Clinical-sonographic and neurophysiological comparisons in hereditary motor and sensory neuropathy

The article presents the results of ultrasound studies inpatients with hereditary motor and sensory neuropathy, orCharcot-Marie-Tooth disease (CMT). Based on standardelectroneuromiography, the patients were divided into two groupswith demyelinating (n=25) or axonal (n=31) process, CMT1 andCMT2 respe...

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Bibliographic Details
Main Authors: N. B. Vuytsik, A. O. Chechetkin, E. V. Pavlov, S. A. Klushnikov, S. N. Illarioshkin
Format: Article
Language:English
Published: Research Center of Neurology 2017-02-01
Series:Анналы клинической и экспериментальной неврологии
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Online Access:https://annaly-nevrologii.com/journal/pathID/article/viewFile/169/11