Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism
Identifieur interne : 003A13 ( Istex/Corpus ); précédent : 003A12; suivant : 003A14Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism
Auteurs : Federico Micheli ; María Graciela Cers Simo ; Carlos Zú Iga RamírezSource :
- Movement Disorders [ 0885-3185 ] ; 2006-05.
English descriptors
- KwdEn :
Abstract
A 47‐year‐old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment. © 2006 Movement Disorder Society
Url:
DOI: 10.1002/mds.20800
Links to Exploration step
ISTEX:2E301B3433AD4B9F6B9532DDCFA022A3AAC309CALe document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism</title><author><name sortKey="Micheli, Federico" sort="Micheli, Federico" uniqKey="Micheli F" first="Federico" last="Micheli">Federico Micheli</name><affiliation><mods:affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</mods:affiliation></affiliation></author><author><name sortKey="Cers Simo, Maria Graciela" sort="Cers Simo, Maria Graciela" uniqKey="Cers Simo M" first="María Graciela" last="Cers Simo">María Graciela Cers Simo</name><affiliation><mods:affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</mods:affiliation></affiliation></author><author><name sortKey="Zu Iga Ramirez, Carlos" sort="Zu Iga Ramirez, Carlos" uniqKey="Zu Iga Ramirez C" first="Carlos" last="Zú Iga Ramírez">Carlos Zú Iga Ramírez</name><affiliation><mods:affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA</idno><date when="2006" year="2006">2006</date><idno type="doi">10.1002/mds.20800</idno><idno type="url">https://api.istex.fr/document/2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">003A13</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism</title><author><name sortKey="Micheli, Federico" sort="Micheli, Federico" uniqKey="Micheli F" first="Federico" last="Micheli">Federico Micheli</name><affiliation><mods:affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</mods:affiliation></affiliation></author><author><name sortKey="Cers Simo, Maria Graciela" sort="Cers Simo, Maria Graciela" uniqKey="Cers Simo M" first="María Graciela" last="Cers Simo">María Graciela Cers Simo</name><affiliation><mods:affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</mods:affiliation></affiliation></author><author><name sortKey="Zu Iga Ramirez, Carlos" sort="Zu Iga Ramirez, Carlos" uniqKey="Zu Iga Ramirez C" first="Carlos" last="Zú Iga Ramírez">Carlos Zú Iga Ramírez</name><affiliation><mods:affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</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="2006-05">2006-05</date><biblScope unit="vol">21</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="716">716</biblScope><biblScope unit="page" to="717">717</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA</idno><idno type="DOI">10.1002/mds.20800</idno><idno type="ArticleID">MDS20800</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Parkinsonism</term><term>levodopa</term><term>paraparesis</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A 47‐year‐old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment. © 2006 Movement Disorder Society</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Federico Micheli MD</name><affiliations><json:string>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</json:string></affiliations></json:item><json:item><name>María Graciela Cersósimo MD</name><affiliations><json:string>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</json:string></affiliations></json:item><json:item><name>Carlos Zúñiga Ramírez MD</name><affiliations><json:string>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>paraparesis</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Parkinsonism</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>levodopa</value></json:item></subject><language><json:string>eng</json:string></language><abstract>A 47‐year‐old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment. © 2006 Movement Disorder Society</abstract><qualityIndicators><score>2.244</score><pdfVersion>1.3</pdfVersion><pdfPageSize>594 x 792 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>360</abstractCharCount><pdfWordCount>1656</pdfWordCount><pdfCharCount>10656</pdfCharCount><pdfPageCount>2</pdfPageCount><abstractWordCount>49</abstractWordCount></qualityIndicators><title>Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism</title><genre><json:string>Serial article</json:string></genre><host><volume>21</volume><pages><total>2</total><last>717</last><first>716</first></pages><issn><json:string>0885-3185</json:string></issn><issue>5</issue><subject><json:item><value>Clinical/Scientific Notes</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>2006</publicationDate><copyrightDate>2006</copyrightDate><doi><json:string>10.1002/mds.20800</json:string></doi><id>2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA</id><fulltext><json:item><original>true</original><mimetype>application/pdf</mimetype><extension>pdf</extension><uri>https://api.istex.fr/document/2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA/fulltext/pdf</uri></json:item><json:item><original>false</original><mimetype>application/zip</mimetype><extension>zip</extension><uri>https://api.istex.fr/document/2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA/fulltext/tei"><teiHeader type="text"><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism</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>2006</date></publicationStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism</title><author><persName><forename type="first">Federico</forename><surname>Micheli</surname><roleName type="degree">MD</roleName></persName><note type="correspondence"><p>Correspondence: Juncal 1695‐ P 5 Dpto J (1062), Buenos Aires, Argentina</p></note><affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</affiliation></author><author><persName><forename type="first">María Graciela</forename><surname>Cersósimo</surname><roleName type="degree">MD</roleName></persName><affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</affiliation></author><author><persName><forename type="first">Carlos</forename><surname>Zúñiga Ramírez</surname><roleName type="degree">MD</roleName></persName><affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</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="2006-05"></date><biblScope unit="vol">21</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="716">716</biblScope><biblScope unit="page" to="717">717</biblScope></imprint></monogr><idno type="istex">2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA</idno><idno type="DOI">10.1002/mds.20800</idno><idno type="ArticleID">MDS20800</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2006</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>A 47‐year‐old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment. © 2006 Movement Disorder Society</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Keywords</head><item><term>paraparesis</term></item><item><term>Parkinsonism</term></item><item><term>levodopa</term></item></list></keywords></textClass><textClass><keywords