Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2

A 68 year old woman with sporadic Creutzfeldt-Jakob disease is described, who neither showed characteristic EEG abnormalities nor a positive test of the neuronal protein 14-3-3 or neuron specific enolase (NSE) in CSF, despite a clinical presentation with ataxia of cerebellar type, rapidly progressiv...

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Autores principales: Samman, I., Schulz-Schaeffer, W, Wohrle, J, Sommer, A, Kretzschmar, H, Hennerici, M
Formato: Artigo
Lenguaje:Inglês
Publicado: BMJ Group 1999
Materias:
Short Report
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1736619/
https://ncbi.nlm.nih.gov/pubmed/10519881
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