Giorgio Giaccone
Giorgio Giaccone
Fondazione IRCCS Istituto Neurologica Besta
Verified email at
Cited by
Cited by
Frontotemporal Dementia and Corticobasal Degeneration in a Family with a P301S Mutation in Tau
O Bugiani, JR Murrell, G Giaccone, M Hasegawa, G Ghigo, M Tabaton, ...
Journal of neuropathology and experimental neurology 58 (6), 667-677, 1999
Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium
I Alafuzoff, T Arzberger, S Al‐Sarraj, I Bodi, N Bogdanovic, H Braak, ...
Brain pathology 18 (4), 484-496, 2008
Gerstmann‐Sträussler‐Scheinker disease II. Neurofibrillary tangles and plaques with PrP‐amyloid coexist in an affected family
B Ghetti, F Tagliavini, CL Masters, K Beyreuther, G Giaccone, L Verga, ...
Neurology 39 (11), 1453-1453, 1989
Preamyloid deposits in the cerebral cortex of patients with Alzheimer's disease and nondemented individuals
F Tagliavini, G Giaccone, B Frangione, O Bugiani
Neuroscience letters 93 (2-3), 191-196, 1988
Reviews: current concepts in Alzheimer's disease: a multidisciplinary review
L Minati, T Edginton, M Grazia Bruzzone, G Giaccone
American Journal of Alzheimer's Disease & Other Dementias® 24 (2), 95-121, 2009
Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP
B Ghetti, P Piccardo, MG Spillantini, Y Ichimiya, M Porro, F Perini, ...
Proceedings of the National Academy of Sciences 93 (2), 744-748, 1996
Down patients: extracellular preamyloid deposits precede neuritic degeneration and senile plaques
G Giaccone, F Tagliavini, G Linoli, C Bouras, L Frigerio, B Frangione, ...
Neuroscience letters 97 (1-2), 232-238, 1989
Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro
F Tagliavini, F Prelli, L Verga, G Giaccone, R Sarma, P Gorevic, B Ghetti, ...
Proceedings of the National Academy of Sciences 90 (20), 9678-9682, 1993
Glial fibrillary acidic protein and vimentin in the experimental glial reaction of the rat brain
D Schiffer, MT Giordana, A Migheli, G Giaccone, S Pezzotta, A Mauro
Brain research 374 (1), 110-118, 1986
Substitutions at codon 22 of Alzheimer's Aβ peptide induce diverse conformational changes and apoptotic effects in human cerebral endothelial cells
L Miravalle, T Tokuda, R Chiarle, G Giaccone, O Bugiani, F Tagliavini, ...
Journal of Biological Chemistry 275 (35), 27110-27116, 2000
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy
GG Kovacs, I Ferrer, LT Grinberg, I Alafuzoff, J Attems, H Budka, ...
Acta neuropathologica 131 (1), 87-102, 2016
Staging/typing of Lewy body related α-synuclein pathology: a study of the BrainNet Europe Consortium
I Alafuzoff, PG Ince, T Arzberger, S Al-Sarraj, J Bell, I Bodi, N Bogdanovic, ...
Acta neuropathologica 117 (6), 635-652, 2009
Frontotemporal dementia and its subtypes: a genome-wide association study
R Ferrari, DG Hernandez, MA Nalls, JD Rohrer, A Ramasamy, JBJ Kwok, ...
The Lancet Neurology 13 (7), 686-699, 2014
Effectiveness of anthracycline against experimental prion disease in Syrian hamsters
F Tagliavini, RA McArthur, B Canciani, G Giaccone, M Porro, M Bugiani, ...
Science 276 (5315), 1119-1121, 1997
Variably protease‐sensitive prionopathy: a new sporadic disease of the prion protein
WQ Zou, G Puoti, X Xiao, J Yuan, L Qing, I Cali, M Shimoji, ...
Annals of neurology 68 (2), 162-172, 2010
Tetracyclines affect prion infectivity
G Forloni, S Iussich, T Awan, L Colombo, N Angeretti, L Girola, I Bertani, ...
Proceedings of the National Academy of Sciences 99 (16), 10849-10854, 2002
Prion protein amyloidosis
B Ghetti, P Piccardo, B Frangione, O Bugiani, G Giaccone, K Young, ...
Brain Pathology 6 (2), 127-145, 1996
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
R Capobianco, C Casalone, S Suardi, M Mangieri, C Miccolo, L Limido, ...
PLoS Pathog 3 (3), e31, 2007
Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrPSc in the same brain
G Puoti, G Giaccone, G Rossi, B Canciani, O Bugiani, F Tagliavini
Neurology 53 (9), 2173-2173, 1999
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele
F Tagliavini, F Prelli, M Porro, G Rossi, G Giaccone, MR Farlow, ...
Cell 79 (4), 695-703, 1994
The system can't perform the operation now. Try again later.
Articles 1–20