Genetic Creutzfeldt-Jakob Disease with R208H Mutation Presenting as Progressive Supranuclear Palsy
Identifieur interne : 001113 ( Main/Exploration ); précédent : 001112; suivant : 001114Genetic Creutzfeldt-Jakob Disease with R208H Mutation Presenting as Progressive Supranuclear Palsy
Auteurs : Radoslav Matej [République tchèque, Autriche] ; Gabor G. Kovacs [Autriche] ; Silvie Johanidesova [République tchèque] ; Ji Keller [République tchèque] ; Milada Matejckova [République tchèque] ; Jana Novakova [République tchèque] ; Vladimir Sigut [République tchèque] ; Otakar Keller [République tchèque] ; Robert Rusina [République tchèque]Source :
- Movement disorders [ 0885-3185 ] ; 2012.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PascalFrancis, to step Corpus: 000234
- to stream PascalFrancis, to step Curation: 002A80
- to stream PascalFrancis, to step Checkpoint: 000186
- to stream Main, to step Merge: 001165
- to stream Main, to step Curation: 001113
Le document en format XML
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<series><title level="j" type="main">Movement disorders</title>
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<term>Mutation</term>
<term>Nervous system diseases</term>
<term>Prion</term>
<term>Supranuclear ophthalmoplegia</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Pathologie du système nerveux</term>
<term>Maladie héréditaire</term>
<term>Encéphalopathie spongiforme de Creutzfeldt-Jakob</term>
<term>Mutation</term>
<term>Ophtalmoplégie supranucléaire</term>
<term>Prion</term>
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