Focal dystonia as the presenting sign in Creutzfeldt‐Jakob disease
Identifieur interne : 004458 ( Main/Exploration ); précédent : 004457; suivant : 004459Focal dystonia as the presenting sign in Creutzfeldt‐Jakob disease
Auteurs : Mark A. Hellmann [Israël] ; Eldad Melamed [Israël]Source :
- Movement Disorders [ 0885-3185 ] ; 2002-09.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Case study, Codon, Creutzfeldt Jakob disease, Creutzfeldt-Jakob Syndrome (complications), Creutzfeldt-Jakob Syndrome (diagnosis), Creutzfeldt-Jakob Syndrome (genetics), DNA Mutational Analysis, Diagnosis, Differential, Dystonia, Dystonic Disorders (diagnosis), Dystonic Disorders (etiology), Female, Focal lesion, Frontal Lobe (pathology), Human, Humans, Inaugural sign, Magnetic Resonance Imaging, Middle Aged, Point Mutation (genetics), Prion, Severity of Illness Index.
- MESH :
- chemical : Codon.
- complications : Creutzfeldt-Jakob Syndrome.
- diagnosis : Creutzfeldt-Jakob Syndrome, Dystonic Disorders.
- etiology : Dystonic Disorders.
- genetics : Creutzfeldt-Jakob Syndrome, Point Mutation.
- pathology : Frontal Lobe.
- DNA Mutational Analysis, Diagnosis, Differential, Female, Humans, Magnetic Resonance Imaging, Middle Aged, Severity of Illness Index.
Abstract
A variety of movement disorders may occur during the course of prion disease. We describe a unique patient who had focal upper limb dystonia as the presenting symptom of familial codon 200 mutation‐positive Creutzfeldt‐Jakob disease. © 2002 Movement Disorder Society
Url:
DOI: 10.1002/mds.10232
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 001884
- to stream Istex, to step Curation: 001884
- to stream Istex, to step Checkpoint: 002D49
- to stream PubMed, to step Corpus: 003931
- to stream PubMed, to step Curation: 003931
- to stream PubMed, to step Checkpoint: 003A86
- to stream Ncbi, to step Merge: 000920
- to stream Ncbi, to step Curation: 000920
- to stream Ncbi, to step Checkpoint: 000920
- to stream Main, to step Merge: 006463
- to stream PascalFrancis, to step Corpus: 002629
- to stream PascalFrancis, to step Curation: 000692
- to stream PascalFrancis, to step Checkpoint: 002755
- to stream Main, to step Merge: 006794
- to stream Main, to step Curation: 004458
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Focal dystonia as the presenting sign in Creutzfeldt‐Jakob disease</title>
<author><name sortKey="Hellmann, Mark A" sort="Hellmann, Mark A" uniqKey="Hellmann M" first="Mark A." last="Hellmann">Mark A. Hellmann</name>
</author>
<author><name sortKey="Melamed, Eldad" sort="Melamed, Eldad" uniqKey="Melamed E" first="Eldad" last="Melamed">Eldad Melamed</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:1B04A94B3DE39111370C45AE9862F5EE600B43FF</idno>
<date when="2002" year="2002">2002</date>
<idno type="doi">10.1002/mds.10232</idno>
<idno type="url">https://api.istex.fr/document/1B04A94B3DE39111370C45AE9862F5EE600B43FF/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001884</idno>
<idno type="wicri:Area/Istex/Curation">001884</idno>
<idno type="wicri:Area/Istex/Checkpoint">002D49</idno>
<idno type="wicri:doubleKey">0885-3185:2002:Hellmann M:focal:dystonia:as</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:12360570</idno>
<idno type="wicri:Area/PubMed/Corpus">003931</idno>
<idno type="wicri:Area/PubMed/Curation">003931</idno>
<idno type="wicri:Area/PubMed/Checkpoint">003A86</idno>
<idno type="wicri:Area/Ncbi/Merge">000920</idno>
<idno type="wicri:Area/Ncbi/Curation">000920</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">000920</idno>
<idno type="wicri:doubleKey">0885-3185:2002:Hellmann M:focal:dystonia:as</idno>
<idno type="wicri:Area/Main/Merge">006463</idno>
<idno type="wicri:source">INIST</idno>
<idno type="RBID">Pascal:02-0584388</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">002629</idno>
<idno type="wicri:Area/PascalFrancis/Curation">000692</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">002755</idno>
<idno type="wicri:doubleKey">0885-3185:2002:Hellmann M:focal:dystonia:as</idno>
<idno type="wicri:Area/Main/Merge">006794</idno>
<idno type="wicri:Area/Main/Curation">004458</idno>
