Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with Charcot–Marie–Tooth disease 1A duplication-Reference-Cited by-同舟云学术

Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with Charcot–Marie–Tooth disease 1A duplication

Published:2000-08 Issue:6 Volume:10 Page:419-424
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Berciano José,Garcı́a Antonio,Calleja Jesús,Combarros Onofre

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference30 articles.

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2. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy;Dyck;I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies. Arch Neurol,1968

3. From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins;Harding;Brain,1995

4. Evolution of nerve conduction abnormalities in children with dominant hypertrophic neuropathy of the Charcot–Marie–Tooth type;Gutmann;Muscle Nerve,1983

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