scheme="Journal Subject"><list><head>Article category</head><item><term>Clinical/Scientific Notes</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2005-06-17">Received</change><change when="2005-09-06">Registration</change><change when="2006-05">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA/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="50"><doi origin="wiley" registered="yes">10.1002/mds.v21:5</doi><numberingGroup><numbering type="journalVolume" number="21">21</numbering><numbering type="journalIssue">5</numbering></numberingGroup><coverDate startDate="2006-05">May 2006</coverDate></publicationMeta><publicationMeta level="unit" type="shortCommunication" position="230" status="forIssue"><doi origin="wiley" registered="yes">10.1002/mds.20800</doi><idGroup><id type="unit" value="MDS20800"></id></idGroup><countGroup><count type="pageTotal" number="2"></count></countGroup><titleGroup><title type="articleCategory">Clinical/Scientific Notes</title><title type="tocHeading1">Clinical/Scientific Notes</title></titleGroup><copyright ownership="thirdParty">Copyright © 2006 Movement Disorder Society</copyright><eventGroup><event type="manuscriptReceived" date="2005-06-17"></event><event type="manuscriptRevised" date="2005-08-22"></event><event type="manuscriptAccepted" date="2005-09-06"></event><event type="publishedOnlineEarlyUnpaginated" date="2006-02-06"></event><event type="firstOnline" date="2006-02-06"></event><event type="publishedOnlineFinalForm" date="2006-05-04"></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">716</numbering><numbering type="pageLast">717</numbering></numberingGroup><correspondenceTo>Juncal 1695‐ P 5 Dpto J (1062), Buenos Aires, Argentina</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:MDS.MDS20800.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="0"></count><count type="tableTotal" number="0"></count><count type="referenceTotal" number="24"></count><count type="wordTotal" number="1809"></count></countGroup><titleGroup><title type="main" xml:lang="en">Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism</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>Federico</givenNames><familyName>Micheli</familyName><degrees>MD</degrees></personName><contactDetails><email>fmicheli@fibertel.com.ar</email></contactDetails></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af1"><personName><givenNames>María Graciela</givenNames><familyName>Cersósimo</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Carlos</givenNames><familyName>Zúñiga Ramírez</familyName><degrees>MD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="AR" type="organization"><unparsedAffiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">paraparesis</keyword><keyword xml:id="kwd2">Parkinsonism</keyword><keyword xml:id="kwd3">levodopa</keyword></keywordGroup><supportingInformation><p> This article includes Supplementary Video, available online at <url href="http://www.interscience.wiley.com/jpages/0885-3185/suppmat"> http://www.interscience.wiley.com/jpages/0885‐3185/suppmat </url></p><supportingInfoItem><mediaResource alt="supporting information" href="urn-x:wiley:08853185:media:mds20800:jws-mds"></mediaResource><caption> Segment 1. (1) Baseline evaluation showing bradykinesia with slow finger tapping, postural tremor on the right hand, and hypomimia. (2) Walking with the aid of walking sticks is severely impaired. Deep tendon reflexes are brisk particularly in the lower limbs. Segment 2. (1) On L‐dopa therapy, finger tapping and gait show evident improvement. (2) Deep tendon reflexes are still brisk. Segment 3. Five years later, he developed fluctuations in motor performance and peak‐dose dyskinesias as depicted in the video clip. This video presentation has been abbreviated. The full version will appear on theMovementDisorders DVD Supplement, which is issued bi‐annually. </caption></supportingInfoItem></supportingInformation><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>A 47‐year‐old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment. © 2006 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>Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Clinical/Scientific Notes</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism</title></titleInfo><name type="personal"><namePart type="given">Federico</namePart><namePart type="family">Micheli</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</affiliation><description>Correspondence: Juncal 1695‐ P 5 Dpto J (1062), Buenos Aires, Argentina</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">María Graciela</namePart><namePart type="family">Cersósimo</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Carlos</namePart><namePart type="family">Zúñiga Ramírez</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José de San Martín, Buenos Aires, Argentina</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">2006-05</dateIssued><dateCaptured encoding="w3cdtf">2005-06-17</dateCaptured><dateValid encoding="w3cdtf">2005-09-06</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="references">24</extent><extent unit="words">1809</extent></physicalDescription><abstract lang="en">A 47‐year‐old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment. © 2006 Movement Disorder Society</abstract><subject lang="en"><genre>Keywords</genre><topic>paraparesis</topic><topic>Parkinsonism</topic><topic>levodopa</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: Segment 1. (1) Baseline evaluation showing bradykinesia with slow finger tapping, postural tremor on the right hand, and hypomimia. (2) Walking with the aid of walking sticks is severely impaired. Deep tendon reflexes are brisk particularly in the lower limbs. Segment 2. (1) On L‐dopa therapy, finger tapping and gait show evident improvement. (2) Deep tendon reflexes are still brisk. Segment 3. Five years later, he developed fluctuations in motor performance and peak‐dose dyskinesias as depicted in the video clip. This video presentation has been abbreviated. The full version will appear on theMovementDisorders DVD Supplement, which is issued bi‐annually. - </note><subject><genre>article category</genre><topic>Clinical/Scientific Notes</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>5</number></detail><extent unit="pages"><start>716</start><end>717</end><total>2</total></extent></part></relatedItem><identifier type="istex">2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA</identifier><identifier type="DOI">10.1002/mds.20800</identifier><identifier type="ArticleID">MDS20800</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></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 003A13 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 003A13 | 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:2E301B3433AD4B9F6B9532DDCFA022A3AAC309CA
|texte= Hereditary spastic paraplegia associated with dopa‐responsive parkinsonism
}}
| This area was generated with Dilib version V0.6.23. |  |