Dystonia in Wilson's disease
Identifieur interne : 002E86 ( Istex/Corpus ); précédent : 002E85; suivant : 002E87Dystonia in Wilson's disease
Auteurs : Marina Svetel ; Duško Kozi ; Elka Stefanova ; Robert Semnic ; Nataša Dragaševi ; Vladimir S. KostiSource :
- Movement Disorders [ 0885-3185 ] ; 2001-07.
English descriptors
- KwdEn :
Abstract
The frequency and type of dystonic movements, as well as brain abnormalities, as depicted with magnetic resonance imaging (MRI), which might correlate with dystonia, were studied in 27 consecutive patients with a neurologic form of Wilson's disease (WD) and optimized treatment. Dystonia was found in 10 patients (37%), being generalized in half of them, while two patients had segmental, two patients multifocal dystonia, and one patient bilateral foot dystonia. Dystonia was a presenting sign in four patients and developed later in the course of the disease in six patients, despite the administered therapy for WD. Putamen was the only structure significantly more frequently lesioned in dystonic (80%) in comparison to WD patients without dystonia (24%), suggesting a relation between abnormalities in this brain region and dystonic movements in WD. © 2001 Movement Disorder Society.
Url:
DOI: 10.1002/mds.1118
Links to Exploration step
ISTEX:EA68B9EB7F07B70B244216AC469250E8F1920C14Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Dystonia in Wilson's disease</title><author><name sortKey="Svetel, Marina" sort="Svetel, Marina" uniqKey="Svetel M" first="Marina" last="Svetel">Marina Svetel</name><affiliation><mods:affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</mods:affiliation></affiliation></author><author><name sortKey="Kozi, Dusko" sort="Kozi, Dusko" uniqKey="Kozi D" first="Duško" last="Kozi">Duško Kozi</name><affiliation><mods:affiliation>MRI Center, Sremska Kamenica, Yugoslavia</mods:affiliation></affiliation></author><author><name sortKey="Stefanova, Elka" sort="Stefanova, Elka" uniqKey="Stefanova E" first="Elka" last="Stefanova">Elka Stefanova</name><affiliation><mods:affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</mods:affiliation></affiliation></author><author><name sortKey="Semnic, Robert" sort="Semnic, Robert" uniqKey="Semnic R" first="Robert" last="Semnic">Robert Semnic</name><affiliation><mods:affiliation>MRI Center, Sremska Kamenica, Yugoslavia</mods:affiliation></affiliation></author><author><name sortKey="Dragasevi, Natasa" sort="Dragasevi, Natasa" uniqKey="Dragasevi N" first="Nataša" last="Dragaševi">Nataša Dragaševi</name><affiliation><mods:affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</mods:affiliation></affiliation></author><author><name sortKey="Kosti, Vladimir S" sort="Kosti, Vladimir S" uniqKey="Kosti V" first="Vladimir S." last="Kosti">Vladimir S. Kosti</name><affiliation><mods:affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:EA68B9EB7F07B70B244216AC469250E8F1920C14</idno><date when="2001" year="2001">2001</date><idno type="doi">10.1002/mds.1118</idno><idno type="url">https://api.istex.fr/document/EA68B9EB7F07B70B244216AC469250E8F1920C14/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">002E86</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Dystonia in Wilson's disease</title><author><name sortKey="Svetel, Marina" sort="Svetel, Marina" uniqKey="Svetel M" first="Marina" last="Svetel">Marina Svetel</name><affiliation><mods:affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</mods:affiliation></affiliation></author><author><name sortKey="Kozi, Dusko" sort="Kozi, Dusko" uniqKey="Kozi D" first="Duško" last="Kozi">Duško Kozi</name><affiliation><mods:affiliation>MRI Center, Sremska Kamenica, Yugoslavia</mods:affiliation></affiliation></author><author><name sortKey="Stefanova, Elka" sort="Stefanova, Elka" uniqKey="Stefanova E" first="Elka" last="Stefanova">Elka Stefanova</name><affiliation><mods:affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</mods:affiliation></affiliation></author><author><name sortKey="Semnic, Robert" sort="Semnic, Robert" uniqKey="Semnic R" first="Robert" last="Semnic">Robert Semnic</name><affiliation><mods:affiliation>MRI Center, Sremska Kamenica, Yugoslavia</mods:affiliation></affiliation></author><author><name sortKey="Dragasevi, Natasa" sort="Dragasevi, Natasa" uniqKey="Dragasevi N" first="Nataša" last="Dragaševi">Nataša Dragaševi</name><affiliation><mods:affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</mods:affiliation></affiliation></author><author><name sortKey="Kosti, Vladimir S" sort="Kosti, Vladimir S" uniqKey="Kosti V" first="Vladimir S." last="Kosti">Vladimir S. Kosti</name><affiliation><mods:affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</mods:affiliation></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>John Wiley & Sons, Inc.