Resuscitated sudden cardiac death in Andersen-Tawil syndrome.
作者信息
Airey Kelly J, Etheridge Susan P, Tawil Rabi, Tristani-Firouzi Martin
机构信息
Division of Cardiology, University of Utah, Salt Lake City, Utah, USA.
出版信息
Heart Rhythm. 2009 Dec;6(12):1814-7. doi: 10.1016/j.hrthm.2009.08.032. Epub 2009 Aug 29.
Abstract
摘要
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本文引用的文献
1
Sudden cardiac death in Andersen-Tawil syndrome.安德森-陶威尔综合征中的心脏性猝死
Europace. 2007 Mar;9(3):162-6. doi: 10.1093/europace/eul188. Epub 2007 Feb 1.
2
Andersen-Tawil syndrome.安德森-陶威尔综合征
Indian Pacing Electrophysiol J. 2006 Jan 1;6(1):32-43.
3
Modeling of IK1 mutations in human left ventricular myocytes and tissue.人类左心室心肌细胞和组织中IK1突变的建模
Am J Physiol Heart Circ Physiol. 2007 Jan;292(1):H549-59. doi: 10.1152/ajpheart.00701.2006. Epub 2006 Aug 25.
4
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.携带KCNJ2基因突变的安德森-陶威尔综合征患者的心电图特征：特征性T-U波形态可预测KCNJ2基因型。
Circulation. 2005 May 31;111(21):2720-6. doi: 10.1161/CIRCULATIONAHA.104.472498. Epub 2005 May 23.
5
Polymorphic ventricular tachycardia and KCNJ2 mutations.多形性室性心动过速与KCNJ2基因突变
Heart Rhythm. 2004 Jul;1(2):235-41. doi: 10.1016/j.hrthm.2004.02.017.
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PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome.内向整流钾通道2.1（Kir2.1）的磷脂酰肌醇-4,5-二磷酸（PIP2）结合残基是导致安德森综合征的突变的常见靶点。
Neurology. 2003 Jun 10;60(11):1811-6. doi: 10.1212/01.wnl.0000072261.14060.47.
7
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome.Kir2.1基因的突变导致安德森综合征的发育性和发作性电表型。
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Cardiac pacing in the long QT syndrome: review of available data and practical recommendations.
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9
Propofol in anesthesia. Mechanism of action, structure-activity relationships, and drug delivery.丙泊酚在麻醉中的应用。作用机制、构效关系及药物递送
Curr Med Chem. 2000 Feb;7(2):249-71. doi: 10.2174/0929867003375335.
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Andersen's syndrome: a distinct periodic paralysis.
Ann Neurol. 1997 Sep;42(3):305-12. doi: 10.1002/ana.410420306.
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