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Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): Clinical and neuropathological features of a Japanese family

✍ Scribed by Y Sekijima; S Ohara; S Nakagawa; K Tabata; K Yoshida; H Ishigame; Y Shimizu; N Yanagisawa


Book ID
119469996
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
963 KB
Volume
158
Category
Article
ISSN
0022-510X

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Hereditary motor and sensory neuropathy
✍ Dr. Jessica E. Hoogendijk; Dr. Marianne de Visser; Dr. Pieter A. Bolhuis; Dr. Au πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 539 KB

Forty-four affected individuals, aged 8-68 years (mean 34 years), from six families with hereditary motor and sensory neuropathy type I (HMSN I, Charcot-Marie-Tooth disease type 1) were investigated to determine the clinical and electroneurographical characteristics of the HMSN I subtype that is def