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Milestones in atypical and secondary Parkinsonisms

Identifieur interne : 003074 ( Main/Corpus ); précédent : 003073; suivant : 003075

Milestones in atypical and secondary Parkinsonisms

Auteurs : Gregor K. Wenning ; Irene Litvan ; Eduardo Tolosa

Source :

RBID : ISTEX:E940DAB055BDBB5FD7ADF2E76897A49D2C8610D4

English descriptors

Abstract

During the last decades, atypical parkinsonian disorders such as multiple system atrophy, dementia with Lewy bodies, progressive supranuclear palsy, and corticobasal degeneration along with secondary parkinsonian disorders have been increasingly recognized as important causes of parkinsonism. Although treatment options are largely limited to date, remarkable progress has occurred through advances in the fields of molecular biology and diagnostic neuroimaging, resulting in intense preclinical drug discovery programs. Early‐investigation‐assisted clinical diagnosis has become more crucial than ever because disease‐modifying therapies will hopefully become available within this decade. © 2011 Movement Disorder Society

Url:
DOI: 10.1002/mds.23713

Links to Exploration step

ISTEX:E940DAB055BDBB5FD7ADF2E76897A49D2C8610D4

Le document en format XML

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<abstract lang="en">During the last decades, atypical parkinsonian disorders such as multiple system atrophy, dementia with Lewy bodies, progressive supranuclear palsy, and corticobasal degeneration along with secondary parkinsonian disorders have been increasingly recognized as important causes of parkinsonism. Although treatment options are largely limited to date, remarkable progress has occurred through advances in the fields of molecular biology and diagnostic neuroimaging, resulting in intense preclinical drug discovery programs. Early‐investigation‐assisted clinical diagnosis has become more crucial than ever because disease‐modifying therapies will hopefully become available within this decade. © 2011 Movement Disorder Society</abstract>
<note type="content">*Relevant conflicts of interest/financial disclosures: Nothing to report.</note>
<note type="content">*Full financial disclosures and author roles may be found in the online version of this article.</note>
<subject lang="en">
<genre>Keywords</genre>
<topic>multiple system atrophy</topic>
<topic>dementia with Lewy bodies</topic>
<topic>progressive supranuclear palsy</topic>
<topic>corticobasal degeneration</topic>
<topic>secondary parkinsonism</topic>
</subject>
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<title>Movement Disorders</title>
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<titleInfo type="abbreviated">
<title>Mov. Disord.</title>
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<genre type="Journal">journal</genre>
<subject>
<genre>article category</genre>
<topic>Review</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>2011</date>
<detail type="volume">
<caption>vol.</caption>
<number>26</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>6</number>
</detail>
<extent unit="pages">
<start>1083</start>
<end>1095</end>
<total>13</total>
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<identifier type="DOI">10.1002/mds.23713</identifier>
<identifier type="ArticleID">MDS23713</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2011 Movement Disorder Society</accessCondition>
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<recordContentSource>WILEY</recordContentSource>
<recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin>
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