</publisher><pubPlace>New York</pubPlace><date type="published" when="2001-07">2001-07</date><biblScope unit="vol">16</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="719">719</biblScope><biblScope unit="page" to="723">723</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">EA68B9EB7F07B70B244216AC469250E8F1920C14</idno><idno type="DOI">10.1002/mds.1118</idno><idno type="ArticleID">MDS1118</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>MRI</term><term>Wilson's disease</term><term>dystonia</term><term>putamen</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The frequency and type of dystonic movements, as well as brain abnormalities, as depicted with magnetic resonance imaging (MRI), which might correlate with dystonia, were studied in 27 consecutive patients with a neurologic form of Wilson's disease (WD) and optimized treatment. Dystonia was found in 10 patients (37%), being generalized in half of them, while two patients had segmental, two patients multifocal dystonia, and one patient bilateral foot dystonia. Dystonia was a presenting sign in four patients and developed later in the course of the disease in six patients, despite the administered therapy for WD. Putamen was the only structure significantly more frequently lesioned in dystonic (80%) in comparison to WD patients without dystonia (24%), suggesting a relation between abnormalities in this brain region and dystonic movements in WD. © 2001 Movement Disorder Society.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Marina Svetel MD</name><affiliations><json:string>Institute of Neurology CCS, Belgrade, Yugoslavia</json:string></affiliations></json:item><json:item><name>Duško Kozić MD</name><affiliations><json:string>MRI Center, Sremska Kamenica, Yugoslavia</json:string></affiliations></json:item><json:item><name>Elka Stefanova MD</name><affiliations><json:string>Institute of Neurology CCS, Belgrade, Yugoslavia</json:string></affiliations></json:item><json:item><name>Robert Semnic MD</name><affiliations><json:string>MRI Center, Sremska Kamenica, Yugoslavia</json:string></affiliations></json:item><json:item><name>Nataša Dragaševič MD</name><affiliations><json:string>Institute of Neurology CCS, Belgrade, Yugoslavia</json:string></affiliations></json:item><json:item><name>Vladimir S. Kostič MD</name><affiliations><json:string>Institute of Neurology CCS, Belgrade, Yugoslavia</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Wilson's disease</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>dystonia</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>MRI</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>putamen</value></json:item></subject><language><json:string>eng</json:string></language><abstract>The frequency and type of dystonic movements, as well as brain abnormalities, as depicted with magnetic resonance imaging (MRI), which might correlate with dystonia, were studied in 27 consecutive patients with a neurologic form of Wilson's disease (WD) and optimized treatment. Dystonia was found in 10 patients (37%), being generalized in half of them, while two patients had segmental, two patients multifocal dystonia, and one patient bilateral foot dystonia. Dystonia was a presenting sign in four patients and developed later in the course of the disease in six patients, despite the administered therapy for WD. Putamen was the only structure significantly more frequently lesioned in dystonic (80%) in comparison to WD patients without dystonia (24%), suggesting a relation between abnormalities in this brain region and dystonic movements in WD. © 2001 Movement Disorder Society.</abstract><qualityIndicators><score>4.126</score><pdfVersion>1.3</pdfVersion><pdfPageSize>612 x 792 pts (letter)</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>888</abstractCharCount><pdfWordCount>2518</pdfWordCount><pdfCharCount>16657</pdfCharCount><pdfPageCount>5</pdfPageCount><abstractWordCount>134</abstractWordCount></qualityIndicators><title>Dystonia in Wilson's disease</title><genre><json:string>Serial article</json:string></genre><host><volume>16</volume><pages><total>5</total><last>723</last><first>719</first></pages><issn><json:string>0885-3185</json:string></issn><issue>4</issue><subject><json:item><value>Brief Report</value></json:item></subject><genre></genre><language><json:string>unknown</json:string></language><title>Movement