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Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains.
PLoS One. 2008 Jul 30;3(7):e2786. doi: 10.1371/journal.pone.0002786.
PLoS One. 2008.
PMID: 18665216
Free PMC article.
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. Among authors: morain e.
Neuropathol Appl Neurobiol. 2011 Aug;37(5):500-12. doi: 10.1111/j.1365-2990.2011.01179.x.
Neuropathol Appl Neurobiol. 2011.
PMID: 21450052
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Should we still only rely on EDSS to evaluate disability in multiple sclerosis patients? A study of inter and intra rater reliability.
Cohen M, Bresch S, Thommel Rocchi O, Morain E, Benoit J, Levraut M, Fakir S, Landes C, Lebrun-Frénay C.
Cohen M, et al. Among authors: morain e.
Mult Scler Relat Disord. 2021 Sep;54:103144. doi: 10.1016/j.msard.2021.103144. Epub 2021 Jul 9.
Mult Scler Relat Disord. 2021.
PMID: 34274736
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