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Classification of sporadic Creutzfeldt-Jakob disease revisited.
Cali I, Castellani R, Yuan J, Al-Shekhlee A, Cohen ML, Xiao X, Moleres FJ, Parchi P, Zou WQ, Gambetti P. Cali I, et al. Among authors: gambetti p. Brain. 2006 Sep;129(Pt 9):2266-77. doi: 10.1093/brain/awl224. Brain. 2006. PMID: 16923954
The sporadic form of Creutzfeldt-Jakob disease (sCJD) has been classified on the basis of the molecular mass of the protease-resistant scrapie prion protein (PrP(Sc)), which can be type 1 or type 2, and the genotype at the methionine (M)/valine (V) polymorphic codon 129, which ca …
The sporadic form of Creutzfeldt-Jakob disease (sCJD) has been classified on the basis of the molecular mass of the protease-resistant scrap …
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein.
Zou WQ, Puoti G, Xiao X, Yuan J, Qing L, Cali I, Shimoji M, Langeveld JP, Castellani R, Notari S, Crain B, Schmidt RE, Geschwind M, Dearmond SJ, Cairns NJ, Dickson D, Honig L, Torres JM, Mastrianni J, Capellari S, Giaccone G, Belay ED, Schonberger LB, Cohen M, Perry G, Kong Q, Parchi P, Tagliavini F, Gambetti P. Zou WQ, et al. Among authors: gambetti p. Ann Neurol. 2010 Aug;68(2):162-72. doi: 10.1002/ana.22094. Ann Neurol. 2010. PMID: 20695009 Free PMC article.
353 results