Disorders</title><doi><json:string>10.1002/(ISSN)1531-8257</json:string></doi></host><publicationDate>2001</publicationDate><copyrightDate>2001</copyrightDate><doi><json:string>10.1002/mds.1118</json:string></doi><id>EA68B9EB7F07B70B244216AC469250E8F1920C14</id><fulltext><json:item><original>true</original><mimetype>application/pdf</mimetype><extension>pdf</extension><uri>https://api.istex.fr/document/EA68B9EB7F07B70B244216AC469250E8F1920C14/fulltext/pdf</uri></json:item><json:item><original>false</original><mimetype>application/zip</mimetype><extension>zip</extension><uri>https://api.istex.fr/document/EA68B9EB7F07B70B244216AC469250E8F1920C14/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/EA68B9EB7F07B70B244216AC469250E8F1920C14/fulltext/tei"><teiHeader type="text"><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Dystonia in Wilson's disease</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>John Wiley & Sons, Inc.</publisher><pubPlace>New York</pubPlace><availability><p>John Wiley & Sons, Inc.</p></availability><date>2001</date></publicationStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Dystonia in Wilson's disease</title><author><persName><forename type="first">Marina</forename><surname>Svetel</surname><roleName type="degree">MD</roleName></persName><affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</affiliation></author><author><persName><forename type="first">Duško</forename><surname>Kozić</surname><roleName type="degree">MD</roleName></persName><affiliation>MRI Center, Sremska Kamenica, Yugoslavia</affiliation></author><author><persName><forename type="first">Elka</forename><surname>Stefanova</surname><roleName type="degree">MD</roleName></persName><affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</affiliation></author><author><persName><forename type="first">Robert</forename><surname>Semnic</surname><roleName type="degree">MD</roleName></persName><affiliation>MRI Center, Sremska Kamenica, Yugoslavia</affiliation></author><author><persName><forename type="first">Nataša</forename><surname>Dragaševič</surname><roleName type="degree">MD</roleName></persName><affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</affiliation></author><author><persName><forename type="first">Vladimir S.</forename><surname>Kostič</surname><roleName type="degree">MD</roleName></persName><note type="correspondence"><p>Correspondence: Institute of Neurology CCS, ul. Subotica 6, 1 1000 Belgrade, Yugoslavia</p></note><affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</affiliation></author></analytic><monogr><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="pISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><idno type="DOI">10.1002/(ISSN)1531-8257</idno><imprint><publisher>John Wiley & Sons, Inc.</publisher><pubPlace>New York</pubPlace><date type="published" when="2001-07"></date><biblScope unit="vol">16</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="719">719</biblScope><biblScope unit="page" to="723">723</biblScope></imprint></monogr><idno type="istex">EA68B9EB7F07B70B244216AC469250E8F1920C14</idno><idno type="DOI">10.1002/mds.1118</idno><idno type="ArticleID">MDS1118</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2001</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>The frequency and type of dystonic movements, as well as brain abnormalities, as depicted with magnetic resonance imaging (MRI), which might correlate with dystonia, were studied in 27 consecutive patients with a neurologic form of Wilson's disease (WD) and optimized treatment. Dystonia was found in 10 patients (37%), being generalized in half of them, while two patients had segmental, two patients multifocal dystonia, and one patient bilateral foot dystonia. Dystonia was a presenting sign in four patients and developed later in the course of the disease in six patients, despite the administered therapy for WD. Putamen was the only structure significantly more frequently lesioned in dystonic (80%) in comparison to WD patients without dystonia (24%), suggesting a relation between abnormalities in this brain region and dystonic movements in WD. © 2001 Movement Disorder Society.</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Keywords</head><item><term>Wilson's disease</term></item><item><term>dystonia</term></item><item><term>MRI</term></item><item><term>putamen</term></item></list></keywords></textClass><textClass><keywords scheme="Journal Subject"><list><head>Article category</head><item><term>Brief Report</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2000-10-06">Received</change><change when="2001-01-22">Registration</change><change when="2001-07">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/EA68B9EB7F07B70B244216AC469250E8F1920C14/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>John Wiley & Sons, Inc.