 872.
  • 4Priori SG, Napolitano C, Giordano U,et al. Brugada syndrome and sudden cardiac death in children [ J ]. The Lancent,2000,355 : 808.
  • 5Wang Q, Li ZZ, Shen JX,et al. Genomic organization of the human SCN5A gene encoding the cardiac sodium channel [ J]. Genomics,1996,34:9.
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  • 7Wang DW, Viswanathan PC, Balser JR,et al . Clinical, genetic and biophysical characterization of SCN5A mutations associated with atrioventricular conduction block[ J]. Circulation,2002,105:341.
  • 8Akai J, Makita N,Sakurada H,et al . A novel SCNSA mutation associated with idiopathic ventricular fibrrilation without typical ECG findings of Brugada syndrome[ J]. FEBS,2000,479:29.
  • 9Schott JJ, Alshinawi C, Kyndt F, et al, Cardiac conduction defects associated with mutations in SCN5A[ J]. Nature Genetics, 1999,23:20.
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同被引文献74

  • 1李翠兰,胡大一,李运田,秦绪光,刘文玲,周金台,王吉云,李蕾,马志敏.76个长QT综合征先证者临床特征和治疗情况研究[J].中国心脏起搏与心电生理杂志,2004,18(6):414-418. 被引量:14
  • 2曾治宇,浦介麟,谭琛,滕思勇,陈剑虹,宿少勇,周晓阳,张澍,李一石,王方正,顾东风.心房颤动患者KCNQ1、KCNE1和KCNE4基因单核苷酸多态性研究[J].中华心血管病杂志,2005,33(11):987-991. 被引量:25
  • 3吴华,岳霞,陈新山.心脏钠通道SCN5A基因突变与致心律失常性疾病[J].中国法医学杂志,2005,20(6):344-346. 被引量:2
  • 4汪明慧,梁文同,沐贤友.长QT综合征的临床特点和治疗进展[J].国外医学(内科学分册),2006,33(1):4-6. 被引量:4
  • 5刘敬,陈自励.婴儿猝死综合征[J].中国当代儿科杂志,2007,9(1):85-89. 被引量:10
  • 6Tester D J, Kopplin LJ, Will ML, et al. Spectrum and prevalence of cardiac ryanodine receptor ( RyR2 ) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing. Heart Rhythm ,2005,2 : 1099-1105.
  • 7Schwartz PJ, Priori SG, Dumaine R, et al. A molecular link between the sudden infant death syndrome and the long-QT syndrome. N Engl J Med ,2000,343:262-267.
  • 8Moric-Janiszewska E, Herbert E, Cholewa K, et al. Mutational screening of SCN5A linked disorders in Polish patients and their familymembers. J Appl Genet ,2004,45:383-390.
  • 9Schwartz PJ, Priori SG, Bloise R, et al. Molecular diagnosis in a child with sudden infant death syndrome. Lancet ,2001,358 : 1342- 1343.
  • 10Kurokawa J, Abriel H, Kass RS. Molecular basis of the delayed rectifier current I(ks) in heart. J Mol Cell Cardiol,2001,33 :873-882.

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