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运动神经元病中的多模态诱发电位

Multimodality evoked potentials in motor neuron disease.

作者信息

Subramaniam J S, Yiannikas C

机构信息

Department of Clinical Neurophysiology, Westmead Hospital, New South Wales, Australia.

出版信息

Arch Neurol. 1990 Sep;47(9):989-94. doi: 10.1001/archneur.1990.00530090063014.

Abstract

We performed median and tibial nerve somatosensory evoked potentials (SEPs), pattern-shift visual evoked potentials (PSVEPs), and brain-stem auditory evoked potentials (BAEPs) on 27 patients with motor neuron disease (MND). Median and tibial nerve SEPs were abnormal in 8 (30%) of 27 and 3 (14%) of 21 patients tested, respectively. Central and peripheral abnormalities were recorded in the absence of spondylosis. As a group, patients with MND and no evidence of cervical spondylosis had normal conduction to Erb's point following median nerve stimulation, but conduction times beyond this point were prolonged. The PSVEPs and BAEPs were within normal limits in all patients, excluding abnormalities attributable to other disease, but the group P100 latency was significantly prolonged in the group with MND. The BAEPs were normal in the group with MND. This study provides neurophysiological evidence of sensory system involvement in MND.

摘要

我们对27例运动神经元病(MND)患者进行了正中神经和胫神经体感诱发电位(SEP)、图形翻转视觉诱发电位(PSVEP)以及脑干听觉诱发电位(BAEP)检查。在接受检查的27例患者中,8例(30%)正中神经SEP异常,21例患者中3例(14%)胫神经SEP异常。在无颈椎病的情况下记录到中枢和周围神经异常。总体而言,无颈椎病证据的MND患者在正中神经刺激后至Erb点的传导正常,但超过该点的传导时间延长。除其他疾病所致异常外,所有患者的PSVEP和BAEP均在正常范围内,但MND组的P100潜伏期显著延长。MND组的BAEP正常。本研究提供了感觉系统受累于MND的神经生理学证据。

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