MovDisordV3, PubMed, Corpus, bibRecord, 002D15

Creutzfeldt-Jakob disease presenting with alien limb sign.

Identifieur interne : 002D15 ( PubMed/Corpus ); précédent : 002D14; suivant : 002D16

Creutzfeldt-Jakob disease presenting with alien limb sign.

Auteurs : Brent Fogel ; Mark Wu ; Sarah Kremen ; Kolar Murthy ; George Jackson ; Zeba Vanek

Source :

Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2006.

RBID : pubmed:16552737

English descriptors

KwdEn :
- Cerebellum (pathology), Cerebral Cortex (pathology), Creutzfeldt-Jakob Syndrome (diagnosis), Creutzfeldt-Jakob Syndrome (pathology), Diagnosis, Differential, Diffusion Magnetic Resonance Imaging, Disease Progression, Dominance, Cerebral (physiology), Dystonia (diagnosis), Dystonia (etiology), Fatal Outcome, Female, Functional Laterality, Humans, Middle Aged, Neurologic Examination, Perceptual Disorders (diagnosis), Perceptual Disorders (etiology), Prions (analysis).
MESH :
- chemical , analysis : Prions.
- diagnosis : Creutzfeldt-Jakob Syndrome, Dystonia, Perceptual Disorders.
- etiology : Dystonia, Perceptual Disorders.
- pathology : Cerebellum, Cerebral Cortex, Creutzfeldt-Jakob Syndrome.
- physiology : Dominance, Cerebral.
- Diagnosis, Differential, Diffusion Magnetic Resonance Imaging, Disease Progression, Fatal Outcome, Female, Functional Laterality, Humans, Middle Aged, Neurologic Examination.

Abstract

Creutzfeldt-Jakob disease is a fatal spongiform encephalopathy, which typically presents with a rapidly progressing dementia and additional neurological findings that can be quite variable and diverse. Here we report the unusual case of a patient who presented with left alien limb sign without overt cognitive impairment and was ultimately diagnosed with pathologically confirmed Creutzfeldt-Jakob disease.

