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Article

Classification of sporadic Creutzfeldt-Jakob disease revisited.

Brain : a journal of neurology - 1 Sept 2006

Cali Ignazio, Castellani Rudolph, Yuan Jue, Al-Shekhlee Amer, Cohen Mark L, Xiao Xiangzhu, Moleres Francisco J, Parchi Piero, Zou Wen-Quan, Gambetti Pierluigi

Abstract excerpt

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 can be MM, MV or VV. In one classification proposed by Parchi et al., [Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl...

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PMID: 16923954
DOI: 10.1093/brain/awl224

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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