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先天性QT延长综合征合并阵发性三度房室传导阻滞一例 被引量:3

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出处 《中华心血管病杂志》 CAS CSCD 北大核心 2005年第8期768-769,共2页 Chinese Journal of Cardiology
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  • 1Schwartz PJ, Moss AJ, Vincent GM,et al. Diagnostic criteria for the long QT syndrome: an update. Circulation, 1993, 88:782-784. 被引量:1
  • 2Trippel DL, Parsons MK, Gillette PC. Infants with long-QT syndrome and 2: 1 atrioventricular block. Am Heart J, 1995, 130: 1130-1134. 被引量:1
  • 3Moss AJ, Zareba W, Benhorin J, et al. ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome. Circulation, 1995, 92:2929-2934. 被引量:1
  • 4Pruvot E, De Torrente A, De Ferrari GM, et al. Two-to-one AV block associated with the congenital long QT syndrome. J Cardiovasc Electrophysiol, 1999, 10: 108-113. 被引量:1
  • 5Piipo K, Laitinen P, Swan H,et al. Homozygosity for HERG potassium channel mutation causes a severe from of long QT syndrome: identification of an apparent founder mutation in Finns. J Am Coll Cardiol, 2000, 35: 1264-1267. 被引量:1
  • 6Lupoglazoff JM, Cheav T, Baroudi G, et al. Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block. Circ Res, 2001, 89:16. 被引量:1
  • 7Tan HL, Bink-Boelkens MT, Bezzina C, et al. A sodium-channel mutation causes isolated cardiac conduction disease. Nature, 2001, 409: 1043-1047. 被引量:1

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