Alpha‐synuclein immunohistochemistry in two cases of co‐occurring idiopathic Parkinson's disease and motor neuron disease
Identifieur interne : 003A30 ( Main/Curation ); précédent : 003A29; suivant : 003A31Alpha‐synuclein immunohistochemistry in two cases of co‐occurring idiopathic Parkinson's disease and motor neuron disease
Auteurs : Kevin J. Klos [États-Unis] ; Keith A. Josephs [États-Unis] ; Joseph E. Parisi [États-Unis] ; Dennis W. Dickson [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2005-11.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Aged, Brain (metabolism), Brain (pathology), Female, Humans, Idiopathic, Immunohistochemistry, Immunohistochemistry (methods), Lewy bodies, Lewy body, Male, Motor Neuron Disease (complications), Motor Neuron Disease (metabolism), Motor Neuron Disease (pathology), Motor neuron disease, Nervous system diseases, Neurofilament Proteins (metabolism), Parkinson Disease (complications), Parkinson Disease (metabolism), Parkinson Disease (pathology), Parkinson disease, Sporadic, Ubiquitin (metabolism), alpha-Synuclein (metabolism), argyrophilic grain disease, motor neuron disease, sporadic idiopathic Parkinson's disease.
- MESH :
- chemical , metabolism : Neurofilament Proteins, Ubiquitin, alpha-Synuclein.
- complications : Motor Neuron Disease, Parkinson Disease.
- metabolism : Brain, Motor Neuron Disease, Parkinson Disease.
- methods : Immunohistochemistry.
- pathology : Brain, Motor Neuron Disease, Parkinson Disease.
- Aged, Female, Humans, Male.
Abstract
We report on two cases of sporadic idiopathic Parkinson's disease with motor neuron disease co‐occurring in the same individuals. Pathological analysis revealed the presence of Lewy bodies in brainstem nuclei and basal forebrain consistent with Lewy body disease (LBD), as well as motor neuron degeneration and argyrophilic grain disease. We compared our two cases to all previously published pathological cases of combined LBD and motor neuron degeneration. © 2005 Movement Disorder Society
Url:
DOI: 10.1002/mds.20604
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<author><name sortKey="Parisi, Joseph E" sort="Parisi, Joseph E" uniqKey="Parisi J" first="Joseph E." last="Parisi">Joseph E. Parisi</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota</wicri:regionArea>
<placeName><region type="state">Minnesota</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Dickson, Dennis W" sort="Dickson, Dennis W" uniqKey="Dickson D" first="Dennis W." last="Dickson">Dennis W. Dickson</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neuropathology, Mayo Clinic, Jacksonville, Florida</wicri:regionArea>
<placeName><region type="state">Floride</region>
</placeName>
</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="2005-11">2005-11</date>
<biblScope unit="vol">20</biblScope>
<biblScope unit="issue">11</biblScope>
<biblScope unit="page" from="1515">1515</biblScope>
<biblScope unit="page" to="1520">1520</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">E666596F8731DB503E0C0680FF5F9ABFEB241967</idno>
<idno type="DOI">10.1002/mds.20604</idno>
<idno type="ArticleID">MDS20604</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Brain (metabolism)</term>
<term>Brain (pathology)</term>
<term>Female</term>
<term>Humans</term>
<term>Immunohistochemistry (methods)</term>
<term>Lewy bodies</term>
<term>Male</term>
<term>Motor Neuron Disease (complications)</term>
<term>Motor Neuron Disease (metabolism)</term>
<term>Motor Neuron Disease (pathology)</term>
<term>Neurofilament Proteins (metabolism)</term>
<term>Parkinson Disease (complications)</term>
<term>Parkinson Disease (metabolism)</term>
<term>Parkinson Disease (pathology)</term>
<term>Ubiquitin (metabolism)</term>
<term>alpha-Synuclein (metabolism)</term>
<term>argyrophilic grain disease</term>
<term>motor neuron disease</term>
<term>sporadic idiopathic Parkinson's disease</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Neurofilament Proteins</term>
<term>Ubiquitin</term>
<term>alpha-Synuclein</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Motor Neuron Disease</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Brain</term>
<term>Motor Neuron Disease</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Immunohistochemistry</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Brain</term>
<term>Motor Neuron Disease</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">We report on two cases of sporadic idiopathic Parkinson's disease with motor neuron disease co‐occurring in the same individuals. Pathological analysis revealed the presence of Lewy bodies in brainstem nuclei and basal forebrain consistent with Lewy body disease (LBD), as well as motor neuron degeneration and argyrophilic grain disease. We compared our two cases to all previously published pathological cases of combined LBD and motor neuron degeneration. © 2005 Movement Disorder Society</div>
</front>
</TEI>
</ISTEX>
</double>
</record>
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