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Page 1
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: bugiani o. Parkinsonism Relat Disord. 2005 Jun;11(4):205-8. doi: 10.1016/j.parkreldis.2005.01.003. Parkinsonism Relat Disord. 2005. PMID: 15878580
Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation.
Baba Y, Baker MC, Le Ber I, Brice A, Maeck L, Kohlhase J, Yasuda M, Stoppe G, Bugiani O, Sperfeld AD, Tsuboi Y, Uitti RJ, Farrer MJ, Ghetti B, Hutton ML, Wszolek ZK. Baba Y, et al. Among authors: bugiani o. J Neural Transm (Vienna). 2007 Jul;114(7):947-50. doi: 10.1007/s00702-007-0632-9. Epub 2007 Feb 23. J Neural Transm (Vienna). 2007. PMID: 17318302
Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures.
Takao M, Ghetti B, Murrell JR, Unverzagt FW, Giaccone G, Tagliavini F, Bugiani O, Piccardo P, Hulette CM, Crain BJ, Farlow MR, Heyman A. Takao M, et al. Among authors: bugiani o. J Neuropathol Exp Neurol. 2001 Dec;60(12):1137-52. doi: 10.1093/jnen/60.12.1137. J Neuropathol Exp Neurol. 2001. PMID: 11764087
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.
195 results