Literature DB >> 4813428

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

P K Thomas, D B Calne.   

Abstract

Measurements of motor nerve conduction velocity are reported in 88 subjects from 20 families in which a clinical diagnosis of peroneal muscular atrophy had been made in the index cases. The values display a bimodal distribution. The majority of cases show a substantially reduced conduction velocity, a smaller group displaying velocities within the normal range or only slightly decreased. This difference was demonstrated to have a genetic basis.

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Mesh：

Year:  1974        PMID： 4813428      PMCID： PMC494564          DOI： 10.1136/jnnp.37.1.68

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


  19 in total

1.  MOTOR CONDUCTION VELOCITIES IN AMYOTROPHIC LATERAL SCLEROSIS, POLYRADICULONEURITIS AND CHARCOT-MARIE-TOOTH'S DISEASE.

Authors:  S Blom; K E Hagbarth; P O Lundberg
Journal:  Acta Neurol Scand       Date:  1964       Impact factor: 3.209

2.  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

3.  Electrodiagnostic features of Charcot-Marie-Tooth disease.

Authors:  B G CHRISTIE
Journal:  Proc R Soc Med       Date:  1961-04

4.  [Neural muscular atrophy and hypertrophic neuritis; clinical and genealogical data in relation to a family of Bern canton].

Authors:  B LUBAN
Journal:  Schweiz Arch Neurol Psychiatr       Date:  1951

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Authors:  J FRANCOIS; L DESCAMPS
Journal:  Acta Neurol Psychiatr Belg       Date:  1949-09

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Authors:  P K Thomas; R G Lascelles
Journal:  Q J Med       Date:  1967-04

7.  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

8.  Autosomal dominant forms of hereditary hypertrophic neuropathy.

Authors:  P K Thomas; D B Calne; R H King
Journal:  Monogr Hum Genet       Date:  1972

9.  Severe hypomyelination and marked abnormality of conduction in Dejerine-Sottas hypertrophic neuropathy: myelin thickness and compound action potential of sural nerve in vitro.

Authors:  P J Dyck; E H Lambert; K Sanders; P C O'Brien
Journal:  Mayo Clin Proc       Date:  1971-06       Impact factor: 7.616

10.  Pathology of peroneal muscular atrophy (Charcot-Marie-Tooth disease).

Authors:  J T Hughes; B Brownell
Journal:  J Neurol Neurosurg Psychiatry       Date:  1972-10       Impact factor: 10.154
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  27 in total

Review 1.  Intermediate forms of Charcot-Marie-Tooth neuropathy: a review.

Authors:  Garth Nicholson; Simon Myers
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

Review 2.  Investigation of peripheral neuropathy.

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

3.  Motor and sensory conduction velocity in Charcot-Marie-Tooth disease.

Authors:  C Vasilescu; A Florescu
Journal:  J Neurol       Date:  1977-03-21       Impact factor: 4.849

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

Authors:  P Salisachs; L J Findley; M Codina; J M Martinez-Lage
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-02       Impact factor: 10.154

5.  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

6.  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

7.  Peroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindred.

Authors:  J A Frith; J G McLeod; G A Nicholson; F Yang
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-11       Impact factor: 10.154

8.  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

9.  PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease.

Authors:  Hamid Azzedine; Petra Zavadakova; Violaine Planté-Bordeneuve; Maria Vaz Pato; Nuno Pinto; Luca Bartesaghi; Jennifer Zenker; Olivier Poirot; Nathalie Bernard-Marissal; Estelle Arnaud Gouttenoire; Romain Cartoni; Alexandra Title; Giulia Venturini; Jean-Jacques Médard; Edward Makowski; Ludger Schöls; Kristl G Claeys; Claudia Stendel; Andreas Roos; Joachim Weis; Odile Dubourg; José Leal Loureiro; Giovanni Stevanin; Gérard Said; Anthony Amato; Jay Baraban; Eric LeGuern; Jan Senderek; Carlo Rivolta; Roman Chrast
Journal:  Hum Mol Genet       Date:  2013-06-17       Impact factor: 6.150

10.  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
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