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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Giaccone, G, Fede, G Di, Mangieri, M, Limido, L, Capobianco, R, Suardi, S, Grisoli, M, Binelli, S, Fociani, P, Bugiani, O, Tagliavini, F
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMJ Group 2007
Aiheet:
Short Report
Linkit: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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