Abnormal conduction in corticospinal pathways in Wilson's disease: Investigation of nine cases with magnetic brain stimulation
Identifieur interne : 006202 ( Main/Curation ); précédent : 006201; suivant : 006203Abnormal conduction in corticospinal pathways in Wilson's disease: Investigation of nine cases with magnetic brain stimulation
Auteurs : Meyer [Allemagne] ; T. C. Britton [Allemagne] ; C. Bischoff [Allemagne] ; J. Machetanz [Allemagne] ; R. Benecke [Allemagne] ; B. Conrad [Allemagne]Source :
- Movement Disorders [ 0885-3185 ] ; 1991.
English descriptors
- KwdEn :
- Adult, Electromagnetic Fields, Electromyography, Follow-Up Studies, Hepatolenticular Degeneration (diagnosis), Hepatolenticular Degeneration (drug therapy), Hepatolenticular Degeneration (physiopathology), Humans, Motor Cortex (drug effects), Motor Cortex (physiopathology), Muscle Contraction (drug effects), Muscle Contraction (physiology), Muscles (innervation), Neurologic Examination, Penicillamine (therapeutic use), Pyramidal Tracts (drug effects), Pyramidal Tracts (physiopathology), Synaptic Transmission (drug effects), Synaptic Transmission (physiology), Wilson's disease, motor responses.
- MESH :
- chemical , therapeutic use : Penicillamine.
- diagnosis : Hepatolenticular Degeneration.
- drug effects : Motor Cortex, Muscle Contraction, Pyramidal Tracts, Synaptic Transmission.
- drug therapy : Hepatolenticular Degeneration.
- innervation : Muscles.
- physiology : Muscle Contraction, Synaptic Transmission.
- physiopathology : Hepatolenticular Degeneration, Motor Cortex, Pyramidal Tracts.
- Adult, Electromagnetic Fields, Electromyography, Follow-Up Studies, Humans, Neurologic Examination.
Abstract
Electromyographic (EMG) responses evoked by transcranial magnetic brain stimulation were studied in nine patients with Wilson's disease (WD). Six of the nine patients had prolonged central motor latencies (CMLs), reduced amplitude, or absent responses in at least one of the examined muscles. In one patient, abnormal EMG responses normalized following treatment with penicillamine. Pathophysiologically abnormal EMG responses might result from a potentially reversible impairment of corticomotoneuronal pathways and/or a reduced excitability of motoneurons due to basal ganglia dysfunction. The possible pathophysiological mechanisms are discussed.
Url:
DOI: 10.1002/mds.870060409
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: Pour aller vers cette notice dans l'étape Curation :003515
- to stream Istex, to step Curation: Pour aller vers cette notice dans l'étape Curation :003515
- to stream Istex, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :004345
- to stream PubMed, to step Corpus: Pour aller vers cette notice dans l'étape Curation :004E56
- to stream PubMed, to step Curation: Pour aller vers cette notice dans l'étape Curation :004E56
- to stream PubMed, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :004E54
- to stream Ncbi, to step Merge: Pour aller vers cette notice dans l'étape Curation :001638
- to stream Ncbi, to step Curation: Pour aller vers cette notice dans l'étape Curation :001638
- to stream Ncbi, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :001638
- to stream Main, to step Merge: Pour aller vers cette notice dans l'étape Curation :009506
Links to Exploration step
ISTEX:887C1BD18DCBEEFF2A52BEDA62EEA409C8B0F6A7Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Abnormal conduction in corticospinal pathways in Wilson's disease: Investigation of nine cases with magnetic brain stimulation</title>
<author><name sortKey="Meyer" sort="Meyer" uniqKey="Meyer" last="Meyer">Meyer</name>
</author>
<author><name sortKey="Britton, T C" sort="Britton, T C" uniqKey="Britton T" first="T. C." last="Britton">T. C. Britton</name>
</author>
<author><name sortKey="Bischoff, C" sort="Bischoff, C" uniqKey="Bischoff C" first="C." last="Bischoff">C. Bischoff</name>
</author>
