MovDisordV3, PubMed, Corpus, bibRecord, 002296

High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.

Identifieur interne : 002296 ( PubMed/Corpus ); précédent : 002295; suivant : 002297

High 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 Shang

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2008.

RBID : pubmed:18311828

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:18311828

Le 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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<sourceDesc><biblStruct><analytic><title xml:lang="en">High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.</title>
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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>
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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>
</keywords>
<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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<DateCreated><Year>2008</Year>
<Month>05</Month>
<Day>01</Day>
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<DateCompleted><Year>2008</Year>
<Month>08</Month>
<Day>06</Day>
</DateCompleted>
<DateRevised><Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1531-8257</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>23</Volume>
<Issue>6</Issue>
<PubDate><Year>2008</Year>
<Month>Apr</Month>
<Day>30</Day>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.</ArticleTitle>
<Pagination><MedlinePgn>916-7</MedlinePgn>
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<Language>eng</Language>
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<MedlineJournalInfo><Country>United States</Country>
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<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
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<ChemicalList><Chemical><RegistryNumber>E1UOL152H7</RegistryNumber>
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<Chemical><RegistryNumber>EC 1.16.3.1</RegistryNumber>
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<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D001479">Basal Ganglia</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D002353">Carrier State</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D002570">Ceruloplasmin</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006580">Heterozygote Detection</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D007501">Iron</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008279">Magnetic Resonance Imaging</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D009154">Mutation</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D012012">Red Nucleus</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D035781">Siblings</DescriptorName>
</MeshHeading>
<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>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
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</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2008</Year>
<Month>3</Month>
<Day>4</Day>
<Hour>9</Hour>
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	Movement Disorders (revue)
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Movement Disorders (revue)

High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.

High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.

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