Literature DB >> 3163721

Hereditary motor and sensory neuropathy type II with axonal lesions.

J Julien, C Vital, A Lagueny, X Ferrer.   

Abstract

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Year:  1988        PMID： 3163721     DOI： 10.1007/bf00314360

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  3 in total

1.  Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.

Authors:  P J Dyck; E H Lambert
Journal:  Arch Neurol       Date:  1968-06

2.  [Anatomo-clinical study of a neuronal form of Charcot-Marie-Tooth disease].

Authors:  M Dupuis; J M Brucher; R Gonsette
Journal:  Rev Neurol (Paris)       Date:  1983       Impact factor: 2.607

3.  The clinical features of hereditary motor and sensory neuropathy types I and II.

Authors:  A E Harding; P K Thomas
Journal:  Brain       Date:  1980-06       Impact factor: 13.501
  3 in total
  1 in total

1.  Degeneration of anterior horn cell in neuronal type of Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type II): a Golgi study.

Authors:  S Ono; K Hara; H Sasaki; I Sugano; K Nagao
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088
  1 in total

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