Literature DB >> 864488

The peroneal muscular atrophy syndrome. Clinical genetic, electrophysiological and nerve biopsy studies. Part 3. Clinical, electrophysiological and pathological correlations.

W G Bradley, R Madrid, C J Davis.   

Abstract

This report analyses correlations between clinical, electrophysiological and pathological data derived from a series of families with peroneal muscular atrophy. It was found that the observed differences between families in median nerve forearm motor conduction velocity were unlikely to be due to differences in the age or severity of the cases. Similarly it it was unlikely that the pathological differences between cases were due to age or severity of the case. The conduction velocity in the Hypertrophic Neuropathy Group tended to increase slightly with age, while that in other cases tended to fall slightly. The conduction velocity and total myelinated fibre counts were inversely related to the degree of segmental demyelination. The Hypertrophic Neuropathy Group and the Intermediate Group of cases were found to behave differently in a number of correlative analyses, thus supporting the suggestion that they represent different disease entities.

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Mesh:

Year:  1977        PMID: 864488     DOI: 10.1016/0022-510x(77)90043-0

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  11 in total

1.  Genetic linkage studies in hereditary motor and sensory neuropathies.

Authors:  F Leblhuber; F Reisecker; W R Mayr
Journal:  J Neurol       Date:  1986-10       Impact factor: 4.849

Review 2.  Investigation of peripheral neuropathy.

Authors:  J G McLeod
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-03       Impact factor: 10.154

3.  Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathy.

Authors:  Florian P Thomas; Velina Guergueltcheva; Francisco A A Gondim; Ivailo Tournev; Chitharanjan V Rao; Boryana Ishpekova; Laurence J Kinsella; Yi Pan; Thomas J Geller; Ivan Litvinenko; Peter De Jonghe; Steven S Scherer; Albena Jordanova
Journal:  J Neurol       Date:  2016-01-02       Impact factor: 4.849

4.  An autopsy case of peroneal muscular atrophy with rigidity and tremor. Ultrastructural and systematic morphometrical studies on peripheral nerves.

Authors:  Y Itoh; S Yagishita; N Amano; K Iwabuchi
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

5.  Detection of hereditary motor sensory neuropathy type I in childhood.

Authors:  T E Feasby; A F Hahn; C F Bolton; W F Brown; W J Koopman
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-10       Impact factor: 10.154

6.  A combination of spastic paraparesis, polyneuropathy and adrenocortical insufficiency-a childhood form of adrenomyeloneuropathy.

Authors:  K Toifl; B Mamoli; F Waldhauser
Journal:  J Neurol       Date:  1981       Impact factor: 4.849

7.  A family study of Charcot-Marie-Tooth disease.

Authors:  A P Brooks; A E Emery
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318

8.  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

9.  Progressive peroneal muscular atrophy (Charcot-Marie-Tooth disease) associated with beta-thalassemia trait and glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. A clinical and nerve biopsy case.

Authors:  D Inzitari; N Rizzuto; P Antuono; D Sità
Journal:  Ital J Neurol Sci       Date:  1981-08

10.  Charcot-Marie-Tooth disease: study of a large kinship with an intermediate form.

Authors:  A Rossi; C Paradiso; R Cioni; N Rizzuto; G Guazzi
Journal:  J Neurol       Date:  1985       Impact factor: 4.849

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