Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for GCH1 mutations
Identifieur interne : 003976 ( Istex/Corpus ); précédent : 003975; suivant : 003977Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for GCH1 mutations
Auteurs : Yoshiaki Furukawa ; James J. Filiano ; Stephen J. KishSource :
- Movement Disorders [ 0885-3185 ] ; 2004-10.
English descriptors
Abstract
Amantadine suppressed severe levodopa‐induced choreic dyskinesia, which developed at initiation of levodopa therapy, in two siblings manifesting dystonia with motor delay phenotype of GTP cyclohydrolase I deficiency caused by compound heterozygous GCH1 mutations. Our finding suggests a beneficial effect of amantadine on this type of dyskinesia frequently observed in relatively severe dopamine‐deficient metabolic disorders. © 2004 Movement Disorder Society
Url:
DOI: 10.1002/mds.20194
Links to Exploration step
ISTEX:19E87E9E42A5799A024DE5A9F3F2BA61D713A376Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for GCH1 mutations</title>
<author><name sortKey="Furukawa, Yoshiaki" sort="Furukawa, Yoshiaki" uniqKey="Furukawa Y" first="Yoshiaki" last="Furukawa">Yoshiaki Furukawa</name>
<affiliation><mods:affiliation>Movement Disorders Research Laboratory, Centre for Addiction and Mental Health‐Clarke Division, Toronto, Ontario, Canada</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Filiano, James J" sort="Filiano, James J" uniqKey="Filiano J" first="James J." last="Filiano">James J. Filiano</name>
<affiliation><mods:affiliation>Department of Pediatrics/Neurology, Dartmouth–Hitchcock Medical Center, Lebanon, New Hampshire, USA</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Kish, Stephen J" sort="Kish, Stephen J" uniqKey="Kish S" first="Stephen J." last="Kish">Stephen J. Kish</name>
<affiliation><mods:affiliation>Human Neurochemical Pathology Laboratory, Centre for Addiction and Mental Health—Clarke Division, Toronto, Ontario, Canada</mods:affiliation>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:19E87E9E42A5799A024DE5A9F3F2BA61D713A376</idno>
<date when="2004" year="2004">2004</date>
<idno type="doi">10.1002/mds.20194</idno>
<idno type="url">https://api.istex.fr/document/19E87E9E42A5799A024DE5A9F3F2BA61D713A376/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">003976</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for GCH1 mutations</title>
<author><name sortKey="Furukawa, Yoshiaki" sort="Furukawa, Yoshiaki" uniqKey="Furukawa Y" first="Yoshiaki" last="Furukawa">Yoshiaki Furukawa</name>
<affiliation><mods:affiliation>Movement Disorders Research Laboratory, Centre for Addiction and Mental Health‐Clarke Division, Toronto, Ontario, Canada</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Filiano, James J" sort="Filiano, James J" uniqKey="Filiano J" first="James J." last="Filiano">James J. Filiano</name>
<affiliation><mods:affiliation>Department of Pediatrics/Neurology, Dartmouth–Hitchcock Medical Center, Lebanon, New Hampshire, USA</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Kish, Stephen J" sort="Kish, Stephen J" uniqKey="Kish S" first="Stephen J." last="Kish">Stephen J. Kish</name>
<affiliation><mods:affiliation>Human Neurochemical Pathology Laboratory, Centre for Addiction and Mental Health—Clarke Division, Toronto, Ontario, Canada</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>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2004-10">2004-10</date>
<biblScope unit="vol">19</biblScope>
<biblScope unit="issue">10</biblScope>
<biblScope unit="page" from="1256">1256</biblScope>
<biblScope unit="page" to="1258">1258</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">19E87E9E42A5799A024DE5A9F3F2BA61D713A376</idno>
<idno type="DOI">10.1002/mds.20194</idno>
<idno type="ArticleID">MDS20194</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>GTP cyclohydrolase I deficiency</term>
