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Beyond PrP res type 1/type 2 dichotomy in Creutzfeldt-Jakob disease.
Uro-Coste E, Cassard H, Simon S, Lugan S, Bilheude JM, Perret-Liaudet A, Ironside JW, Haik S, Basset-Leobon C, Lacroux C, Peoch K, Streichenberger N, Langeveld J, Head MW, Grassi J, Hauw JJ, Schelcher F, Delisle MB, Andréoletti O. Uro-Coste E, et al. PLoS Pathog. 2008 Mar;4(3):e1000029. PLoS Pathog. 2008. PMID: 18383623 Free article.
Beyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob disease.
Uro-Coste E, Cassard H, Simon S, Lugan S, Bilheude JM, Perret-Liaudet A, Ironside JW, Haik S, Basset-Leobon C, Lacroux C, Peoch' K, Streichenberger N, Langeveld J, Head MW, Grassi J, Hauw JJ, Schelcher F, Delisle MB, Andréoletti O. Uro-Coste E, et al. PLoS Pathog. 2008 Mar 14;4(3):e1000029. doi: 10.1371/journal.ppat.1000029. PLoS Pathog. 2008. PMID: 18389084 Free PMC article.
Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders.
Peoc'h K, Levavasseur E, Delmont E, De Simone A, Laffont-Proust I, Privat N, Chebaro Y, Chapuis C, Bedoucha P, Brandel JP, Laquerriere A, Kemeny JL, Hauw JJ, Borg M, Rezaei H, Derreumaux P, Laplanche JL, Haïk S. Peoc'h K, et al. Hum Mol Genet. 2012 Dec 15;21(26):5417-28. doi: 10.1093/hmg/dds377. Epub 2012 Sep 10. Hum Mol Genet. 2012. PMID: 22965875
Long-standing prion dementia manifesting as posterior cortical atrophy.
Depaz R, Haik S, Peoc'h K, Seilhean D, Grabli D, Vicart S, Sarazin M, DeToffol B, Remy C, Fallet-Bianco C, Laplanche JL, Fontaine B, Brandel JP. Depaz R, et al. Alzheimer Dis Assoc Disord. 2012 Jul-Sep;26(3):289-92. doi: 10.1097/WAD.0b013e318231e449. Alzheimer Dis Assoc Disord. 2012. PMID: 21959360
171 results