Carregant...

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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Giaccone, G, Di Fede, Giuseppe, Mangieri, Michela, Limido, Lucia, Capobianco, Raffaella, Suardi, Silvia, Grisoli, Marina, Binelli, Simona, Fociani, Paolo, Bugiani, Orso, Tagliavini, Fabrizio
Format: Artigo
Idioma:Inglês
Publicat: BMJ Publishing Group 2009
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3029211/
https://ncbi.nlm.nih.gov/pubmed/21686549
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.09.2008.0945
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!