Diffuse senile plaques: amorphous or fibrous?

gan Bugiani, O., Tagliavini, F., Giaccone, G., Verga, L., el-Hachimi, K., Foncin, J. F., Frangione, B.
Cyhoeddwyd 1995

Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.

gan Giaccone, G, Verga, L, Bugiani, O, Frangione, B, Serban, D, Prusiner, S B, Farlow, M R, Ghetti, B, Tagliavini, F
Cyhoeddwyd 1992

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.

gan Tagliavini, F, Prelli, F, Ghiso, J, Bugiani, O, Serban, D, Prusiner, S B, Farlow, M R, Ghetti, B, Frangione, B
Cyhoeddwyd 1991

Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro.

gan Tagliavini, F, Prelli, F, Verga, L, Giaccone, G, Sarma, R, Gorevic, P, Ghetti, B, Passerini, F, Ghibaudi, E, Forloni, G
Cyhoeddwyd 1993

A novel phenotype of sporadic Creutzfeldt–Jakob disease

gan Giaccone, G, Fede, G Di, Mangieri, M, Limido, L, Capobianco, R, Suardi, S, Grisoli, M, Binelli, S, Fociani, P, Bugiani, O, Tagliavini, F
Cyhoeddwyd 2007

Activation effects of a prion protein fragment [PrP-(106-126)] on human leucocytes.

gan Diomede, L, Sozzani, S, Luini, W, Algeri, M, De Gioia, L, Chiesa, R, Lievens, P M, Bugiani, O, Forloni, G, Tagliavini, F, Salmona, M
Cyhoeddwyd 1996

Molecular determinants of the physicochemical properties of a critical prion protein region comprising residues 106-126.

gan Salmona, M, Malesani, P, De Gioia, L, Gorla, S, Bruschi, M, Molinari, A, Della Vedova, F, Pedrotti, B, Marrari, M A, Awan, T, Bugiani, O, Forloni, G, Tagliavini, F
Cyhoeddwyd 1999

Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies

gan Tagliavini, F., Pellegrini, C., Sardone, F., Squarzoni, S., Paulsson, M., Wagener, R., Gualandi, F., Trabanelli, C., Ferlini, A., Merlini, L., Santi, S., Maraldi, N.M., Faldini, C., Sabatelli, P.
Cyhoeddwyd yn Biochim Biophys Acta (2014)

An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bo...

gan Piccardo, P., Langeveld, J. P., Hill, A. F., Dlouhy, S. R., Young, K., Giaccone, G., Rossi, G., Bugiani, M., Bugiani, O., Meloen, R. H., Collinge, J., Tagliavini, F., Ghetti, B.
Cyhoeddwyd 1998

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

gan Ghetti, B, Piccardo, P, Spillantini, M G, Ichimiya, Y, Porro, M, Perini, F, Kitamoto, T, Tateishi, J, Seiler, C, Frangione, B, Bugiani, O, Giaccone, G, Prelli, F, Goedert, M, Dlouhy, S R, Tagliavini, F
Cyhoeddwyd 1996

Differential overexpression of SERPINA3 in human prion diseases

gan Vanni, S., Moda, F., Zattoni, M., Bistaffa, E., De Cecco, E., Rossi, M., Giaccone, G., Tagliavini, F., Haïk, S., Deslys, J. P., Zanusso, G., Ironside, J. W., Ferrer, I., Kovacs, G. G., Legname, G.
Cyhoeddwyd yn Sci Rep (2017)

Evaluation of Quinacrine Treatment for Prion Diseases

gan Barret, A., Tagliavini, F., Forloni, G., Bate, C., Salmona, M., Colombo, L., De Luigi, A., Limido, L., Suardi, S., Rossi, G., Auvré, F., Adjou, K. T., Salès, N., Williams, A., Lasmézas, C., Deslys, J. P.
Cyhoeddwyd 2003

beta PP and Tau interaction. A possible link between amyloid and neurofibrillary tangles in Alzheimer's disease.

gan Giaccone, G., Pedrotti, B., Migheli, A., Verga, L., Perez, J., Racagni, G., Smith, M. A., Perry, G., De Gioia, L., Selvaggini, C., Salmona, M., Ghiso, J., Frangione, B., Islam, K., Bugiani, O., Tagliavini, F.
Cyhoeddwyd 1996