DOI: 10.1002/mds.20858
PubMed: 16552737

Links to Exploration step

pubmed:16552737

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Creutzfeldt-Jakob disease presenting with alien limb sign.</title>
<author><name sortKey="Fogel, Brent" sort="Fogel, Brent" uniqKey="Fogel B" first="Brent" last="Fogel">Brent Fogel</name>
<affiliation><nlm:affiliation>Department of Neurology, UCLA Medical Center, Los Angeles, California 90095, USA. bfogel@ucla.edu</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Wu, Mark" sort="Wu, Mark" uniqKey="Wu M" first="Mark" last="Wu">Mark Wu</name>
</author>
<author><name sortKey="Kremen, Sarah" sort="Kremen, Sarah" uniqKey="Kremen S" first="Sarah" last="Kremen">Sarah Kremen</name>
</author>
<author><name sortKey="Murthy, Kolar" sort="Murthy, Kolar" uniqKey="Murthy K" first="Kolar" last="Murthy">Kolar Murthy</name>
</author>
<author><name sortKey="Jackson, George" sort="Jackson, George" uniqKey="Jackson G" first="George" last="Jackson">George Jackson</name>
</author>
<author><name sortKey="Vanek, Zeba" sort="Vanek, Zeba" uniqKey="Vanek Z" first="Zeba" last="Vanek">Zeba Vanek</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2006">2006</date>
<idno type="doi">10.1002/mds.20858</idno>
<idno type="RBID">pubmed:16552737</idno>
<idno type="pmid">16552737</idno>
<idno type="wicri:Area/PubMed/Corpus">002D15</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Creutzfeldt-Jakob disease presenting with alien limb sign.</title>
<author><name sortKey="Fogel, Brent" sort="Fogel, Brent" uniqKey="Fogel B" first="Brent" last="Fogel">Brent Fogel</name>
<affiliation><nlm:affiliation>Department of Neurology, UCLA Medical Center, Los Angeles, California 90095, USA. bfogel@ucla.edu</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Wu, Mark" sort="Wu, Mark" uniqKey="Wu M" first="Mark" last="Wu">Mark Wu</name>
</author>
<author><name sortKey="Kremen, Sarah" sort="Kremen, Sarah" uniqKey="Kremen S" first="Sarah" last="Kremen">Sarah Kremen</name>
</author>
<author><name sortKey="Murthy, Kolar" sort="Murthy, Kolar" uniqKey="Murthy K" first="Kolar" last="Murthy">Kolar Murthy</name>
</author>
<author><name sortKey="Jackson, George" sort="Jackson, George" uniqKey="Jackson G" first="George" last="Jackson">George Jackson</name>
</author>
<author><name sortKey="Vanek, Zeba" sort="Vanek, Zeba" uniqKey="Vanek Z" first="Zeba" last="Vanek">Zeba Vanek</name>
</author>
</analytic>
<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="2006" type="published">2006</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cerebellum (pathology)</term>
<term>Cerebral Cortex (pathology)</term>
<term>Creutzfeldt-Jakob Syndrome (diagnosis)</term>
<term>Creutzfeldt-Jakob Syndrome (pathology)</term>
<term>Diagnosis, Differential</term>
<term>Diffusion Magnetic Resonance Imaging</term>
<term>Disease Progression</term>
<term>Dominance, Cerebral (physiology)</term>
<term>Dystonia (diagnosis)</term>
<term>Dystonia (etiology)</term>
<term>Fatal Outcome</term>
<term>Female</term>
<term>Functional Laterality</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Neurologic Examination</term>
<term>Perceptual Disorders (diagnosis)</term>
<term>Perceptual Disorders (etiology)</term>
<term>Prions (analysis)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Prions</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Creutzfeldt-Jakob Syndrome</term>
<term>Dystonia</term>
<term>Perceptual Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Dystonia</term>
<term>Perceptual Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Cerebellum</term>
<term>Cerebral Cortex</term>
<term>Creutzfeldt-Jakob Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Dominance, Cerebral</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Diagnosis, Differential</term>
<term>Diffusion Magnetic Resonance Imaging</term>
<term>Disease Progression</term>
<term>Fatal Outcome</term>
<term>Female</term>
<term>Functional Laterality</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Neurologic Examination</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Creutzfeldt-Jakob disease is a fatal spongiform encephalopathy, which typically presents with a rapidly progressing dementia and additional neurological findings that can be quite variable and diverse. Here we report the unusual case of a patient who presented with left alien limb sign without overt cognitive impairment and was ultimately diagnosed with pathologically confirmed Creutzfeldt-Jakob disease.</div>
</front>
</TEI>
<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">16552737</PMID>
<DateCreated><Year>2006</Year>
<Month>08</Month>
<Day>28</Day>
</DateCreated>
<DateCompleted><Year>2006</Year>
<Month>12</Month>
<Day>15</Day>
</DateCompleted>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0885-3185</ISSN>
<JournalIssue CitedMedium="Print"><Volume>21</Volume>
<Issue>7</Issue>
<PubDate><Year>2006</Year>
<Month>Jul</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Creutzfeldt-Jakob disease presenting with alien limb sign.</ArticleTitle>
<Pagination><MedlinePgn>1040-2</MedlinePgn>
</Pagination>
<Abstract><AbstractText>Creutzfeldt-Jakob disease is a fatal spongiform encephalopathy, which typically presents with a rapidly progressing dementia and additional neurological findings that can be quite variable and diverse. Here we report the unusual case of a patient who presented with left alien limb sign without overt cognitive impairment and was ultimately diagnosed with pathologically confirmed Creutzfeldt-Jakob disease.</AbstractText>
<CopyrightInformation>(c) 2006 Movement Disorder Society.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Fogel</LastName>
<ForeName>Brent</ForeName>
<Initials>B</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, UCLA Medical Center, Los Angeles, California 90095, USA. bfogel@ucla.edu</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Wu</LastName>
<ForeName>Mark</ForeName>
<Initials>M</Initials>
</Author>
<Author ValidYN="Y"><LastName>Kremen</LastName>
<ForeName>Sarah</ForeName>
<Initials>S</Initials>
</Author>
<Author ValidYN="Y"><LastName>Murthy</LastName>
<ForeName>Kolar</ForeName>
<Initials>K</Initials>
</Author>
<Author ValidYN="Y"><LastName>Jackson</LastName>
<ForeName>George</ForeName>
<Initials>G</Initials>
</Author>
<Author ValidYN="Y"><LastName>Vanek</LastName>
<ForeName>Zeba</ForeName>
<Initials>Z</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Mov Disord</MedlineTA>
<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D011328">Prions</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D002531">Cerebellum</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D002540">Cerebral Cortex</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D007562">Creutzfeldt-Jakob Syndrome</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D003937">Diagnosis, Differential</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D038524">Diffusion Magnetic Resonance Imaging</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D018450">Disease Progression</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D004292">Dominance, Cerebral</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000502">physiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D004421">Dystonia</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000209">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D017809">Fatal Outcome</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D007839">Functional Laterality</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009460">Neurologic Examination</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010468">Perceptual Disorders</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000209">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D011328">Prions</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000032">analysis</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2006</Year>
<Month>3</Month>
<Day>23</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2006</Year>
<Month>12</Month>
<Day>16</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>2006</Year>
<Month>3</Month>
<Day>23</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="doi">10.1002/mds.20858</ArticleId>
<ArticleId IdType="pubmed">16552737</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/PubMed/Corpus

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002D15 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd -nk 002D15 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    PubMed
   |étape=   Corpus
   |type=    RBID
   |clé=     pubmed:16552737
   |texte=   Creutzfeldt-Jakob disease presenting with alien limb sign.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/RBID.i   -Sk "pubmed:16552737" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd   \
       | NlmPubMed2Wicri -a MovDisordV3

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024

	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)

Creutzfeldt-Jakob disease presenting with alien limb sign.

Creutzfeldt-Jakob disease presenting with alien limb sign.

Source :

English descriptors

Abstract

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