Literature DB >> 3500148

Hereditary motor and sensory neuropathies: a genetic and epidemiological study in the province of Turin, Italy.

A Chiò1, A Tribolo, F Brignolio, M Leone, P Meineri, M G Rosso, M Mostert, D Schiffer.   

Abstract

A clinical, genetic and epidemiological study of hereditary motor and sensory neuropathies (HMSN) was performed in the province of Turin, Italy. The patients were allocated to 5 groups, according to genetic and electroneurographic features. The high proportion of males among recessive and sporadic cases in the present series may suggest the existence of a recessive X-linked form of the disease. The crude prevalence rate was 3.18 (+/- 0.72)/100.000 population for all cases. The slow progression rate and the frequently mild symptoms of the disease, already suggested in literature, are confirmed by the analysis of the survival curves of the cases.

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Year:  1987        PMID: 3500148     DOI: 10.1007/BF02335741

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN: 0392-0461


  22 in total

1.  Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography.

Authors:  F Buchthal; F Behse
Journal:  Brain       Date:  1977-03       Impact factor: 13.501

2.  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

3.  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

4.  Wide spectrum of motor conduction velocity in Charcot-Marie-Tooth disease. An anatomico-physiological interpretation.

Authors:  P Salisachs
Journal:  J Neurol Sci       Date:  1974-09       Impact factor: 3.181

5.  Patterns of neurologic diseases on guam.

Authors:  K M Chen; J A Brody; L T Kurland
Journal:  Arch Neurol       Date:  1968-12

6.  Genetic aspects of hereditary motor and sensory neuropathy (types I and II).

Authors:  A E Harding; P K Thomas
Journal:  J Med Genet       Date:  1980-10       Impact factor: 6.318

7.  The nosology of genetic peripheral neuropathies in Swedish children.

Authors:  B Hagberg; B Westerberg
Journal:  Dev Med Child Neurol       Date:  1983-02       Impact factor: 5.449

8.  Hereditary motor-sensory neuropathy (HMSN): possible X-linked dominant inheritance.

Authors:  L H Phillips; T E Kelly; P Schnatterly; D Parker
Journal:  Neurology       Date:  1985-04       Impact factor: 9.910

9.  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

10.  Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. analysis and examples.

Authors:  R Peto; M C Pike; P Armitage; N E Breslow; D R Cox; S V Howard; N Mantel; K McPherson; J Peto; P G Smith
Journal:  Br J Cancer       Date:  1977-01       Impact factor: 7.640

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  1 in total

1.  Myasthenia gravis associated with Charcot-Marie-Tooth neuropathy: report of a case.

Authors:  G Salemi; B Fierro; G Savettieri; M Maggio; I Lupo; S Ferrari; F Piccoli
Journal:  Ital J Neurol Sci       Date:  1992-06
  1 in total

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