</publisherName><publisherLoc>New York</publisherLoc></publisherInfo><doi registered="yes">10.1002/(ISSN)1531-8257</doi><issn type="print">0885-3185</issn><issn type="electronic">1531-8257</issn><idGroup><id type="product" value="MDS"></id></idGroup><titleGroup><title type="main" xml:lang="en" sort="MOVEMENT DISORDERS">Movement Disorders</title><title type="subtitle">Official Journal of the Movement Disorder Society</title><title type="short">Mov. Disord.</title></titleGroup></publicationMeta><publicationMeta level="part" position="40"><doi origin="wiley" registered="yes">10.1002/mds.v16:4</doi><numberingGroup><numbering type="journalVolume" number="16">16</numbering><numbering type="journalIssue">4</numbering></numberingGroup><coverDate startDate="2001-07">July 2001</coverDate></publicationMeta><publicationMeta level="unit" type="shortCommunication" position="19" status="forIssue"><doi origin="wiley" registered="yes">10.1002/mds.1118</doi><idGroup><id type="unit" value="MDS1118"></id></idGroup><countGroup><count type="pageTotal" number="5"></count></countGroup><titleGroup><title type="articleCategory">Brief Report</title><title type="tocHeading1">Brief Reports</title></titleGroup><copyright ownership="thirdParty">Copyright © 2001 Movement Disorder Society</copyright><eventGroup><event type="manuscriptReceived" date="2000-10-06"></event><event type="manuscriptRevised" date="2001-01-08"></event><event type="manuscriptAccepted" date="2001-01-22"></event><event type="publishedOnlineEarlyUnpaginated" date="2001-06-15"></event><event type="firstOnline" date="2001-06-15"></event><event type="publishedOnlineFinalForm" date="2001-07-26"></event><event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.3.2 mode:FullText source:FullText result:FullText" date="2010-03-09"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-02"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-31"></event></eventGroup><numberingGroup><numbering type="pageFirst">719</numbering><numbering type="pageLast">723</numbering></numberingGroup><correspondenceTo>Institute of Neurology CCS, ul. Subotica 6, 1 1000 Belgrade, Yugoslavia</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:MDS.MDS1118.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="1"></count><count type="tableTotal" number="3"></count><count type="referenceTotal" number="26"></count><count type="wordTotal" number="2369"></count></countGroup><titleGroup><title type="main" xml:lang="en">Dystonia in Wilson's disease</title><title type="short" xml:lang="en">Wilson's Disease and Dystonia</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Marina</givenNames><familyName>Svetel</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Duško</givenNames><familyName>Kozić</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Elka</givenNames><familyName>Stefanova</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Robert</givenNames><familyName>Semnic</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Nataša</givenNames><familyName>Dragaševič</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au6" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><givenNames>Vladimir S.</givenNames><familyName>Kostič</familyName><degrees>MD</degrees></personName><contactDetails><email>kostic@imi.bg.ac.yu</email></contactDetails></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="RS" type="organization"><unparsedAffiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</unparsedAffiliation></affiliation><affiliation xml:id="af2" type="organization"><unparsedAffiliation>MRI Center, Sremska Kamenica, Yugoslavia</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">Wilson's disease</keyword><keyword xml:id="kwd2">dystonia</keyword><keyword xml:id="kwd3">MRI</keyword><keyword xml:id="kwd4">putamen</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>The frequency and type of dystonic movements, as well as brain abnormalities, as depicted with magnetic resonance imaging (MRI), which might correlate with dystonia, were studied in 27 consecutive patients with a neurologic form of Wilson's disease (WD) and optimized treatment. Dystonia was found in 10 patients (37%), being generalized in half of them, while two patients had segmental, two patients multifocal dystonia, and one patient bilateral foot dystonia. Dystonia was a presenting sign in four patients and developed later in the course of the disease in six patients, despite the administered therapy for WD. Putamen was the only structure significantly more frequently lesioned in dystonic (80%) in comparison to WD patients without dystonia (24%), suggesting a relation between abnormalities in this brain region and dystonic movements in WD. © 2001 Movement Disorder Society.