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Sporadic Creutzfeldt-Jakob disease mimicking nonconvulsive status epilepticus.
Lapergue B, Demeret S, Denys V, Laplanche JL, Galanaud D, Verny M, Sazdovitch V, Baulac M, Haïk S, Hauw JJ, Bolgert F, Brandel JP, Navarro V. Lapergue B, et al. Among authors: sazdovitch v. Neurology. 2010 Jun 15;74(24):1995-9. doi: 10.1212/WNL.0b013e3181e39703. Epub 2010 May 5. Neurology. 2010. PMID: 20445151
Accuracy of diagnosis criteria in patients with suspected diagnosis of sporadic Creutzfeldt-Jakob disease and detection of 14-3-3 protein, France, 1992 to 2009.
Peckeu L, Delasnerie-Lauprètre N, Brandel JP, Salomon D, Sazdovitch V, Laplanche JL, Duyckaerts C, Seilhean D, Haïk S, Hauw JJ. Peckeu L, et al. Among authors: sazdovitch v. Euro Surveill. 2017 Oct;22(41):16-00715. doi: 10.2807/1560-7917.ES.2017.22.41.16-00715. Euro Surveill. 2017. PMID: 29043964 Free PMC article.
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. Among authors: sazdovitch v. J Neurol. 2009 Jun;256(6):904-9. doi: 10.1007/s00415-009-5038-1. Epub 2009 Mar 1. J Neurol. 2009. PMID: 19252796
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: sazdovitch v. Neuropathol Appl Neurobiol. 2011 Aug;37(5):500-12. doi: 10.1111/j.1365-2990.2011.01179.x. Neuropathol Appl Neurobiol. 2011. PMID: 21450052
76 results