Myoclonus in spinal dysraphism
Identifieur interne : 001C24 ( Istex/Corpus ); précédent : 001C23; suivant : 001C25Myoclonus in spinal dysraphism
Auteurs : Jane E. Warren ; Marie Vidailhet ; Christopher S. Kneebone ; Niall P. Quinn ; Philip D. ThompsonSource :
- Movement Disorders [ 0885-3185 ] ; 2003-08.
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- KwdEn :
Abstract
Two cases of segmental myoclonus occurring in association with spinal dysraphism are described. In one, myoclonus of paralysed legs arose below a region of spinal cord lacking any normal function, illustrating the capacity of the isolated spinal cord to generate and maintain rhythmic activity independent of supraspinal influences. © 2003 Movement Disorder Society
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DOI: 10.1002/mds.10469
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</titleInfo>
<subject><genre>article category</genre>
<topic>Clinical/Scientific Note</topic>
</subject>
<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>
<part><date>2003</date>
<detail type="volume"><caption>vol.</caption>
<number>18</number>
</detail>
<detail type="issue"><caption>no.</caption>
<number>8</number>
</detail>
<extent unit="pages"><start>961</start>
<end>964</end>
<total>3</total>
</extent>
</part>
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<identifier type="istex">D784175ABBBA0638A1564CD13CAB974ACB54C378</identifier>
<identifier type="DOI">10.1002/mds.10469</identifier>
<identifier type="ArticleID">MDS10469</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2003 Movement Disorder Society</accessCondition>
<recordInfo><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin>
<recordContentSource>WILEY</recordContentSource>
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