<term>amantadine</term>
<term>levodopa‐induced dyskinesias</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Amantadine suppressed severe levodopa‐induced choreic dyskinesia, which developed at initiation of levodopa therapy, in two siblings manifesting dystonia with motor delay phenotype of GTP cyclohydrolase I deficiency caused by compound heterozygous GCH1 mutations. Our finding suggests a beneficial effect of amantadine on this type of dyskinesia frequently observed in relatively severe dopamine‐deficient metabolic disorders. © 2004 Movement Disorder Society</div>
</front>
</TEI>
<istex><corpusName>wiley</corpusName>
<author><json:item><name>Yoshiaki Furukawa MD</name>
<affiliations><json:string>Movement Disorders Research Laboratory, Centre for Addiction and Mental Health‐Clarke Division, Toronto, Ontario, Canada</json:string>
</affiliations>
</json:item>
<json:item><name>James J. Filiano MD</name>
<affiliations><json:string>Department of Pediatrics/Neurology, Dartmouth–Hitchcock Medical Center, Lebanon, New Hampshire, USA</json:string>
</affiliations>
</json:item>
<json:item><name>Stephen J. Kish PhD</name>
<affiliations><json:string>Human Neurochemical Pathology Laboratory, Centre for Addiction and Mental Health—Clarke Division, Toronto, Ontario, Canada</json:string>
</affiliations>
</json:item>
</author>
<subject><json:item><lang><json:string>eng</json:string>
</lang>
<value>amantadine</value>
</json:item>
<json:item><lang><json:string>eng</json:string>
</lang>
<value>levodopa‐induced dyskinesias</value>
</json:item>
<json:item><lang><json:string>eng</json:string>
</lang>
<value>GTP cyclohydrolase I deficiency</value>
</json:item>
</subject>
<language><json:string>eng</json:string>
</language>
<abstract>Amantadine suppressed severe levodopa‐induced choreic dyskinesia, which developed at initiation of levodopa therapy, in two siblings manifesting dystonia with motor delay phenotype of GTP cyclohydrolase I deficiency caused by compound heterozygous GCH1 mutations. Our finding suggests a beneficial effect of amantadine on this type of dyskinesia frequently observed in relatively severe dopamine‐deficient metabolic disorders. © 2004 Movement Disorder Society</abstract>
<qualityIndicators><score>2.318</score>
<pdfVersion>1.3</pdfVersion>
<pdfPageSize>612 x 810 pts</pdfPageSize>
<refBibsNative>true</refBibsNative>
<abstractCharCount>459</abstractCharCount>
<pdfWordCount>1610</pdfWordCount>
<pdfCharCount>11205</pdfCharCount>
<pdfPageCount>3</pdfPageCount>
<abstractWordCount>59</abstractWordCount>
</qualityIndicators>
<title>Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for GCH1 mutations</title>
<genre><json:string>Serial article</json:string>
</genre>
<host><volume>19</volume>
<pages><total>2</total>
<last>1258</last>
<first>1256</first>
</pages>
<issn><json:string>0885-3185</json:string>
</issn>
<issue>10</issue>
<subject><json:item><value>Clinical/Scientific Note</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>2004</publicationDate>
<copyrightDate>2004</copyrightDate>
<doi><json:string>10.1002/mds.20194</json:string>
</doi>
<id>19E87E9E42A5799A024DE5A9F3F2BA61D713A376</id>
<fulltext><json:item><original>true</original>
<mimetype>application/pdf</mimetype>
<extension>pdf</extension>
<uri>https://api.istex.fr/document/19E87E9E42A5799A024DE5A9F3F2BA61D713A376/fulltext/pdf</uri>
</json:item>
<json:item><original>false</original>
<mimetype>application/zip</mimetype>
<extension>zip</extension>
<uri>https://api.istex.fr/document/19E87E9E42A5799A024DE5A9F3F2BA61D713A376/fulltext/zip</uri>
</json:item>
<istex:fulltextTEI uri="https://api.istex.fr/document/19E87E9E42A5799A024DE5A9F3F2BA61D713A376/fulltext/tei"><teiHeader type="text"><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for GCH1 mutations</title>
</titleStmt>
