M. Porro

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

B. Ghetti, M. Goedert, M. Spillantini, 1996, Proceedings of the National Academy of Sciences of the United States of America.

A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindred

J. Trojanowski, B. Ghetti, M. Farlow, 1993, Brain Research.

A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathies.

F. Tagliavini, M. Salmona, O. Bugiani, 1992, Biochemical and biophysical research communications.

Fatal familial insomnia

E. Scarpini, G. Macchi, F. Tagliavini, 1998, Neurology.

A Neurotoxic Prion Protein Fragment Induces Rat Astroglial Proliferation and Hypertrophy

G. Forloni, F. Tagliavini, M. Salmona, 1994, The European journal of neuroscience.

Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish Kindreds) express only PrP peptides encoded by the mutant allele

B. Ghetti, M. Farlow, F. Tagliavini, 1994, Cell.

Effectiveness of anthracycline against experimental prion disease in Syrian hamsters.

G. Forloni, F. Tagliavini, T. Bandiera, 1997, Science.

ONLY MUTANT PRP PARTICIPATES IN AMYLOID FORMATION IN GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE WITH ALA>VAL SUBSTITUTION AT CODON 117: 21

B. Ghetti, T. Bird, F. Tagliavini, 1995 .