Usefulness of Valsalva manoeuvre and cold pressor test for evaluation of arrhythmias in long QT syndrome.
作者信息
Rubin S A, Brundage B, Mayer W, Chatterjee K
出版信息
Br Heart J. 1979 Oct;42(4):490-2. doi: 10.1136/hrt.42.4.490.
Abstract
摘要
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Usefulness of Valsalva manoeuvre and cold pressor test for evaluation of arrhythmias in long QT syndrome.瓦尔萨尔瓦动作和冷加压试验在评估长QT综合征心律失常中的应用价值。
Br Heart J. 1979 Oct;42(4):490-2. doi: 10.1136/hrt.42.4.490.
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本文引用的文献
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Antifibrillatory drugs.抗纤颤药物。
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2
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A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN.一种新的儿童家族性心脏综合征。
J Ir Med Assoc. 1964 Apr;54:103-6.
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Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death.先天性聋哑、伴有Q-T间期延长的功能性心脏病及猝死。
Am Heart J. 1957 Jul;54(1):59-68. doi: 10.1016/0002-8703(57)90079-0.
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[The surdo-cardiac syndrome].[聋哑-心脏综合征]
Nord Med. 1967 Nov 2;78(44):1443-50.
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Electrophysiological effects of diphenylhydantoin on canine purkinje fibers.苯妥英钠对犬浦肯野纤维的电生理效应。
Circ Res. 1968 Feb;22(2):221-36. doi: 10.1161/01.res.22.2.221.
7
Heritable Q-T prolongation without deafness.遗传性Q-T间期延长但无耳聋。
Circulation. 1970 Jan;41(1):39-48. doi: 10.1161/01.cir.41.1.39.
8
Q-T prolongation and ventricular arrhythmias, with and without deafness, in the same family.同一家族中伴有或不伴有耳聋的Q-T间期延长和室性心律失常。
Am J Cardiol. 1972 May;29(5):702-11. doi: 10.1016/0002-9149(72)90174-9.
9
Hereditary prolongation of the Q-T interval. Genetic observations and management in three families with twelve affected members.遗传性Q-T间期延长。对三个家族中12名患者的遗传学观察及处理
Am J Cardiol. 1976 Feb;37(2):237-43. doi: 10.1016/0002-9149(76)90318-0.
10
The long Q-T syndrome.长QT综合征。
Am Heart J. 1975 Mar;89(3):378-90. doi: 10.1016/0002-8703(75)90089-7.
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