<publicationStmt><authority>ISTEX</authority>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<availability><p>Wiley Subscription Services, Inc., A Wiley Company</p>
</availability>
<date>2004</date>
</publicationStmt>
<notesStmt><note>Centre for Addiction and Mental Health Foundation</note>
</notesStmt>
<sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for GCH1 mutations</title>
<author><persName><forename type="first">Yoshiaki</forename>
<surname>Furukawa</surname>
<roleName type="degree">MD</roleName>
</persName>
<note type="correspondence"><p>Correspondence: Movement Disorders Research Laboratory, Centre for Addiction and Mental Health—Clarke Division, 250 College Street, Toronto, Ontario M5T 1R8, Canada</p>
</note>
<affiliation>Movement Disorders Research Laboratory, Centre for Addiction and Mental Health‐Clarke Division, Toronto, Ontario, Canada</affiliation>
</author>
<author><persName><forename type="first">James J.</forename>
<surname>Filiano</surname>
<roleName type="degree">MD</roleName>
</persName>
<affiliation>Department of Pediatrics/Neurology, Dartmouth–Hitchcock Medical Center, Lebanon, New Hampshire, USA</affiliation>
</author>
<author><persName><forename type="first">Stephen J.</forename>
<surname>Kish</surname>
<roleName type="degree">PhD</roleName>
</persName>
<affiliation>Human Neurochemical Pathology Laboratory, Centre for Addiction and Mental Health—Clarke Division, Toronto, Ontario, Canada</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>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2004-10"></date>
<biblScope unit="vol">19</biblScope>
<biblScope unit="issue">10</biblScope>
<biblScope unit="page" from="1256">1256</biblScope>
<biblScope unit="page" to="1258">1258</biblScope>
</imprint>
</monogr>
<idno type="istex">19E87E9E42A5799A024DE5A9F3F2BA61D713A376</idno>
<idno type="DOI">10.1002/mds.20194</idno>
<idno type="ArticleID">MDS20194</idno>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><creation><date>2004</date>
</creation>
<langUsage><language ident="en">en</language>
</langUsage>
<abstract xml:lang="en"><p>Amantadine suppressed severe levodopa‐induced choreic dyskinesia, which developed at initiation of levodopa therapy, in two siblings manifesting dystonia with motor delay phenotype of GTP cyclohydrolase I deficiency caused by compound heterozygous GCH1 mutations. Our finding suggests a beneficial effect of amantadine on this type of dyskinesia frequently observed in relatively severe dopamine‐deficient metabolic disorders. © 2004 Movement Disorder Society</p>
</abstract>
<textClass xml:lang="en"><keywords scheme="keyword"><list><head>Keywords</head>
<item><term>amantadine</term>
</item>
<item><term>levodopa‐induced dyskinesias</term>
</item>
<item><term>GTP cyclohydrolase I deficiency</term>
</item>
</list>
</keywords>
</textClass>
<textClass><keywords scheme="Journal Subject"><list><head>Article category</head>
<item><term>Clinical/Scientific Note</term>
</item>
</list>
</keywords>
</textClass>
</profileDesc>
<revisionDesc><change when="2003-09-22">Received</change>
<change when="2004-03-22">Registration</change>
<change when="2004-10">Published</change>
</revisionDesc>
</teiHeader>
</istex:fulltextTEI>
<json:item><original>false</original>
<mimetype>text/plain</mimetype>
<extension>txt</extension>
<uri>https://api.istex.fr/document/19E87E9E42A5799A024DE5A9F3F2BA61D713A376/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>Wiley Subscription Services, Inc., A Wiley Company</publisherName>
<publisherLoc>Hoboken</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="100"><doi origin="wiley" registered="yes">10.1002/mds.v19:10</doi>
<numberingGroup><numbering type="journalVolume" number="19">19</numbering>
<numbering type="journalIssue">10</numbering>
</numberingGroup>
<coverDate startDate="2004-10">October 2004</coverDate>
</publicationMeta>