<idno type="wicri:Area/Main/Exploration">004458</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Focal dystonia as the presenting sign in Creutzfeldt‐Jakob disease</title>
<author><name sortKey="Hellmann, Mark A" sort="Hellmann, Mark A" uniqKey="Hellmann M" first="Mark A." last="Hellmann">Mark A. Hellmann</name>
<affiliation wicri:level="1"><country xml:lang="fr">Israël</country>
<wicri:regionArea>Department of Neurology, Rabin Medical Centre, Beilinson Campus and Tel Aviv University School of Medicine, Petah Tiqva</wicri:regionArea>
<wicri:noRegion>Petah Tiqva</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Melamed, Eldad" sort="Melamed, Eldad" uniqKey="Melamed E" first="Eldad" last="Melamed">Eldad Melamed</name>
<affiliation wicri:level="1"><country xml:lang="fr">Israël</country>
<wicri:regionArea>Department of Neurology, Rabin Medical Centre, Beilinson Campus and Tel Aviv University School of Medicine, Petah Tiqva</wicri:regionArea>
<wicri:noRegion>Petah Tiqva</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>New York</pubPlace>
<date type="published" when="2002-09">2002-09</date>
<biblScope unit="vol">17</biblScope>
<biblScope unit="issue">5</biblScope>
<biblScope unit="page" from="1097">1097</biblScope>
<biblScope unit="page" to="1098">1098</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">1B04A94B3DE39111370C45AE9862F5EE600B43FF</idno>
<idno type="DOI">10.1002/mds.10232</idno>
<idno type="ArticleID">MDS10232</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Case study</term>
<term>Codon</term>
<term>Creutzfeldt Jakob disease</term>
<term>Creutzfeldt-Jakob Syndrome (complications)</term>
<term>Creutzfeldt-Jakob Syndrome (diagnosis)</term>
<term>Creutzfeldt-Jakob Syndrome (genetics)</term>
<term>DNA Mutational Analysis</term>
<term>Diagnosis, Differential</term>
<term>Dystonia</term>
<term>Dystonic Disorders (diagnosis)</term>
<term>Dystonic Disorders (etiology)</term>
<term>Female</term>
<term>Focal lesion</term>
<term>Frontal Lobe (pathology)</term>
<term>Human</term>
<term>Humans</term>
<term>Inaugural sign</term>
<term>Magnetic Resonance Imaging</term>
<term>Middle Aged</term>
<term>Point Mutation (genetics)</term>
<term>Prion</term>
<term>Severity of Illness Index</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Codon</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Creutzfeldt-Jakob Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Creutzfeldt-Jakob Syndrome</term>
<term>Dystonic Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Dystonic Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Creutzfeldt-Jakob Syndrome</term>
<term>Point Mutation</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Frontal Lobe</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>DNA Mutational Analysis</term>
<term>Diagnosis, Differential</term>
<term>Female</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Middle Aged</term>
<term>Severity of Illness Index</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Dystonie</term>
<term>Encéphalopathie spongiforme Creutzfeldt Jakob</term>
<term>Etude cas</term>
<term>Homme</term>
<term>Lésion focale</term>
<term>Prion</term>
<term>Signe inaugural</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">A variety of movement disorders may occur during the course of prion disease. We describe a unique patient who had focal upper limb dystonia as the presenting symptom of familial codon 200 mutation‐positive Creutzfeldt‐Jakob disease. © 2002 Movement Disorder Society</div>
</front>
</TEI>
<affiliations><list><country><li>Israël</li>
</country>
</list>
<tree><country name="Israël"><noRegion><name sortKey="Hellmann, Mark A" sort="Hellmann, Mark A" uniqKey="Hellmann M" first="Mark A." last="Hellmann">Mark A. Hellmann</name>
</noRegion>
<name sortKey="Melamed, Eldad" sort="Melamed, Eldad" uniqKey="Melamed E" first="Eldad" last="Melamed">Eldad Melamed</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 004458 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 004458 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= Main |étape= Exploration |type= RBID |clé= ISTEX:1B04A94B3DE39111370C45AE9862F5EE600B43FF |texte= Focal dystonia as the presenting sign in Creutzfeldt‐Jakob disease }}
This area was generated with Dilib version V0.6.23. |