Detection of hereditary motor sensory neuropathy type I in childhood.

Author:

Feasby T E,Hahn A F,Bolton C F,Brown W F,Koopman W J

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference15 articles.

1. Classification and electrodiagnosis of hereditary neuropathies;Thomas, P.K.,1987

2. The clinical features of Hereditary Motor and Sensory NeuropathyTypes I and II;Harding, A.E.; Thomas, P.K.;Brain,1980

3. The hypertrophic forms of motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN III) in childhood;Ouvrier, R.A.; McLeod, J.G.; Conchin, T.E.;Brain,1987

4. Lower motor and primnary sensory neuron disease with peroneal muscular atrophy. I. Neurologic, genetic and electrophysiological findings in hereditary polyneuropathy;Dyck, P.J.; Lambert, E.H.;Arch Neurol,1968

5. Lower motor and primary sensory neuron disease with peroneal muscular atrophy. II. Neurologic, genetic and electrophysiological findings in various neuronal degenerations;Dyck, P.J.; Lambert, E.H.;Arch Neurol,1968

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