Presentation of Creutzfeldt–Jakob disease as acute corticobasal degeneration syndrome
Identifieur interne : 005546 ( Main/Merge ); précédent : 005545; suivant : 005547Presentation of Creutzfeldt–Jakob disease as acute corticobasal degeneration syndrome
Auteurs : Galit Kleiner-Fisman [Canada] ; Catherine Bergeron [Canada] ; Anthony E. Lang [Canada]Source :
- Movement Disorders [ 0885-3185 ] ; 2004-08.
English descriptors
- KwdEn :
- Aged, Cerebral Cortex (metabolism), Cerebral Cortex (pathology), Creutzfeldt-Jakob Syndrome (metabolism), Creutzfeldt-Jakob Syndrome (pathology), Creutzfeldt–Jakob disease, Diffusion Magnetic Resonance Imaging (methods), Gliosis (pathology), Humans, Immunohistochemistry (methods), Male, Nerve Degeneration (metabolism), Nerve Degeneration (pathology), Prions (metabolism), Staining and Labeling (methods), corticobasal degeneration, video.
- MESH :
- chemical , metabolism : Prions.
- metabolism : Cerebral Cortex, Creutzfeldt-Jakob Syndrome, Nerve Degeneration.
- methods : Diffusion Magnetic Resonance Imaging, Immunohistochemistry, Staining and Labeling.
- pathology : Cerebral Cortex, Creutzfeldt-Jakob Syndrome, Gliosis, Nerve Degeneration.
- Aged, Humans, Male.
Abstract
We provide a brief report with videotape documentation of a possible case of Creutzfeldt–Jakob disease. © 2004 Movement Disorder Society
Url:
DOI: 10.1002/mds.20140
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