High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.
Identifieur interne : 002296 ( PubMed/Corpus ); précédent : 002295; suivant : 002297High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.
Auteurs : Qin Chen ; Xue-Ping Chen ; Ling Zou ; Dong Zhou ; Qi-Yong Gong ; Jean-Marc Burgunder ; Hui-Fang ShangSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2008.
English descriptors
- KwdEn :
- Basal Ganglia (pathology), Brain (metabolism), Brain (pathology), Carrier State, Ceruloplasmin (genetics), Female, Heterozygote Detection, Humans, Iron (metabolism), Magnetic Resonance Imaging, Male, Middle Aged, Mutation, Red Nucleus (pathology), Siblings, Substantia Nigra (pathology), Thalamus (pathology).
- MESH :
- chemical , genetics : Ceruloplasmin.
- metabolism : Brain, Iron.
- pathology : Basal Ganglia, Brain, Red Nucleus, Substantia Nigra, Thalamus.
- Carrier State, Female, Heterozygote Detection, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Mutation, Siblings.
DOI: 10.1002/mds.21980
PubMed: 18311828
Links to Exploration step
pubmed:18311828Le document en format XML
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<author><name sortKey="Chen, Qin" sort="Chen, Qin" uniqKey="Chen Q" first="Qin" last="Chen">Qin Chen</name>
</author>
<author><name sortKey="Chen, Xue Ping" sort="Chen, Xue Ping" uniqKey="Chen X" first="Xue-Ping" last="Chen">Xue-Ping Chen</name>
</author>
<author><name sortKey="Zou, Ling" sort="Zou, Ling" uniqKey="Zou L" first="Ling" last="Zou">Ling Zou</name>
</author>
<author><name sortKey="Zhou, Dong" sort="Zhou, Dong" uniqKey="Zhou D" first="Dong" last="Zhou">Dong Zhou</name>
</author>
<author><name sortKey="Gong, Qi Yong" sort="Gong, Qi Yong" uniqKey="Gong Q" first="Qi-Yong" last="Gong">Qi-Yong Gong</name>
</author>
<author><name sortKey="Burgunder, Jean Marc" sort="Burgunder, Jean Marc" uniqKey="Burgunder J" first="Jean-Marc" last="Burgunder">Jean-Marc Burgunder</name>
</author>
<author><name sortKey="Shang, Hui Fang" sort="Shang, Hui Fang" uniqKey="Shang H" first="Hui-Fang" last="Shang">Hui-Fang Shang</name>
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<author><name sortKey="Chen, Qin" sort="Chen, Qin" uniqKey="Chen Q" first="Qin" last="Chen">Qin Chen</name>
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<author><name sortKey="Chen, Xue Ping" sort="Chen, Xue Ping" uniqKey="Chen X" first="Xue-Ping" last="Chen">Xue-Ping Chen</name>
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<author><name sortKey="Zou, Ling" sort="Zou, Ling" uniqKey="Zou L" first="Ling" last="Zou">Ling Zou</name>
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<author><name sortKey="Zhou, Dong" sort="Zhou, Dong" uniqKey="Zhou D" first="Dong" last="Zhou">Dong Zhou</name>
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<author><name sortKey="Gong, Qi Yong" sort="Gong, Qi Yong" uniqKey="Gong Q" first="Qi-Yong" last="Gong">Qi-Yong Gong</name>
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<author><name sortKey="Burgunder, Jean Marc" sort="Burgunder, Jean Marc" uniqKey="Burgunder J" first="Jean-Marc" last="Burgunder">Jean-Marc Burgunder</name>
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<author><name sortKey="Shang, Hui Fang" sort="Shang, Hui Fang" uniqKey="Shang H" first="Hui-Fang" last="Shang">Hui-Fang Shang</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
<imprint><date when="2008" type="published">2008</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Basal Ganglia (pathology)</term>
<term>Brain (metabolism)</term>
<term>Brain (pathology)</term>
<term>Carrier State</term>
<term>Ceruloplasmin (genetics)</term>
<term>Female</term>
<term>Heterozygote Detection</term>
<term>Humans</term>
<term>Iron (metabolism)</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation</term>
<term>Red Nucleus (pathology)</term>
<term>Siblings</term>
<term>Substantia Nigra (pathology)</term>
<term>Thalamus (pathology)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Ceruloplasmin</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Brain</term>
<term>Iron</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Basal Ganglia</term>
<term>Brain</term>
<term>Red Nucleus</term>
<term>Substantia Nigra</term>
<term>Thalamus</term>
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<keywords scheme="MESH" xml:lang="en"><term>Carrier State</term>
<term>Female</term>
<term>Heterozygote Detection</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation</term>
<term>Siblings</term>
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<Day>01</Day>
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<DateCompleted><Year>2008</Year>
<Month>08</Month>
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<DateRevised><Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
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<JournalIssue CitedMedium="Internet"><Volume>23</Volume>
<Issue>6</Issue>
<PubDate><Year>2008</Year>
<Month>Apr</Month>
<Day>30</Day>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.</ArticleTitle>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D035781">Siblings</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D013378">Substantia Nigra</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D013788">Thalamus</DescriptorName>
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