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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Giaccone, G, Fede, G Di, Mangieri, M, Limido, L, Capobianco, R, Suardi, S, Grisoli, M, Binelli, S, Fociani, P, Bugiani, O, Tagliavini, F
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: BMJ Group 2007
विषय:
Short Report
ऑनलाइन पहुंच: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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