AEMV - 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. - Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP. - Proceedings of the National Academy of Sciences of the United States of America 1996 Jan 23; 93(2): 744-8
AQRU - Piccardo,P.; Tagliavini,F.; Dlouhy,S.R.; Young,K.; Seiler,C.; Rossi,G.; Hill,A.F.; Bugiani,O.; Collinge,J.; Ghetti,B. - An antiserum to residues 95-108 of human PrP detects PrPres in a variety of human and animal prion diseases - Journal of Neuropathology and Experimental Neurology 1997; 56(5): 589 Nr. 73
ASHO - Piccardo,P.; Tagliavini,F.; Dlouhy,S.R.; Young,K.; Seiler,C.; Rossi,G.; Hill,A.F.; Bugiani,M.; Bugiani,O.; Langeveld,J.P.M.; Collinge,J.; Ghetti,B. - Species and disease-specific prion protein (PrP) isoforms are detected by antibodies (abs) raised against a highly conserved mid-region sequence - Brain Pathology 1997; 7(4): 1248
AJLD - Piccardo,P.; Seiler,C.; Dlouhy,S.R.; Young,K.; Farlow,M.R.; Prelli,F.; Frangione,B.; Bugiani,O.; Tagliavini,F.; Ghetti,B. - Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred) - Journal of Neuropathology and Experimental Neurology 1996 Nov; 55(11): 1157-63
AQRV - Piccardo,P.; Seiler,C.; Dlouhy,S.; Young,K.; Farlow,M.; Prelli,F.; Frangione,B.; Bugiani,O.; Tagliavini,F.; Ghetti,B. - Proteinase-K (PK) resistant prion protein (PrP) isoforms in Gerstmann-Sträussler-Scheinker disease (GSS) F198S - Journal of Neuropathology and Experimental Neurology 1996; 55(5): 636 Nr. 125
AJLE - Piccardo,P.; Ghetti,B.; Dickson,D.W.; Vinters,H.V.; Giaccone,G.; Bugiani,O.; Tagliavini,F.; Young,K.; Dlouhy,S.R.; Seiler,C.; Jones,C.K.; Lazzarini,A.; Golbe,L.I.; Zimmermann,T.R.; Perlman,S.L.; McLachlan,D.C.; St. George-Hyslop,P.H.; Lennox,A. - Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165. - Journal of Neuropathology and Experimental Neurology 1995 Nov; 54(6): 790-801
AQRW - Piccardo,P.; Young,K.; Jones,C.K.; Seiler,C.; Lazzarini,A.; Golbe,L.I.; Zimmerman,T.R.Jr.; Dickson,D.W.; Vinters,H.V.; Lennox,A.; Perlman,S.L.; McLachlan,D.C.; St George-Hyslop,P.; Giaccone,G.; Bugiani,O.; Tagliavini,F.; Dlouhy,S.R.; Ghetti,B. - GerstmannSträussler-Scheinker (gss) disease (p102l) - prion protein (prp) core deposits are best recognized by antibodies directed to epitopes spanning prp residues 90-165 - Journal of Neuropathology and Experimental Neurology 1995; 54(3): 448 Abstraktnummer 149