参考文献
[1 ] Marban E. Cardiac channelopathies[J ] . Nature ,2002 ,415(6868) :213 - 218.
[2 ] Ackerman MJ . Cardiac channelopathies : It’s in the genes[J ] . Nat Med , 2004 ,10(5) :463 - 464.
[3 ] 李翠兰,胡大一. 离子通道病的种类和特点[J ] . 中国民康医学杂志,2005 ,17(2) : 76 - 80.
[ 4 ] Priori SG,Barhanin J ,Hauer RN ,et al. Genetic and molecular basis of Cardiac arrhythmias : Impact on clinical management (Parts 1 and II) [J ] . Circulation ,1999 ,99 (4) :518 - 528.
[5 ] Zhang L , Timothy KW ,Vincent GM, et al. Spectrum of ST2T2wave patterns and repolarization parameters in congenital long2QT syndrome : ECGfindings identify genotypes[J ] . Circulation ,2000 ,102(23) :2849 - 2855.
[6 ] Splawski I ,Timothy KW,Sharpe LM,et al. Ca(V) 1. 2 calcium channel dysfuncfion causes a multisystem disorder including arrhythmia and autism[J ] . Cell ,2004 ,119(1) :19- 31.
[7 ] Weiss R ,Barmada MM,Nguyen T,et al. Clinical and molecular heterogeneity in the Brugada syndrome : a novelgene locus on chromosome 3 [J ] . Circulation , 2002 ,105(6) :707 - 713.
[8 ] Marx SO ,Reilen S ,Hisamatsu Y,et al. PKA phosphorylation dissociates FKBP12. 6 from the calcium release channel ( ryanodine receptor) : Defective regulation in failing heart [J ] . Cell , 2000 ,101(4) :365 - 376.
[9 ] Viatchenko2Karpinski S ,Terentyev D ,Gyorke I ,et al. Abnormal calcium signaling and sudden cardiac death associated with mutation of ealsequestrin[J ] . Circ Res ,2004 ,94(4) :471.
[10 ] Bellocq C ,van Ginneken AC ,Bezzina CR ,et al. Mutation in the KCNQ1 gene leading to the short QT2interval syndrome[J ] . Circulation ,2004 ,109(20) :2394.
[ 11 ] Priori SG,Pandit SV ,Rivolta I ,et al. A novel normof shortQT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene[J ] . Circ Res ,2005 ,96(7) :800.
[12 ] Watanbe T,Yarnaki M,Yamauchi S ,et al. Am J Physiol ,2002 ,282(1) :H212 - H218.
[13 ] 王德国,柯永胜,汪和贵,等. 内洋地黄素拮抗剂减轻心肌缺血再灌注损伤的实验研究[J ] . 中华急诊医学杂志, 2004 ,13(3) :165 - 168.
[14 ] 汪和贵,王德国,柯永胜,等. 地高辛抗血清拮抗内源性洋地黄样物质介导的离体大鼠心脏再灌注心律失常的实验研究[J ] . 中华心律失常学杂志, 2004 ,8(5) :285 - 289.
[15 ] 李翠兰,胡大一. 长QT 综合征的最新研究进展[J ] .心脏杂志,2004 ,16(1) :76 - 79.
[16 ] 刘文玲,胡大一. 遗传性心脏猝死综合征22OO5AHA新观点及新进展[J ] . 中国心脏起搏与心电生理杂志,2006 ,20(1) :16 - 17.
[17 ] 姚艳,浦介麟. 遗传性室性心律失常的药物防治[J ] . 中国心脏起搏与心电生理杂志,2007 ,21 (4) :285 - 287.
[18 ] ACC/ AHA/ ESC 2006 Guidelines for Management of patients with ventricular arrhythmias and the prevention of sudden cardiac death [ J ] . Circulation , 2006 , 114 ( 10) :385.
[19 ] 杨新春,李延辉. 遗传性心律失常综合征[J ] . 临床内科杂志,2006 ,23(7) :443 - 446.
[20 ] Hermida JS ,Denjoy I ,Clerc J ,et al. Hydroquinidine therapy in Brugada syndrome [J ] . Am Coil Cardiol ,2004 ,43(10) :1853.
[21 ] 洪葵. 遗传性室性心律失常[J ] . 临床心电学杂志,2006 ,15(4) :243 - 250.
[ 22 ] Wehrens XH ,Lehnart SE ,Reiken SR ,et al. Protection from cardiac Arrhythmia through ryanodinereceptor2stabilizing protein calstabin2[J ] . Science ,2004 ,304(5668) :292.
[23 ] Lehnart SE ,Wehrens XH ,Laitinen PJ ,et al. Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak[J ] .Circulation ,2004 ,109(25) :3208.
[24 ] Sumitomo N ,Harada K,Nagashima M,et al. Catecholaminergic polymorphic ventricular tachycardia : Electrocardiographic characteristicsand optimal therapeutic strategies to prevent sudden death[J ] . Heart ,2003 ,89(1) :66.
[25 ] 郭成军,张英川,方冬平,等. 导管消融治疗短QT 综合征患者多频率室性心动过速和心室颤动一例[J ] .中华心血管病杂志,2005 ,33(1) :90 - 91.
[26 ] 罗静,杨新春,王乐丰,等. 奎尼丁对吡那地尔诱导的犬右心室跨壁复极离散的影响[J ] . 中华心血管病杂志,2005 ,33(4) :369 - 371.
[27 ] 黄浙勇,葛均波. 干细胞移植治疗心律失常的研究进展[J ] . 中国临床医学,2007 ,14(2) :151 - 154.
[28 ] 马克娟,浦介麟. 遗传性心律失常基因研究近况[J ] . 中国心脏起搏与心电生理杂志,2006 ,20 (1) :4- 7.
来源:中国临床药理学与治疗学 作者:郑建发,柯永胜