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Comparison of Electrophysiological Findings between CIDP and HMSN-1 Osamu Hasegawa 1 , Shunsuke Matsumoto 1,2,3 , Mitsuharu Iino 1,4 , Ryuko Kurita 1 , Yukiko Kubota 5 1Department of Neurology, Yokohama City University School of Medicine 5Division of Clinical Laboratory, Yokohama City University School of Medicine Keyword: hereditary motor sensory neuropathy(HMSN) , Charcot-Marie-Tooth neuropathy , chronic inflammatory demyelinating polyneuropathy(CIDP) , electrophysiological findings , conduction block pp.411-414
Published Date 1999/5/1
DOI https://doi.org/10.11477/mf.1406901435
  • Abstract
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Chronic inflammatory demyelinating polyneuropathy (CIDP) and hereditary motor sensory neuropathy type 1 (HMSN-1) are representative myelinopathies. In order to differentiate changes in acquired and con-genital demyelinating neuropathies, we studied elec-trophysiologically 9 patients with active phase of CIDP (36.0±17.6 years old; mean±SD) and 7 patients with genetically-proven HMSN-1 A (56.0±13.6 years old). Motor conduction studies demonstrated longitudinal uniformity in HMSN-1, contrariwise focal conduction block or conduction delay in CIDP.


Copyright © 1999, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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