Interictal myoclonus with paroxysmal kinesigenic dyskinesia
Identifieur interne : 003B12 ( Istex/Corpus ); précédent : 003B11; suivant : 003B13Interictal myoclonus with paroxysmal kinesigenic dyskinesia
Auteurs : Valerie Cochen De Cock ; Frederic Bourdain ; Emmanuelle Apartis ; Jean Marc Trocello ; Emmanuel Roze ; Marie VidailhetSource :
- Movement Disorders [ 0885-3185 ] ; 2006-09.
English descriptors
Abstract
We report a new association between interictal myoclonus and paroxysmal kinesigenic dyskinesia (PKD) in 2 patients. By definition, PKD is transient, but the overexcitability of the neuronal system that induces these attacks may be permanent. Interictal myoclonus could be a manifestation of permanent overexcitability. © 2006 Movement Disorder Society
Url:
DOI: 10.1002/mds.20992
Links to Exploration step
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</role>
</name>
<name type="personal"><namePart type="given">Emmanuelle</namePart>
<namePart type="family">Apartis</namePart>
<namePart type="termsOfAddress">MD, PhD</namePart>
<affiliation>Service de neurologie, Hôpital Saint Antoine, Assistance Publique Hôpitaux de Paris, France</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Jean Marc</namePart>
<namePart type="family">Trocello</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Service de neurologie, Hôpital Saint Antoine, Assistance Publique Hôpitaux de Paris, France</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Emmanuel</namePart>
<namePart type="family">Roze</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Service de neurologie, Hôpital Saint Antoine, Assistance Publique Hôpitaux de Paris, France</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Marie</namePart>
<namePart type="family">Vidailhet</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Service de neurologie, Hôpital Saint Antoine, Assistance Publique Hôpitaux de Paris, France</affiliation>
<role><roleTerm type="text">author</roleTerm>
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<typeOfResource>text</typeOfResource>
<genre authority="originalCategForm">article</genre>
<originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<place><placeTerm type="text">Hoboken</placeTerm>
</place>
<dateIssued encoding="w3cdtf">2006-09</dateIssued>
<dateCaptured encoding="w3cdtf">2005-11-11</dateCaptured>
<dateValid encoding="w3cdtf">2006-02-20</dateValid>
<copyrightDate encoding="w3cdtf">2006</copyrightDate>
</originInfo>
<language><languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
</language>
<physicalDescription><internetMediaType>text/html</internetMediaType>
<extent unit="figures">1</extent>
<extent unit="references">11</extent>
<extent unit="words">1373</extent>
</physicalDescription>
<abstract lang="en">We report a new association between interictal myoclonus and paroxysmal kinesigenic dyskinesia (PKD) in 2 patients. By definition, PKD is transient, but the overexcitability of the neuronal system that induces these attacks may be permanent. Interictal myoclonus could be a manifestation of permanent overexcitability. © 2006 Movement Disorder Society</abstract>
<subject lang="en"><genre>Keywords</genre>
<topic>Paroxysmal kinesigenic dyskinesia</topic>
<topic>myoclonus</topic>
<topic>gabapentin</topic>
<topic>channelopathies</topic>
<topic>thalamus</topic>
</subject>
<relatedItem type="host"><titleInfo><title>Movement Disorders</title>
<subTitle>Official Journal of the Movement Disorder Society</subTitle>
</titleInfo>
<titleInfo type="abbreviated"><title>Mov. Disord.</title>
</titleInfo>
<note type="content"> This article includes Supplementary Video, available online at http://www.interscience.wiley.com/jpages/0885‐3185/suppmatSupporting Info Item: Supporting Information file jws‐mds.20992.mpg - </note>
<subject><genre>article category</genre>
<topic>Brief Report</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>2006</date>
<detail type="volume"><caption>vol.</caption>
<number>21</number>
</detail>
<detail type="issue"><caption>no.</caption>
<number>9</number>
</detail>
<extent unit="pages"><start>1533</start>
<end>1535</end>
<total>3</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">B843694022D6B4CD55A6A690CCE9CA9242DE55EA</identifier>
<identifier type="DOI">10.1002/mds.20992</identifier>
<identifier type="ArticleID">MDS20992</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2006 Movement Disorder Society</accessCondition>
<recordInfo><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin>
<recordContentSource>WILEY</recordContentSource>
</recordInfo>
</mods>
</metadata>
<serie></serie>
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