Hereditary motor and sensory neuropathies or Charcot–Marie–Tooth diseases: An update-Reference-Cited by-同舟云学术

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Hereditary motor and sensory neuropathies or Charcot–Marie–Tooth diseases: An update

Published:2014-12 Issue:1-2 Volume:347 Page:14-22
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Tazir Meriem,Hamadouche Tarik,Nouioua Sonia,Mathis Stephane,Vallat Jean-Michel

Funder

Algiers University

Ministry of Health and Population (Algeria)

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference55 articles.

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

2. Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneity;Thomas;J Neurol Neurosurg Psychiatry,1974

3. The clinical features of hereditary motor and sensory neuropathy types I and II;Harding;Brain,1980

4. Autosomal recessive forms of hereditary motor and sensory neuropathy;Harding;J Neurol Neurosurg Psychiatry,1980

5. Connexin mutations in X-linked Charcot–Marie–Tooth disease;Bergoffen;Science,1993

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