<publicationMeta level="unit" type="shortCommunication" position="260" status="forIssue"><doi origin="wiley" registered="yes">10.1002/mds.20194</doi>
<idGroup><id type="unit" value="MDS20194"></id>
</idGroup>
<countGroup><count type="pageTotal" number="2"></count>
</countGroup>
<titleGroup><title type="articleCategory">Clinical/Scientific Note</title>
<title type="tocHeading1">Clinical/Scientific Notes</title>
</titleGroup>
<copyright ownership="thirdParty">Copyright © 2004 Movement Disorder Society</copyright>
<eventGroup><event type="manuscriptReceived" date="2003-09-22"></event>
<event type="manuscriptAccepted" date="2004-03-22"></event>
<event type="publishedOnlineEarlyUnpaginated" date="2004-06-10"></event>
<event type="firstOnline" date="2004-06-10"></event>
<event type="publishedOnlineFinalForm" date="2004-09-29"></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">1256</numbering>
<numbering type="pageLast">1258</numbering>
</numberingGroup>
<correspondenceTo>Movement Disorders Research Laboratory, Centre for Addiction and Mental Health—Clarke Division, 250 College Street, Toronto, Ontario M5T 1R8, Canada</correspondenceTo>
<linkGroup><link type="toTypesetVersion" href="file:MDS.MDS20194.pdf"></link>
</linkGroup>
</publicationMeta>
<contentMeta><countGroup><count type="figureTotal" number="1"></count>
<count type="tableTotal" number="0"></count>
<count type="referenceTotal" number="15"></count>
<count type="wordTotal" number="1653"></count>
</countGroup>
<titleGroup><title type="main" xml:lang="en">Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for <i>GCH1</i>
mutations</title>
<title type="short" xml:lang="en">Clinical/Scientific Notes</title>
</titleGroup>
<creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><givenNames>Yoshiaki</givenNames>
<familyName>Furukawa</familyName>
<degrees>MD</degrees>
</personName>
<contactDetails><email>yoshiaki_furukawa@camh.net</email>
</contactDetails>
</creator>
<creator xml:id="au2" creatorRole="author" affiliationRef="#af2"><personName><givenNames>James J.</givenNames>
<familyName>Filiano</familyName>
<degrees>MD</degrees>
</personName>
</creator>
<creator xml:id="au3" creatorRole="author" affiliationRef="#af3"><personName><givenNames>Stephen J.</givenNames>
<familyName>Kish</familyName>
<degrees>PhD</degrees>
</personName>
</creator>
</creators>
<affiliationGroup><affiliation xml:id="af1" countryCode="CA" type="organization"><unparsedAffiliation>Movement Disorders Research Laboratory, Centre for Addiction and Mental Health‐Clarke Division, Toronto, Ontario, Canada</unparsedAffiliation>
</affiliation>
<affiliation xml:id="af2" countryCode="US" type="organization"><unparsedAffiliation>Department of Pediatrics/Neurology, Dartmouth–Hitchcock Medical Center, Lebanon, New Hampshire, USA</unparsedAffiliation>
</affiliation>
<affiliation xml:id="af3" countryCode="CA" type="organization"><unparsedAffiliation>Human Neurochemical Pathology Laboratory, Centre for Addiction and Mental Health—Clarke Division, Toronto, Ontario, Canada</unparsedAffiliation>
</affiliation>
</affiliationGroup>
<keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">amantadine</keyword>
<keyword xml:id="kwd2">levodopa‐induced dyskinesias</keyword>
<keyword xml:id="kwd3">GTP cyclohydrolase I deficiency</keyword>
</keywordGroup>
<fundingInfo><fundingAgency>Centre for Addiction and Mental Health Foundation</fundingAgency>
</fundingInfo>
<abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title>
<p>Amantadine suppressed severe levodopa‐induced choreic dyskinesia, which developed at initiation of levodopa therapy, in two siblings manifesting dystonia with motor delay phenotype of GTP cyclohydrolase I deficiency caused by compound heterozygous <i>GCH1</i>