<author><name sortKey="Machetanz, J" sort="Machetanz, J" uniqKey="Machetanz J" first="J." last="Machetanz">J. Machetanz</name>
</author>
<author><name sortKey="Benecke, R" sort="Benecke, R" uniqKey="Benecke R" first="R." last="Benecke">R. Benecke</name>
</author>
<author><name sortKey="Conrad, B" sort="Conrad, B" uniqKey="Conrad B" first="B." last="Conrad">B. Conrad</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:887C1BD18DCBEEFF2A52BEDA62EEA409C8B0F6A7</idno>
<date when="1991" year="1991">1991</date>
<idno type="doi">10.1002/mds.870060409</idno>
<idno type="url">https://api.istex.fr/document/887C1BD18DCBEEFF2A52BEDA62EEA409C8B0F6A7/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">003515</idno>
<idno type="wicri:Area/Istex/Curation">003515</idno>
<idno type="wicri:Area/Istex/Checkpoint">004345</idno>
<idno type="wicri:doubleKey">0885-3185:1991:Meyer:abnormal:conduction:in</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:1661845</idno>
<idno type="wicri:Area/PubMed/Corpus">004E56</idno>
<idno type="wicri:Area/PubMed/Curation">004E56</idno>
<idno type="wicri:Area/PubMed/Checkpoint">004E54</idno>
<idno type="wicri:Area/Ncbi/Merge">001638</idno>
<idno type="wicri:Area/Ncbi/Curation">001638</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">001638</idno>
<idno type="wicri:doubleKey">0885-3185:1991:Meyer B:abnormal:conduction:in</idno>
<idno type="wicri:Area/Main/Merge">009506</idno>
<idno type="wicri:Area/Main/Curation">006202</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Abnormal conduction in corticospinal pathways in Wilson's disease: Investigation of nine cases with magnetic brain stimulation</title>
<author><name sortKey="Meyer" sort="Meyer" uniqKey="Meyer" last="Meyer">Meyer</name>
<affiliation wicri:level="3"><country>Allemagne</country>
<placeName><settlement type="city">Munich</settlement>
<region type="land" nuts="1">Bavière</region>
<region type="district" nuts="2">District de Haute-Bavière</region>
</placeName>
<wicri:orgArea>Department of Neurology of the Technical University in Munich</wicri:orgArea>
</affiliation>
</author>
<author><name sortKey="Britton, T C" sort="Britton, T C" uniqKey="Britton T" first="T. C." last="Britton">T. C. Britton</name>
<affiliation wicri:level="1"><country xml:lang="fr" wicri:curation="lc">Allemagne</country>
<wicri:regionArea>Department of Neurology, Heinrich Heine University in Düsseldorf, Düsseldorf</wicri:regionArea>
<wicri:noRegion>Düsseldorf</wicri:noRegion>
<wicri:noRegion>Düsseldorf</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Bischoff, C" sort="Bischoff, C" uniqKey="Bischoff C" first="C." last="Bischoff">C. Bischoff</name>
<affiliation wicri:level="3"><country>Allemagne</country>
<placeName><settlement type="city">Munich</settlement>
<region type="land" nuts="1">Bavière</region>
<region type="district" nuts="2">District de Haute-Bavière</region>
</placeName>
<wicri:orgArea>Department of Neurology of the Technical University in Munich</wicri:orgArea>
</affiliation>
</author>
<author><name sortKey="Machetanz, J" sort="Machetanz, J" uniqKey="Machetanz J" first="J." last="Machetanz">J. Machetanz</name>
<affiliation wicri:level="3"><country>Allemagne</country>
<placeName><settlement type="city">Munich</settlement>
<region type="land" nuts="1">Bavière</region>
<region type="district" nuts="2">District de Haute-Bavière</region>
</placeName>
<wicri:orgArea>Department of Neurology of the Technical University in Munich</wicri:orgArea>
</affiliation>
</author>
<author><name sortKey="Benecke, R" sort="Benecke, R" uniqKey="Benecke R" first="R." last="Benecke">R. Benecke</name>
<affiliation wicri:level="1"><country xml:lang="fr" wicri:curation="lc">Allemagne</country>
<wicri:regionArea>Department of Neurology, Heinrich Heine University in Düsseldorf, Düsseldorf</wicri:regionArea>
<wicri:noRegion>Düsseldorf</wicri:noRegion>
