Movement Disorders (revue)

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Electrophysiology of the corticomotoneurone pathways in patients with movement disorders

Identifieur interne : 003695 ( Istex/Corpus ); précédent : 003694; suivant : 003696

Electrophysiology of the corticomotoneurone pathways in patients with movement disorders

Auteurs : P. D. Thompson ; J. P. R. Dick ; B. L. Day ; J. C. Rothwell ; A. Berardelli ; T. Kachi ; C. D. Marsden

Source :

RBID : ISTEX:F0ACE88E36EAD95399D3F98FE03C5F9891B7B1EC

English descriptors

Abstract

The corticomotoneurone pathways were examined in 21 patients with movement disorders, using the technique of percutaneous electrical stimulation of the motor cortex. Conduction in these pathways was assessed by measuring the latency to onset of electromyographic activity in the muscles of the upper limb after cortical stimulation. In all patients [five with primary (idiopathic) torsion dystonia and two with secondary (symptomatic) hemidystonia, seven with Huntington's disease, four with essential tremor, and three with Parkinson's disease] central motor conduction was normal. This and other evidence suggests that the origin of the disorder of movement in these conditions lies in the delivery of abnormal motor commands to a normal corticomotoneuronal system.

Url:
DOI: 10.1002/mds.870010205

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ISTEX:F0ACE88E36EAD95399D3F98FE03C5F9891B7B1EC

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<p>The corticomotoneurone pathways were examined in 21 patients with movement disorders, using the technique of percutaneous electrical stimulation of the motor cortex. Conduction in these pathways was assessed by measuring the latency to onset of electromyographic activity in the muscles of the upper limb after cortical stimulation. In all patients [five with primary (idiopathic) torsion dystonia and two with secondary (symptomatic) hemidystonia, seven with Huntington's disease, four with essential tremor, and three with Parkinson's disease] central motor conduction was normal. This and other evidence suggests that the origin of the disorder of movement in these conditions lies in the delivery of abnormal motor commands to a normal corticomotoneuronal system.</p>
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<title>Electrophysiology of the corticomotoneurone pathways in patients with movement disorders</title>
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<description>Correspondence: University Department of Neurology, London SE5 8AF, England</description>
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<abstract lang="en">The corticomotoneurone pathways were examined in 21 patients with movement disorders, using the technique of percutaneous electrical stimulation of the motor cortex. Conduction in these pathways was assessed by measuring the latency to onset of electromyographic activity in the muscles of the upper limb after cortical stimulation. In all patients [five with primary (idiopathic) torsion dystonia and two with secondary (symptomatic) hemidystonia, seven with Huntington's disease, four with essential tremor, and three with Parkinson's disease] central motor conduction was normal. This and other evidence suggests that the origin of the disorder of movement in these conditions lies in the delivery of abnormal motor commands to a normal corticomotoneuronal system.</abstract>
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<topic>Corticomotoneurone pathways</topic>
<topic>Movement disorders</topic>
<topic>Central motor conduction</topic>
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<title>Movement Disorders</title>
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<identifier type="ISSN">0885-3185</identifier>
<identifier type="eISSN">1531-8257</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-8257</identifier>
<identifier type="PublisherID">MDS</identifier>
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<date>1986</date>
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