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Page 1
Hereditary prion protein amyloidoses.
Ghetti B, Tagliavini F, Takao M, Bugiani O, Piccardo P. Ghetti B, et al. Among authors: bugiani o. Clin Lab Med. 2003 Mar;23(1):65-85, viii. doi: 10.1016/s0272-2712(02)00064-1. Clin Lab Med. 2003. PMID: 12733425 Review.
Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations.
Piccardo P, Liepnieks JJ, William A, Dlouhy SR, Farlow MR, Young K, Nochlin D, Bird TD, Nixon RR, Ball MJ, DeCarli C, Bugiani O, Tagliavini F, Benson MD, Ghetti B. Piccardo P, et al. Among authors: bugiani o. Am J Pathol. 2001 Jun;158(6):2201-7. doi: 10.1016/S0002-9440(10)64692-5. Am J Pathol. 2001. PMID: 11395398 Free PMC article.
Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.
Ghetti B, Piccardo P, Spillantini MG, Ichimiya Y, Porro M, Perini F, Kitamoto T, Tateishi J, Seiler C, Frangione B, Bugiani O, Giaccone G, Prelli F, Goedert M, Dlouhy SR, Tagliavini F. Ghetti B, et al. Among authors: bugiani o. Proc Natl Acad Sci U S A. 1996 Jan 23;93(2):744-8. doi: 10.1073/pnas.93.2.744. Proc Natl Acad Sci U S A. 1996. PMID: 8570627 Free PMC article.
Prion protein amyloidosis.
Ghetti B, Piccardo P, Frangione B, Bugiani O, Giaccone G, Young K, Prelli F, Farlow MR, Dlouhy SR, Tagliavini F. Ghetti B, et al. Among authors: bugiani o. Brain Pathol. 1996 Apr;6(2):127-45. doi: 10.1111/j.1750-3639.1996.tb00796.x. Brain Pathol. 1996. PMID: 8737929 Review.
Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.
Piccardo P, Dlouhy SR, Lievens PM, Young K, Bird TD, Nochlin D, Dickson DW, Vinters HV, Zimmerman TR, Mackenzie IR, Kish SJ, Ang LC, De Carli C, Pocchiari M, Brown P, Gibbs CJ Jr, Gajdusek DC, Bugiani O, Ironside J, Tagliavini F, Ghetti B. Piccardo P, et al. Among authors: bugiani o. J Neuropathol Exp Neurol. 1998 Oct;57(10):979-88. doi: 10.1097/00005072-199810000-00010. J Neuropathol Exp Neurol. 1998. PMID: 9786248
Therapeutic approaches to prion diseases.
Rossi G, Salmona M, Forloni G, Bugiani O, Tagliavini F. Rossi G, et al. Among authors: bugiani o. Clin Lab Med. 2003 Mar;23(1):187-208. doi: 10.1016/s0272-2712(02)00042-2. Clin Lab Med. 2003. PMID: 12733432 Review.
Neuropathology of Gerstmann-Sträussler-Scheinker disease.
Bugiani O, Giaccone G, Piccardo P, Morbin M, Tagliavini F, Ghetti B. Bugiani O, et al. Microsc Res Tech. 2000 Jul 1;50(1):10-5. doi: 10.1002/1097-0029(20000701)50:1<10::AID-JEMT3>3.0.CO;2-6. Microsc Res Tech. 2000. PMID: 10871543 Review.
A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.
Tagliavini F, Lievens PM, Tranchant C, Warter JM, Mohr M, Giaccone G, Perini F, Rossi G, Salmona M, Piccardo P, Ghetti B, Beavis RC, Bugiani O, Frangione B, Prelli F. Tagliavini F, et al. Among authors: bugiani o. J Biol Chem. 2001 Feb 23;276(8):6009-15. doi: 10.1074/jbc.M007062200. Epub 2000 Nov 21. J Biol Chem. 2001. PMID: 11087738 Free article.
195 results