Spinocerebellar ataxia type 2 with levodopa‐responsive parkinsonism culminating in motor neuron disease
Identifieur interne : 000197 ( Istex/Corpus ); précédent : 000196; suivant : 000198Spinocerebellar ataxia type 2 with levodopa‐responsive parkinsonism culminating in motor neuron disease
Auteurs : Jon Infante ; José Berciano ; Victor Volpini ; Jordi Corral ; José Miguel Polo ; Julio Pascual ; Onofre CombarrosSource :
- Movement Disorders [ 0885-3185 ] ; 2004-07.
English descriptors
- KwdEn :
- ALS, SCA2, parkinsonism.
Abstract
We describe an exceptional spinocerebellar ataxia type 2 (SCA2) phenotype combining cerebellar ataxia, levodopa‐responsive parkinsonism, and motor neuron symptoms. We conclude that motor neuron symptoms and signs may be a striking manifestation in SCA2, masking pre‐existing cerebellar and extrapyramidal semeiology. © 2004 Movement Disorder Society
Url:
DOI: 10.1002/mds.20090
Links to Exploration step
ISTEX:2BA6FD2D355E3E9D873254111B9FDDCDDD0929CDLe document en format XML
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type="organization"><unparsedAffiliation>Service of Neurology, University Hospital “Marqués de Valdecilla” (University of Cantabria), Santander, Spain</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="ES" type="organization"><unparsedAffiliation>Service of Genetics, Hospital “Durán i Reynals” (IRO), Barcelona, Spain</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">SCA2</keyword><keyword xml:id="kwd2">parkinsonism</keyword><keyword xml:id="kwd3">ALS</keyword></keywordGroup><fundingInfo><fundingAgency>Investigación en Red de las Enfermedades Neurológicas</fundingAgency><fundingNumber>CO3/06</fundingNumber></fundingInfo><fundingInfo><fundingAgency>Fondo de Investigación Sanitaria</fundingAgency><fundingNumber>02/0027</fundingNumber></fundingInfo><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>We describe an exceptional spinocerebellar ataxia type 2 (SCA2) phenotype combining cerebellar ataxia, levodopa‐responsive parkinsonism, and motor neuron symptoms. We conclude that motor neuron symptoms and signs may be a striking manifestation in SCA2, masking pre‐existing cerebellar and extrapyramidal semeiology. © 2004 Movement Disorder Society</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Spinocerebellar ataxia type 2 with levodopa‐responsive parkinsonism culminating in motor neuron disease</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Clinical/Scientific Notes</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Spinocerebellar ataxia type 2 with levodopa‐responsive parkinsonism culminating in motor neuron disease</title></titleInfo><name type="personal"><namePart type="given">Jon</namePart><namePart type="family">Infante</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Service of Neurology, University Hospital “Marqués de Valdecilla” (University of Cantabria), Santander, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">José</namePart><namePart type="family">Berciano</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Service of Neurology, University Hospital “Marqués de Valdecilla” (University of Cantabria), Santander, Spain</affiliation><affiliation>Service of Neurology, University Hospital “Marqués de Valdecilla” (UC), 39008 Santander, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Victor</namePart><namePart type="family">Volpini</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Service of Genetics, Hospital “Durán i Reynals” (IRO), Barcelona, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Jordi</namePart><namePart type="family">Corral</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Service of Genetics, Hospital “Durán i Reynals” (IRO), Barcelona, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">José Miguel</namePart><namePart type="family">Polo</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Service of Neurology, University Hospital “Marqués de Valdecilla” (University of Cantabria), Santander, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Julio</namePart><namePart type="family">Pascual</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Service of Neurology, University Hospital “Marqués de Valdecilla” (University of Cantabria), Santander, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Onofre</namePart><namePart type="family">Combarros</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Service of Neurology, University Hospital “Marqués de Valdecilla” (University of Cantabria), Santander, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="brief-communication" displayLabel="shortCommunication"></genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2004-07</dateIssued><dateCaptured encoding="w3cdtf">2003-10-10</dateCaptured><dateValid encoding="w3cdtf">2003-12-29</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">3</extent><extent unit="references">35</extent><extent unit="words">3215</extent></physicalDescription><abstract lang="en">We describe an exceptional spinocerebellar ataxia type 2 (SCA2) phenotype combining cerebellar ataxia, levodopa‐responsive parkinsonism, and motor neuron symptoms. We conclude that motor neuron symptoms and signs may be a striking manifestation in SCA2, masking pre‐existing cerebellar and extrapyramidal semeiology. © 2004 Movement Disorder Society</abstract><note type="funding">Investigación en Red de las Enfermedades Neurológicas - No. CO3/06; </note><note type="funding">Fondo de Investigación Sanitaria - No. 02/0027; </note><subject lang="en"><genre>keywords</genre><topic>SCA2</topic><topic>parkinsonism</topic><topic>ALS</topic></subject><relatedItem type="host"><titleInfo><title>Movement Disorders</title></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><genre type="journal">journal</genre><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>7</number></detail><extent unit="pages"><start>848</start><end>852</end><total>5</total></extent></part></relatedItem><identifier type="istex">2BA6FD2D355E3E9D873254111B9FDDCDDD0929CD</identifier><identifier type="DOI">10.1002/mds.20090</identifier><identifier type="ArticleID">MDS20090</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2004 Movement Disorder Society</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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