Literature DB >> 6842209

Measurement of motor conduction velocity with Hopf's technique in myotonic dystrophy.

B Rossi, F Sartucci, A Stefanini, G Pucci, F Bianchi.   

Abstract

Hopf's technique was used to measure maximal and minimal motor nerve conduction velocities, and the percentage of fibres with intermediate velocity, in the posterior tibial nerve in patients with myotonic dystrophy. A reduction of maximal and minimal conduction velocities was found. The distribution of fibres with intermediate velocity was nearly identical to that of the control group and the dispersion values were normal. These data do not support the hypothesis that a primary disturbance of the motor neurons is responsible for the muscle changes in myotonic dystrophy. The reduction of the motor nerve conduction velocity, which was an inconstant finding, should not be considered an indication of a neurogenic aetiology of myotonic dystrophy, but only one of the many disorders of a multisystem disease.

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Year:  1983        PMID: 6842209      PMCID: PMC1027273          DOI: 10.1136/jnnp.46.1.93

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


  16 in total

1.  Electrophysiological abnormalities in cases of dystrophia myotonica.

Authors:  S K Mongia; A Lundervold
Journal:  Eur Neurol       Date:  1975       Impact factor: 1.710

2.  Study of the dispersion of motor nerve conduction velocity in charcot-marie-tooth-hoffmann disease and in steinert's syndrome.

Authors:  M R Caccia; S Negri; A Bolardi; A Crippa
Journal:  Z Neurol       Date:  1972

3.  Conduction velocity of motor nerve fibers in progressive spinal atrophy.

Authors:  J Chaco
Journal:  Acta Neurol Scand       Date:  1970       Impact factor: 3.209

4.  Motor nerve conduction velocity in anterior horn lesions.

Authors:  I Hausmanowa-Petrusewicz; J Kopeć
Journal:  Electromyography       Date:  1970 Sep-Oct

5.  The histographic analysis of human muscle biopsies with regard to fiber types. 1. Adult male and female.

Authors:  M H Brooke; W K Engel
Journal:  Neurology       Date:  1969-03       Impact factor: 9.910

6.  Spinal cord limb motor neurons in dystrophia myotonica.

Authors:  J N Walton; D Irving; B E Tomlinson
Journal:  J Neurol Sci       Date:  1977-11       Impact factor: 3.181

7.  New method for the estimation of the number of motor units in a muscle. 2. Duchenne, limb-girdle and facioscapulohumeral, and myotonic muscular dystrophies.

Authors:  J P Ballantyne; S Hansen
Journal:  J Neurol Neurosurg Psychiatry       Date:  1974-11       Impact factor: 10.154

8.  Axonal refractory period of single short toe extensor motor units in neuropathies and neuromuscular diseases.

Authors:  J Borg
Journal:  J Neurol Neurosurg Psychiatry       Date:  1981-12       Impact factor: 10.154

9.  Evidence for neuropathy in myotonic muscular dystrophy.

Authors:  K Kalyanaraman; B H Smith; A L Chadha
Journal:  Bull Los Angeles Neurol Soc       Date:  1973-10

10.  Electrophysiological study of dystrophia myotonica.

Authors:  A J McComas; M J Campbell; R E Sica
Journal:  J Neurol Neurosurg Psychiatry       Date:  1971-04       Impact factor: 10.154

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