Literature DB >> 7069437

Should Charcot-Marie-Tooth disease be genetically subgrouped on motor conduction velocity.

P Salisachs, L J Findley, M Codina, J M Martinez-Lage.   

Abstract

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Year:  1982        PMID： 7069437      PMCID： PMC1083054          DOI： 10.1136/jnnp.45.2.182

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  10 in total

1.  NERVE CONDUCTION AND OTHER STUDIES IN FAMILIES WITH CHARCOT-MARIE-TOOTH DISEASE.

Authors:  N C MYRIANTHOPOULOS; M H LANE; D H SILBERBERG; B L VINCENT
Journal:  Brain       Date:  1964-12       Impact factor: 13.501

2.  Charcot-Marie-Tooth disease associated with "essential tremor": Report of 7 cases and a review of the literature.

Authors:  P Salisachs
Journal:  J Neurol Sci       Date:  1976-05       Impact factor: 3.181

3.  Charcot-Marie-Tooth disease associated with 'essential tremor' and normal and/or slightly diminished motor conduction velocity. Report of 7 cases.

Authors:  P Salisachs; A Codina; S Gimenez-Roldan; J J Zarranz
Journal:  Eur Neurol       Date:  1979       Impact factor: 1.710

4.  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

5.  Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneity.

Authors:  P K Thomas; D B Calne
Journal:  J Neurol Neurosurg Psychiatry       Date:  1974-01       Impact factor: 10.154

6.  [Relations of nerve conduction velocity to histologic findings in peripheral nerves. Based on 49 biopsies of the sural nerve].

Authors:  J Ulrich; E Esslen; F Regli; A Bischoff
Journal:  Dtsch Z Nervenheilkd       Date:  1965-12-14

7.  The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classification.

Authors:  C J Davis; W G Bradley; R Madrid
Journal:  J Genet Hum       Date:  1978-12

8.  Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations.

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

9.  Heredopathia atactica polyneuritiformis (phytanic acid storage disease). A new case with special reference to dietary treatment.

Authors:  V Sahgal; W O Olsen
Journal:  Arch Intern Med       Date:  1975-04

10.  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
  10 in total
  3 in total

1.  Hypertrophic neuropathy in spinocerebellar degeneration. Morphological study of the superficial peroneal nerve in fourteen cases.

Authors:  M Ben Hamida; F Letaief; F Hentati; C Ben Hamida
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

2.  Ataxia and other data reviewed in Charcot-Marie-Tooth and Refsum's disease.

Authors:  P Salisachs
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-12       Impact factor: 10.154

3.  Linkage of autosomal dominant type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1.

Authors:  R J Guiloff; P K Thomas; M Contreras; S Armitage; G Schwarz; E M Sedgwick
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-08       Impact factor: 10.154
  3 in total

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