A novel phenotype of sporadic Creutzfeldt–Jakob disease

An atypical case of sporadic Creutzfeldt–Jakob disease (CJD) is described in a 78‐year‐old woman homozygous for methionine at codon 129 of the prion protein (PrP) gene. The neuropathological signature was the presence of PrP immunoreactive plaque‐like deposits in the cerebral cortex, striatum and th...

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Bibliografiske detaljer
Main Authors: Giaccone, G, Fede, G Di, Mangieri, M, Limido, L, Capobianco, R, Suardi, S, Grisoli, M, Binelli, S, Fociani, P, Bugiani, O, Tagliavini, F
Format: Artigo
Sprog:Inglês
Udgivet: BMJ Group 2007
Fag:
Short Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2095610/
https://ncbi.nlm.nih.gov/pubmed/18024694
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.2007.115444
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