MovDisordV3, PubMed, Curation, bibRecord, 000A32

Early neuropsychiatry features in neuroferritinopathy.

Identifieur interne : 000A32 ( PubMed/Curation ); précédent : 000A31; suivant : 000A33

Early neuropsychiatry features in neuroferritinopathy.

Auteurs : Michael J. Keogh ; Baldev Singh ; Patrick F. Chinnery

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.

RBID : pubmed:23436236

English descriptors

KwdEn :
- Adult, Cognition Disorders (etiology), Female, Humans, Iron Metabolism Disorders (complications), Male, Mental Disorders (etiology), Middle Aged, Neuroaxonal Dystrophies (complications).
MESH :
- complications : Iron Metabolism Disorders, Neuroaxonal Dystrophies.
- etiology : Cognition Disorders, Mental Disorders.
- Adult, Female, Humans, Male, Middle Aged.

DOI: 10.1002/mds.25371
PubMed: 23436236

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pubmed:23436236

Le document en format XML

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<author><name sortKey="Keogh, Michael J" sort="Keogh, Michael J" uniqKey="Keogh M" first="Michael J" last="Keogh">Michael J. Keogh</name>
</author>
<author><name sortKey="Singh, Baldev" sort="Singh, Baldev" uniqKey="Singh B" first="Baldev" last="Singh">Baldev Singh</name>
</author>
<author><name sortKey="Chinnery, Patrick F" sort="Chinnery, Patrick F" uniqKey="Chinnery P" first="Patrick F" last="Chinnery">Patrick F. Chinnery</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2013">2013</date>
<idno type="doi">10.1002/mds.25371</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Early neuropsychiatry features in neuroferritinopathy.</title>
<author><name sortKey="Keogh, Michael J" sort="Keogh, Michael J" uniqKey="Keogh M" first="Michael J" last="Keogh">Michael J. Keogh</name>
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<author><name sortKey="Singh, Baldev" sort="Singh, Baldev" uniqKey="Singh B" first="Baldev" last="Singh">Baldev Singh</name>
</author>
<author><name sortKey="Chinnery, Patrick F" sort="Chinnery, Patrick F" uniqKey="Chinnery P" first="Patrick F" last="Chinnery">Patrick F. Chinnery</name>
</author>
</analytic>
<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
<imprint><date when="2013" type="published">2013</date>
</imprint>
</series>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Cognition Disorders (etiology)</term>
<term>Female</term>
<term>Humans</term>
<term>Iron Metabolism Disorders (complications)</term>
<term>Male</term>
<term>Mental Disorders (etiology)</term>
<term>Middle Aged</term>
<term>Neuroaxonal Dystrophies (complications)</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Iron Metabolism Disorders</term>
<term>Neuroaxonal Dystrophies</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Cognition Disorders</term>
<term>Mental Disorders</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
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<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">23436236</PMID>
<DateCreated><Year>2013</Year>
<Month>09</Month>
<Day>04</Day>
</DateCreated>
<DateCompleted><Year>2014</Year>
<Month>04</Month>
<Day>02</Day>
</DateCompleted>
<DateRevised><Year>2014</Year>
<Month>11</Month>
<Day>25</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1531-8257</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>28</Volume>
<Issue>9</Issue>
<PubDate><Year>2013</Year>
<Month>Aug</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Early neuropsychiatry features in neuroferritinopathy.</ArticleTitle>
<Pagination><MedlinePgn>1310-3</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/mds.25371</ELocationID>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Keogh</LastName>
<ForeName>Michael J</ForeName>
<Initials>MJ</Initials>
</Author>
<Author ValidYN="Y"><LastName>Singh</LastName>
<ForeName>Baldev</ForeName>
<Initials>B</Initials>
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<Author ValidYN="Y"><LastName>Chinnery</LastName>
<ForeName>Patrick F</ForeName>
<Initials>PF</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>096919</GrantID>
<Agency>Wellcome Trust</Agency>
<Country>United Kingdom</Country>
</Grant>
<Grant><GrantID>101876</GrantID>
<Agency>Wellcome Trust</Agency>
<Country>United Kingdom</Country>
</Grant>
<Grant><GrantID>MR/K000608/1</GrantID>
<Agency>Medical Research Council</Agency>
<Country>United Kingdom</Country>
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<PublicationTypeList><PublicationType UI="D016422">Letter</PublicationType>
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<ArticleDate DateType="Electronic"><Year>2013</Year>
<Month>02</Month>
<Day>23</Day>
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</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Mov Disord</MedlineTA>
<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
</MedlineJournalInfo>
<SupplMeshList><SupplMeshName Type="Disease" UI="C548080">Neuroferritinopathy</SupplMeshName>
</SupplMeshList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000328">Adult</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D003072">Cognition Disorders</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D019189">Iron Metabolism Disorders</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000150">complications</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D001523">Mental Disorders</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000209">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D019150">Neuroaxonal Dystrophies</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000150">complications</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2012</Year>
<Month>7</Month>
<Day>4</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised"><Year>2012</Year>
<Month>12</Month>
<Day>4</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2012</Year>
<Month>12</Month>
<Day>21</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="aheadofprint"><Year>2013</Year>
<Month>2</Month>
<Day>23</Day>
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<PubMedPubDate PubStatus="entrez"><Year>2013</Year>
<Month>2</Month>
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<Hour>6</Hour>
<Minute>0</Minute>
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<PubMedPubDate PubStatus="pubmed"><Year>2013</Year>
<Month>2</Month>
<Day>26</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2014</Year>
<Month>4</Month>
<Day>3</Day>
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<Minute>0</Minute>
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</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="doi">10.1002/mds.25371</ArticleId>
<ArticleId IdType="pubmed">23436236</ArticleId>
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</record>

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	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Movement Disorders (revue)

Early neuropsychiatry features in neuroferritinopathy.

Early neuropsychiatry features in neuroferritinopathy.

Source :

English descriptors

Links toward previous steps (curation, corpus...)

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