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Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.
Baiardi S, Rossi M, Mammana A, Appleby BS, Barria MA, Calì I, Gambetti P, Gelpi E, Giese A, Ghetti B, Herms J, Ladogana A, Mikol J, Pal S, Ritchie DL, Ruf V, Windl O, Capellari S, Parchi P. Baiardi S, et al. Among authors: gambetti p. Acta Neuropathol. 2021 Oct;142(4):707-728. doi: 10.1007/s00401-021-02350-y. Epub 2021 Jul 29. Acta Neuropathol. 2021. PMID: 34324063 Free PMC article.
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 …
Variant Creutzfeldt-Jakob disease: French versus British.
Zou WQ, Gambetti P. Zou WQ, et al. Among authors: gambetti p. Ann Neurol. 2009 Mar;65(3):233-5. doi: 10.1002/ana.21637. Ann Neurol. 2009. PMID: 19334065 Free PMC article. No abstract available.
353 results