<wicri:noRegion>Düsseldorf</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Conrad, B" sort="Conrad, B" uniqKey="Conrad B" first="B." last="Conrad">B. Conrad</name>
<affiliation wicri:level="3"><country>Allemagne</country>
<placeName><settlement type="city">Munich</settlement>
<region type="land" nuts="1">Bavière</region>
<region type="district" nuts="2">District de Haute-Bavière</region>
</placeName>
<wicri:orgArea>Department of Neurology of the Technical University in Munich</wicri:orgArea>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="1991">1991</date>
<biblScope unit="vol">6</biblScope>
<biblScope unit="issue">4</biblScope>
<biblScope unit="page" from="320">320</biblScope>
<biblScope unit="page" to="323">323</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">887C1BD18DCBEEFF2A52BEDA62EEA409C8B0F6A7</idno>
<idno type="DOI">10.1002/mds.870060409</idno>
<idno type="ArticleID">MDS870060409</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Electromagnetic Fields</term>
<term>Electromyography</term>
<term>Follow-Up Studies</term>
<term>Hepatolenticular Degeneration (diagnosis)</term>
<term>Hepatolenticular Degeneration (drug therapy)</term>
<term>Hepatolenticular Degeneration (physiopathology)</term>
<term>Humans</term>
<term>Motor Cortex (drug effects)</term>
<term>Motor Cortex (physiopathology)</term>
<term>Muscle Contraction (drug effects)</term>
<term>Muscle Contraction (physiology)</term>
<term>Muscles (innervation)</term>
<term>Neurologic Examination</term>
<term>Penicillamine (therapeutic use)</term>
<term>Pyramidal Tracts (drug effects)</term>
<term>Pyramidal Tracts (physiopathology)</term>
<term>Synaptic Transmission (drug effects)</term>
<term>Synaptic Transmission (physiology)</term>
<term>Wilson's disease</term>
<term>motor responses</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Penicillamine</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Hepatolenticular Degeneration</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Motor Cortex</term>
<term>Muscle Contraction</term>
<term>Pyramidal Tracts</term>
<term>Synaptic Transmission</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Hepatolenticular Degeneration</term>
</keywords>
<keywords scheme="MESH" qualifier="innervation" xml:lang="en"><term>Muscles</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Muscle Contraction</term>
<term>Synaptic Transmission</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Hepatolenticular Degeneration</term>
<term>Motor Cortex</term>
<term>Pyramidal Tracts</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Electromagnetic Fields</term>
<term>Electromyography</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Neurologic Examination</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Electromyographic (EMG) responses evoked by transcranial magnetic brain stimulation were studied in nine patients with Wilson's disease (WD). Six of the nine patients had prolonged central motor latencies (CMLs), reduced amplitude, or absent responses in at least one of the examined muscles. In one patient, abnormal EMG responses normalized following treatment with penicillamine. Pathophysiologically abnormal EMG responses might result from a potentially reversible impairment of corticomotoneuronal pathways and/or a reduced excitability of motoneurons due to basal ganglia dysfunction. The possible pathophysiological mechanisms are discussed.</div>
</front>
</TEI>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Curation
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 006202 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Curation/biblio.hfd -nk 006202 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= Main |étape= Curation |type= RBID |clé= ISTEX:887C1BD18DCBEEFF2A52BEDA62EEA409C8B0F6A7 |texte= Abnormal conduction in corticospinal pathways in Wilson's disease: Investigation of nine cases with magnetic brain stimulation }}
This area was generated with Dilib version V0.6.23. |