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 3-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Dystonia in Wilson's disease</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Wilson's Disease and Dystonia</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Dystonia in Wilson's disease</title></titleInfo><name type="personal"><namePart type="given">Marina</namePart><namePart type="family">Svetel</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Duško</namePart><namePart type="family">Kozić</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>MRI Center, Sremska Kamenica, Yugoslavia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Elka</namePart><namePart type="family">Stefanova</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Robert</namePart><namePart type="family">Semnic</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>MRI Center, Sremska Kamenica, Yugoslavia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Nataša</namePart><namePart type="family">Dragaševič</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Vladimir S.</namePart><namePart type="family">Kostič</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Institute of Neurology CCS, Belgrade, Yugoslavia</affiliation><description>Correspondence: Institute of Neurology CCS, ul. Subotica 6, 1 1000 Belgrade, Yugoslavia</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre authority="originalCategForm">shortCommunication</genre><originInfo><publisher>John Wiley & Sons, Inc.</publisher><place><placeTerm type="text">New York</placeTerm></place><dateIssued encoding="w3cdtf">2001-07</dateIssued><dateCaptured encoding="w3cdtf">2000-10-06</dateCaptured><dateValid encoding="w3cdtf">2001-01-22</dateValid><copyrightDate encoding="w3cdtf">2001</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="tables">3</extent><extent unit="references">26</extent><extent unit="words">2369</extent></physicalDescription><abstract lang="en">The frequency and type of dystonic movements, as well as brain abnormalities, as depicted with magnetic resonance imaging (MRI), which might correlate with dystonia, were studied in 27 consecutive patients with a neurologic form of Wilson's disease (WD) and optimized treatment. Dystonia was found in 10 patients (37%), being generalized in half of them, while two patients had segmental, two patients multifocal dystonia, and one patient bilateral foot dystonia. Dystonia was a presenting sign in four patients and developed later in the course of the disease in six patients, despite the administered therapy for WD. Putamen was the only structure significantly more frequently lesioned in dystonic (80%) in comparison to WD patients without dystonia (24%), suggesting a relation between abnormalities in this brain region and dystonic movements in WD. © 2001 Movement Disorder Society.</abstract><subject lang="en"><genre>Keywords</genre><topic>Wilson's disease</topic><topic>dystonia</topic><topic>MRI</topic><topic>putamen</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><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>2001</date><detail type="volume"><caption>vol.</caption><number>16</number></detail><detail type="issue"><caption>no.</caption><number>4</number></detail><extent unit="pages"><start>719</start><end>723</end><total>5</total></extent></part></relatedItem><identifier type="istex">EA68B9EB7F07B70B244216AC469250E8F1920C14</identifier><identifier type="DOI">10.1002/mds.1118</identifier><identifier type="ArticleID">MDS1118</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2001 Movement Disorder Society</accessCondition><recordInfo><recordOrigin>John Wiley & Sons, Inc.</recordOrigin><recordContentSource>WILEY</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002E86 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 002E86 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Santé
|area= MovDisordV3
|flux= Istex
|étape= Corpus
|type= RBID
|clé= ISTEX:EA68B9EB7F07B70B244216AC469250E8F1920C14
|texte= Dystonia in Wilson's disease
}}
| This area was generated with Dilib version V0.6.23. |  |