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Page 1
APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38.
Moro ML, Giaccone G, Lombardi R, Indaco A, Uggetti A, Morbin M, Saccucci S, Di Fede G, Catania M, Walsh DM, Demarchi A, Rozemuller A, Bogdanovic N, Bugiani O, Ghetti B, Tagliavini F. Moro ML, et al. Among authors: ghetti b. Acta Neuropathol. 2012 Dec;124(6):809-21. doi: 10.1007/s00401-012-1061-x. Epub 2012 Nov 13. Acta Neuropathol. 2012. PMID: 23143229
Hereditary prion protein amyloidoses.
Ghetti B, Tagliavini F, Takao M, Bugiani O, Piccardo P. Ghetti B, et al. 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.
Redox metals and oxidative abnormalities in human prion diseases.
Petersen RB, Siedlak SL, Lee HG, Kim YS, Nunomura A, Tagliavini F, Ghetti B, Cras P, Moreira PI, Castellani RJ, Guentchev M, Budka H, Ironside JW, Gambetti P, Smith MA, Perry G. Petersen RB, et al. Among authors: ghetti b. Acta Neuropathol. 2005 Sep;110(3):232-8. doi: 10.1007/s00401-005-1034-4. Epub 2005 Aug 11. Acta Neuropathol. 2005. PMID: 16096758
Chitin-like polysaccharides in Alzheimer's disease brains.
Castellani RJ, Siedlak SL, Fortino AE, Perry G, Ghetti B, Smith MA. Castellani RJ, et al. Among authors: ghetti b. Curr Alzheimer Res. 2005 Oct;2(4):419-23. doi: 10.2174/156720505774330555. Curr Alzheimer Res. 2005. PMID: 16248847
The effect of tau genotype on clinical features in FTDP-17.
Baba Y, Tsuboi Y, Baker MC, Uitti RJ, Hutton ML, Dickson DW, Farrer M, Putzke JD, Woodruff BK, Ghetti B, Murrell JR, Boeve BF, Petersen RC, Verpillat P, Brice A, Delisle MB, Rascol O, Arima K, Dysken MW, Yasuda M, Kobayashi T, Sunohara N, Komure O, Kuno S, Sperfeld AD, Stoppe G, Kohlhase J, Pickering-Brown S, Neary D, Bugiani O, Wszolek ZK. Baba Y, et al. Among authors: ghetti b. Parkinsonism Relat Disord. 2005 Jun;11(4):205-8. doi: 10.1016/j.parkreldis.2005.01.003. Parkinsonism Relat Disord. 2005. PMID: 15878580
Mutations in the tau gene (MAPT) in FTDP-17: the family with Multiple System Tauopathy with Presenile Dementia (MSTD).
Spillantini MG, Murrell JR, Goedert M, Farlow M, Klug A, Ghetti B. Spillantini MG, et al. Among authors: ghetti b. J Alzheimers Dis. 2006;9(3 Suppl):373-80. doi: 10.3233/jad-2006-9s342. J Alzheimers Dis. 2006. PMID: 16914875
The paper highlighted here [Spillantini M.G., Murrell J.R., Goedert M., Farlow M., Klug A. and Ghetti B. (1998) Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. ...
The paper highlighted here [Spillantini M.G., Murrell J.R., Goedert M., Farlow M., Klug A. and Ghetti B. (1998) Mutation in th …
583 results