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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Research Center of Neurology
2017-02-01
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Series: | Анналы клинической и экспериментальной неврологии |
Subjects: | |
Online Access: | https://annaly-nevrologii.com/journal/pathID/article/viewFile/169/11 |