Fabrizio Tagliavini
Fabrizio Tagliavini
Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano
Verified email at istituto-besta.it - Homepage
TitleCited byYear
Neurotoxicity of a prion protein fragment
G Forloni, N Angeretti, R Chiesa, E Monzani, M Salmona, O Bugiani, ...
Nature 362 (6420), 543, 1993
10451993
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
4642004
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
3921999
Apoptosis mediated neurotoxicity induced by chronic application of beta amyloid fragment 25-35.
G Forloni, R Chiesa, S Smiroldo, L Verga, M Salmona, F Tagliavini, ...
Neuroreport 4 (5), 523-526, 1993
3881993
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
3702000
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
3102009
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
3011988
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
2782008
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
2741993
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
2681989
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
2641996
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
2372000
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
2342001
Molecular characteristics of a protease-resistant, amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein
C Selvaggini, L Degioia, L Cantu, E Ghibaudi, L Diomede, F Passerini, ...
Biochemical and biophysical research communications 194 (3), 1380-1386, 1993
2211993
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
2211992
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
2202012
Conformational polymorphism of the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein.
L De Gioia, C Selvaggini, E Ghibaudi, L Diomede, O Bugiani, G Forloni, ...
Journal of Biological Chemistry 269 (11), 7859-7862, 1994
2131994
Evaluation of quinacrine treatment for prion diseases
A Barret, F Tagliavini, G Forloni, C Bate, M Salmona, L Colombo, ...
Journal of virology 77 (15), 8462-8469, 2003
2122003
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
2121989
Amyloid protein of Gerstmann‐Sträussler‐Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N‐terminal glycine at codon 58.
F Tagliavini, F Prelli, J Ghiso, O Bugiani, D Serban, SB Prusiner, ...
The EMBO journal 10 (3), 513-519, 1991
2061991
The system can't perform the operation now. Try again later.
Articles 1–20