mutations. Our finding suggests a beneficial effect of amantadine on this type of dyskinesia frequently observed in relatively severe dopamine‐deficient metabolic disorders. © 2004 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>Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for GCH1 mutations</title>
</titleInfo>
<titleInfo type="abbreviated" lang="en"><title>Clinical/Scientific Notes</title>
</titleInfo>
<titleInfo type="alternative" contentType="CDATA" lang="en"><title>Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for</title>
</titleInfo>
<name type="personal"><namePart type="given">Yoshiaki</namePart>
<namePart type="family">Furukawa</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Movement Disorders Research Laboratory, Centre for Addiction and Mental Health‐Clarke Division, Toronto, Ontario, Canada</affiliation>
<description>Correspondence: Movement Disorders Research Laboratory, Centre for Addiction and Mental Health—Clarke Division, 250 College Street, Toronto, Ontario M5T 1R8, Canada</description>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">James J.</namePart>
<namePart type="family">Filiano</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Pediatrics/Neurology, Dartmouth–Hitchcock Medical Center, Lebanon, New Hampshire, USA</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Stephen J.</namePart>
<namePart type="family">Kish</namePart>
<namePart type="termsOfAddress">PhD</namePart>
<affiliation>Human Neurochemical Pathology Laboratory, Centre for Addiction and Mental Health—Clarke Division, Toronto, Ontario, Canada</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<typeOfResource>text</typeOfResource>
<genre authority="originalCategForm">shortCommunication</genre>
<originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<place><placeTerm type="text">Hoboken</placeTerm>
</place>
<dateIssued encoding="w3cdtf">2004-10</dateIssued>
<dateCaptured encoding="w3cdtf">2003-09-22</dateCaptured>
<dateValid encoding="w3cdtf">2004-03-22</dateValid>
<copyrightDate encoding="w3cdtf">2004</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">15</extent>
<extent unit="words">1653</extent>
</physicalDescription>
<abstract lang="en">Amantadine suppressed severe levodopa‐induced choreic dyskinesia, which developed at initiation of levodopa therapy, in two siblings manifesting dystonia with motor delay phenotype of GTP cyclohydrolase I deficiency caused by compound heterozygous GCH1 mutations. Our finding suggests a beneficial effect of amantadine on this type of dyskinesia frequently observed in relatively severe dopamine‐deficient metabolic disorders. © 2004 Movement Disorder Society</abstract>
<note type="funding">Centre for Addiction and Mental Health Foundation</note>
<subject lang="en"><genre>Keywords</genre>
<topic>amantadine</topic>
<topic>levodopa‐induced dyskinesias</topic>
<topic>GTP cyclohydrolase I deficiency</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>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>2004</date>
<detail type="volume"><caption>vol.</caption>
<number>19</number>
</detail>
<detail type="issue"><caption>no.</caption>
<number>10</number>
</detail>
<extent unit="pages"><start>1256</start>
<end>1258</end>
<total>2</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">19E87E9E42A5799A024DE5A9F3F2BA61D713A376</identifier>
<identifier type="DOI">10.1002/mds.20194</identifier>
<identifier type="ArticleID">MDS20194</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2004 Movement Disorder Society</accessCondition>
<recordInfo><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</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 003976 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 003976 | 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:19E87E9E42A5799A024DE5A9F3F2BA61D713A376 |texte= Amantadine for levodopa‐induced choreic dyskinesia in compound heterozygotes for GCH1 mutations }}
This area was generated with Dilib version V0.6.23. |