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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: piccardo p. J Neuropathol Exp Neurol. 2001 Dec;60(12):1137-52. doi: 10.1093/jnen/60.12.1137. J Neuropathol Exp Neurol. 2001. PMID: 11764087
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: piccardo p. 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: piccardo p. Brain Pathol. 1996 Apr;6(2):127-45. doi: 10.1111/j.1750-3639.1996.tb00796.x. Brain Pathol. 1996. PMID: 8737929 Review.
109 results