Focal dystonia as the presenting sign in Creutzfeldt-Jakob disease
Identifieur interne : 002755 ( PascalFrancis/Checkpoint ); précédent : 002754; suivant : 002756Focal dystonia as the presenting sign in Creutzfeldt-Jakob disease
Auteurs : Mark A. Hellmann [Israël] ; Eldad Melamed [Israël]Source :
- Movement disorders [ 0885-3185 ] ; 2002.
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- Pascal (Inist)
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- topic : Homme.
English descriptors
- KwdEn :
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.
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Pascal:02-0584388Le document en format XML
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<author><name sortKey="Hellmann, Mark A" sort="Hellmann, Mark A" uniqKey="Hellmann M" first="Mark A." last="Hellmann">Mark A. Hellmann</name>
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<s2>Petah Tiqva</s2>
<s3>ISR</s3>
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<country>Israël</country>
<wicri:noRegion>Petah Tiqva</wicri:noRegion>
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<author><name sortKey="Melamed, Eldad" sort="Melamed, Eldad" uniqKey="Melamed E" first="Eldad" last="Melamed">Eldad Melamed</name>
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<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.</div>
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