Movement Disorders (revue)

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Five‐year follow‐up study of hyperechogenicity of the substantia nigra in Parkinson's disease

Identifieur interne : 003634 ( Istex/Corpus ); précédent : 003633; suivant : 003635

Five‐year follow‐up study of hyperechogenicity of the substantia nigra in Parkinson's disease

Auteurs : Daniela Berg ; Berthold Merz ; Karlheinz Reiners ; Markus Naumann ; Georg Becker

Source :

RBID : ISTEX:713284FCFD287168FFC5DE18071FF4ADC7ECB89D

English descriptors

Abstract

Using transcranial sonography, an area of hyperechogenicity at the substantia nigra (SN) may be detected as a typical marker in patients with Parkinson's disease (PD) as well as in approximately 9% of healthy subjects vulnerable to nigrostriatal impairment. In this longitudinal study, we provide evidence that the area of SN hyperechogenicity does not change in the course of PD. In conjunction with earlier findings in children and adolescents, this evidence indicates that, from late adolescence onward, this ultrasound finding is a trait marker for nigrostriatal vulnerability. © 2004 Movement Disorder Society

Url:
DOI: 10.1002/mds.20311

Links to Exploration step

ISTEX:713284FCFD287168FFC5DE18071FF4ADC7ECB89D

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<title>Five‐year follow‐up study of hyperechogenicity of the substantia nigra in Parkinson's disease</title>
</titleInfo>
<name type="personal">
<namePart type="given">Daniela</namePart>
<namePart type="family">Berg</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Institute for Medical Genetics, University of Tübingen, Tübingen, Germany</affiliation>
<affiliation>Hertie Institue for Brain Research, University of Tübingen, Tübingen, Germany</affiliation>
<description>Correspondence: Institute for Medical Genetics, Calwerstr. 7, 72076 Tübingen, Germany</description>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Berthold</namePart>
<namePart type="family">Merz</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Neurology, University of Würzburg, Würzburg, Germany</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Karlheinz</namePart>
<namePart type="family">Reiners</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Neurology, University of Würzburg, Würzburg, Germany</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Markus</namePart>
<namePart type="family">Naumann</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Neurology, University of Würzburg, Würzburg, Germany</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Georg</namePart>
<namePart type="family">Becker</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Neurology, University of Homburg/Saar, Homburg/Saar, Germany</affiliation>
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<place>
<placeTerm type="text">Hoboken</placeTerm>
</place>
<dateIssued encoding="w3cdtf">2005-03</dateIssued>
<dateCaptured encoding="w3cdtf">2004-03-28</dateCaptured>
<dateValid encoding="w3cdtf">2004-05-29</dateValid>
<copyrightDate encoding="w3cdtf">2005</copyrightDate>
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<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<abstract lang="en">Using transcranial sonography, an area of hyperechogenicity at the substantia nigra (SN) may be detected as a typical marker in patients with Parkinson's disease (PD) as well as in approximately 9% of healthy subjects vulnerable to nigrostriatal impairment. In this longitudinal study, we provide evidence that the area of SN hyperechogenicity does not change in the course of PD. In conjunction with earlier findings in children and adolescents, this evidence indicates that, from late adolescence onward, this ultrasound finding is a trait marker for nigrostriatal vulnerability. © 2004 Movement Disorder Society</abstract>
<subject lang="en">
<genre>Keywords</genre>
<topic>Parkinson's disease</topic>
<topic>transcranial sonography</topic>
<topic>hyperechogenicity of the substantia nigra</topic>
<topic>trait marker</topic>
<topic>nigrostriatal vulnerability</topic>
</subject>
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<title>Movement Disorders</title>
</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>2005</date>
<detail type="volume">
<caption>vol.</caption>
<number>20</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>3</number>
</detail>
<extent unit="pages">
<start>383</start>
<end>385</end>
<total>3</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">713284FCFD287168FFC5DE18071FF4ADC7ECB89D</identifier>
<identifier type="DOI">10.1002/mds.20311</identifier>
<identifier type="ArticleID">MDS20311</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2004 Movement Disorder Society</accessCondition>
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<recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin>
<recordContentSource>WILEY</recordContentSource>
</recordInfo>
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<serie></serie>
</istex>
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