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Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.
Faucheux BA, Morain E, Diouron V, Brandel JP, Salomon D, Sazdovitch V, Privat N, Laplanche JL, Hauw JJ, Haïk S. Faucheux BA, et al. Neuropathol Appl Neurobiol. 2011 Aug;37(5):500-12. doi: 10.1111/j.1365-2990.2011.01179.x. Neuropathol Appl Neurobiol. 2011. PMID: 21450052
Wernicke encephalopathy and Creutzfeldt-Jakob disease.
Bertrand A, Brandel JP, Grignon Y, Sazdovitch V, Seilhean D, Faucheux B, Privat N, Brault JL, Vital A, Uro-Coste E, Pluot M, Chapon F, Maurage CA, Letournel F, Vespignani H, Place G, Degos CF, Peoc'h K, Haïk S, Hauw JJ. Bertrand A, et al. J Neurol. 2009 Jun;256(6):904-9. doi: 10.1007/s00415-009-5038-1. Epub 2009 Mar 1. J Neurol. 2009. PMID: 19252796
96 results