MovDisordV3, PubMed, Corpus, bibRecord, 002798

Nigrostriatal dysfunction in X-linked dystonia-parkinsonism (DYT3).

Identifieur interne : 002798 ( PubMed/Corpus ); précédent : 002797; suivant : 002799

Nigrostriatal dysfunction in X-linked dystonia-parkinsonism (DYT3).

Auteurs : Björn Tackenberg ; Aline Metz ; Marcus Unger ; Nicole Schimke ; Sebastian Passow ; Helmut Hoeffken ; Georg F. Hoffmann ; Ulrich Müller ; Dagmar Nolte ; Wolfgang H. Oertel ; Karla Eggert ; Jens Carsten Möller

Source :

Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2007.

RBID : pubmed:17377924

English descriptors

KwdEn :
- Brain (pathology), Chromosomes, Human, X, Corpus Striatum (pathology), Corpus Striatum (radionuclide imaging), Humans, Parkinson Disease (genetics), Parkinson Disease (radionuclide imaging), Substantia Nigra (pathology), Substantia Nigra (radionuclide imaging), Tomography, Emission-Computed, Single-Photon.
MESH :
- genetics : Parkinson Disease.
- pathology : Brain, Corpus Striatum, Substantia Nigra.
- radionuclide imaging : Corpus Striatum, Parkinson Disease, Substantia Nigra.
- Chromosomes, Human, X, Humans, Tomography, Emission-Computed, Single-Photon.

DOI: 10.1002/mds.21462
PubMed: 17377924

Links to Exploration step

pubmed:17377924

Le document en format XML

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<author><name sortKey="Tackenberg, Bjorn" sort="Tackenberg, Bjorn" uniqKey="Tackenberg B" first="Björn" last="Tackenberg">Björn Tackenberg</name>
</author>
<author><name sortKey="Metz, Aline" sort="Metz, Aline" uniqKey="Metz A" first="Aline" last="Metz">Aline Metz</name>
</author>
<author><name sortKey="Unger, Marcus" sort="Unger, Marcus" uniqKey="Unger M" first="Marcus" last="Unger">Marcus Unger</name>
</author>
<author><name sortKey="Schimke, Nicole" sort="Schimke, Nicole" uniqKey="Schimke N" first="Nicole" last="Schimke">Nicole Schimke</name>
</author>
<author><name sortKey="Passow, Sebastian" sort="Passow, Sebastian" uniqKey="Passow S" first="Sebastian" last="Passow">Sebastian Passow</name>
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<author><name sortKey="Hoeffken, Helmut" sort="Hoeffken, Helmut" uniqKey="Hoeffken H" first="Helmut" last="Hoeffken">Helmut Hoeffken</name>
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<author><name sortKey="Hoffmann, Georg F" sort="Hoffmann, Georg F" uniqKey="Hoffmann G" first="Georg F" last="Hoffmann">Georg F. Hoffmann</name>
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<author><name sortKey="Muller, Ulrich" sort="Muller, Ulrich" uniqKey="Muller U" first="Ulrich" last="Müller">Ulrich Müller</name>
</author>
<author><name sortKey="Nolte, Dagmar" sort="Nolte, Dagmar" uniqKey="Nolte D" first="Dagmar" last="Nolte">Dagmar Nolte</name>
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<author><name sortKey="Oertel, Wolfgang H" sort="Oertel, Wolfgang H" uniqKey="Oertel W" first="Wolfgang H" last="Oertel">Wolfgang H. Oertel</name>
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<author><name sortKey="Eggert, Karla" sort="Eggert, Karla" uniqKey="Eggert K" first="Karla" last="Eggert">Karla Eggert</name>
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<author><name sortKey="Moller, Jens Carsten" sort="Moller, Jens Carsten" uniqKey="Moller J" first="Jens Carsten" last="Möller">Jens Carsten Möller</name>
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<term>Humans</term>
<term>Parkinson Disease (genetics)</term>
<term>Parkinson Disease (radionuclide imaging)</term>
<term>Substantia Nigra (pathology)</term>
<term>Substantia Nigra (radionuclide imaging)</term>
<term>Tomography, Emission-Computed, Single-Photon</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Parkinson Disease</term>
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<term>Corpus Striatum</term>
<term>Substantia Nigra</term>
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<keywords scheme="MESH" qualifier="radionuclide imaging" xml:lang="en"><term>Corpus Striatum</term>
<term>Parkinson Disease</term>
<term>Substantia Nigra</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Chromosomes, Human, X</term>
<term>Humans</term>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Nigrostriatal dysfunction in X-linked dystonia-parkinsonism (DYT3).</ArticleTitle>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D013378">Substantia Nigra</DescriptorName>
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<QualifierName MajorTopicYN="N" UI="Q000531">radionuclide imaging</QualifierName>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Nigrostriatal dysfunction in X-linked dystonia-parkinsonism (DYT3).

Nigrostriatal dysfunction in X-linked dystonia-parkinsonism (DYT3).

Source :

English descriptors

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki