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作 者:Terwindt G.M. Kors E.E. Vein A.A. 姚庆和
出 处:《世界核心医学期刊文摘(神经病学分册)》2005年第4期46-46,共1页Digest of the World Core Medical Journals:Clinical Neurology
摘 要:Twelve familial hemiplegic migraine (FHM) patients (6 with the I1811L mutation in CACNA1A, 3 with M731T mutation in ATP1A2, and 3 without known mutations) and 10 control subjects underwent single- fiber EMG. Mean jitter did not differ significantly between patients and control subjects or among patients. No blocking was found. The results suggest that neuromuscular function is normal in FHM.Twelve familial hemiplegic migraine (FHM) patients (6 with the I1811L mutation in CACNA1A, 3 with M731T mutation in ATP1A2, and 3 without known mutations) and 10 control subjects underwent single- fiber EMG. Mean jitter did not differ significantly between patients and control subjects or among patients. No blocking was found. The results suggest that neuromuscular function is normal in FHM.
分 类 号:R747.2[医药卫生—神经病学与精神病学]
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