Fabrizio Tagliavini
Fabrizio Tagliavini
Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano
Verified email at - Homepage
Cited by
Cited by
Neurotoxicity of a prion protein fragment
G Forloni, N Angeretti, R Chiesa, E Monzani, M Salmona, O Bugiani, ...
Nature 362 (6420), 543-546, 1993
Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease
C Casalone, G Zanusso, P Acutis, S Ferrari, L Capucci, F Tagliavini, ...
Proceedings of the National Academy of Sciences 101 (9), 3065-3070, 2004
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis
JD Rohrer, JM Nicholas, DM Cash, J Van Swieten, E Dopper, L Jiskoot, ...
The Lancet Neurology 14 (3), 253-262, 2015
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
A recessive mutation in the APP gene with dominant-negative effect on amyloidogenesis
G Di Fede, M Catania, M Morbin, G Rossi, S Suardi, G Mazzoleni, ...
Science 323 (5920), 1473-1477, 2009
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
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy
GG Kovacs, I Ferrer, LT Grinberg, I Alafuzoff, J Attems, H Budka, ...
Acta neuropathologica 131, 87-102, 2016
Apoptosis mediated neurotoxicity induced by chronic application of β amyloid fragment 2535
G Forloni, R Chiesa, S Smiroldo, L Verga, M Salmona, F Tagliavini, ...
Neuroreport 4 (5), 523-526, 1993
Reversion of prion protein conformational changes by synthetic b-sheet breaker peptides
C Soto, RJ Kascsak, GP Saborío, P Aucouturier, T Wisniewski, F Prelli, ...
The Lancet 355 (9199), 192-197, 2000
Sporadic human prion diseases: molecular insights and diagnosis
G Puoti, A Bizzi, G Forloni, JG Safar, F Tagliavini, P Gambetti
The Lancet Neurology 11 (7), 618-628, 2012
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
Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference
AL Young, RV Marinescu, NP Oxtoby, M Bocchetta, K Yong, NC Firth, ...
Nature communications 9 (1), 4273, 2018
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
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
Anti-amyloidogenic activity of tetracyclines: studies in vitro
G Forloni, L Colombo, L Girola, F Tagliavini, M Salmona
FEBS letters 487 (3), 404-407, 2001
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
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
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
Fatal familial insomnia: clinical and pathologic study of five new cases
V Manetto, R Medori, P Cortelli, P Montagna, P Tinuper, A Baruzzi, ...
Neurology 42 (2), 312-312, 1992
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