ATNC - Farinazzo,A.; Zanusso,G.; Piccardo,P.; Ferrari,S.; Fasoli,E.; Fiorini,M.; Gelati,M.; Prelli,F.; Frangione,B.; Rizutto,N.; Ghetti,B.; Monaco,S. - Two-dimensional analysis of Proteinase K-resistant fragments prion protein in GSS P102L mutation - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Poster Session: Genetics, strains and emerging problems GEN-28
AQDV - Ghetti,B.; Piccardo,P.; Frangione,B.; Bugiani,O.; Giaccone,G.; Young,K.; Prelli,F.; Farlow,M.R.; Dlouhy,S.R.; Tagliavini,F. - Prion protein amyloidosis (vol 6, pg 127, 1996) - Brain Pathology 1996; 6(N3): 363
AEMU - Ghetti,B.; Piccardo,P.; Frangione,B.; Bugiani,O.; Giaccone,G.; Young,K.; Prelli,F.; Farlow,M.R.; Dlouhy,S.R.; Tagliavini,F. - Prion protein amyloidosis - Brain Pathology 1996 Apr; 6(2): 127-45
AQAS - Ghetti,B.; Piccardo,P.; Frangione,B.; Bugiani,O.; Giaccone,G.; Young,K.; Prelli,F.; Farlow,M.R.; Dlouhy,S.R.; Tagliavini,F. - Prion protein hereditary amyloidosis - parenchymal and vascular - Seminars in Virology 1996; 7(N3): 189-200
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
AQDX - Ghetti,B.; Piccardo,P.; Ichimiya,Y.; Goedert,M.; Kitamoto,T.; Tateishi,J.; Spillantini,M.G.; Frangione,B.; Bugiani,O.; Giaccone,G.; Prelli,F.; Dlouhy,S.R.; et al. - Prion protein amyloid angiopathy and Alzheimer neurofibrillary tangles in prnp stop codon-145 - Journal of Neuropathology and Experimental Neurology 1995; 54(N3): 415
AGAP - Jimenez-Huete,A.; Lievens,P.M.J.; Vidal,R.; Piccardo,P.; Ghetti,B.; Tagliavini,F.; Frangione,B.; Prelli,F. - Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues - American Journal of Pathology 1998 Nov; 153(5): 1561-72
AUYP - Pankiewicz,J.; Prelli,F.; Sy,M.S.; Kascsak,R.J.; Kascsak,R.B.; Spinner,D.S.; Carp,R.I.; Meeker,H.C.; Sadowski,M.; Wisniewski,T. - Clearance and prevention of prion infection in cell culture by anti-PrP antibodies - European Journal of Neuroscience 2006 May; 23(10): 2635-47
AJJF - Perini,F.; Vidal,R.; Ghetti,B.; Tagliavini,F.; Frangione,B.; Prelli,F. - PrP27-30 is a normal soluble prion protein fragment released by human platelets - Biochemical and Biophysical Research Communications 1996 Jun 25; 223(3): 572-7
AJJG - Perini,F.; Frangione,B.; Prelli,F. - Prion protein released by platelets - Lancet 1996 Jun 8; 347(9015): 1635-6
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
APLW - Sigurdsson,E.M.; Brown,D.R.; Alim,M.A.; Scholtzova,H.; Carp,R.I.; Meeker,H.C.; Prelli,F.; Frangione,B.; Wisniewski,T. - Copper chelation delays the onset of prion disease - The Journal of Biological Chemistry 2003 Nov 21; 278(47): 46199-202
ALBG - Soto,C.; Kascsak,R.J.; Saborio,G.P.; Aucouturier,P.; Wisniewski,T.; Prelli,F.; Kascsak,R.; Mendez,E.; Harris,D.A.; Ironside,J.; Tagliavini,F.; Carp,R.I.; Frangione,B. - Reversion of prion protein conformational changes by synthetic beta-sheet breaker peptides - Lancet 2000 Jan 15; 355(9199): 192-7
ALIJ - Tagliavini,F.; Lievens,P.M.J.; Tranchant,C.; Warter,J.M.; Mohr,M.; Giaccone,G.; Perini,F.; Rossi,G.; Salmona,M.; Piccardo,P.; Ghetti,B.; Beavis,R.C.; Bugiani,O.; Frangione,B.; Prelli,F. - A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V - The Journal of Biological Chemistry 2001 Feb 23; 276(8): 6009-15
ARWK - Tagliavini,F.; Prelli,F.; Porro,M.; Rossi,G.; Giaccone,G.; Bird,T.D.; Dlouhy,S.R.; Young,K.; Piccardo,P.; Ghetti,B.; Bugiani,O.; Frangione,B. - Only mutant PrP participates in amyloid formation in Gerstmann-Sträussler-Scheinker-disease with Ala-greater-than-Val substitution at codon-117 - Journal of Neuropathology and Experimental Neurology 1995; 54(N3): 416
ALIM - Tagliavini,F.; Prelli,F.; Porro,M.; Rossi,G.; Giaccone,G.; Farlow,M.R.; Dlouhy,S.R.; Ghetti,B.; Bugiani,O.; Frangione,B. - Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele - Cell 1994 Nov 18; 79(4): 695-703
ALIN - Tagliavini,F.; Prelli,F.; Verga,L.; Giaccone,G.; Sarma,R.; Gorevic,P.; Ghetti,B.; Passerini,F.; Ghibaudi,E.; Forloni,G.; Salmona,M.; Bugiani,O.; Frangione,B. - Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro - Proceedings of the National Academy of Sciences of the United States of America 1993 Oct 15; 90(20): 9678-82
ALIO - Tagliavini,F.; Giaccone,G.; Prelli,F.; Verga,L.; Porro,M.; Trojanowski,J.Q.; Farlow,M.R.; Frangione,B.; Ghetti,B.; Bugiani,O. - A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindred - Brain Research 1993 Jul 9; 616(1-2): 325-9
ALIP - Tagliavini,F.; Prelli,F.; Porro,M.; Salmona,M.; Bugiani,O.; Frangione,B. - A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathies. - Biochemical and Biophysical Research Communications 1992 May 15; 184(3): 1398-404
ALIQ - Tagliavini,F.; Prelli,F.; Ghiso,J.; Bugiani,O.; Serban,D.; Prusiner,S.B.; Farlow,M.R.; Ghetti,B.; Frangione,B. - 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 - EMBO Journal 1991 Mar; 10(3): 513-9
AWYO - Zanusso,G.; Polo,A.; Farinazzo,A.; Nonno,R.; Cardone,F.; Di Bari,M.; Ferrari,S.; Principe,S.; Gelati,M.; Fasoli,E.; Fiorini,M.; Prelli,F.; Frangione,B.; Tridente,G.; Bentivoglio,M.; Giorgi,A.; Schinina,M.E.; Maras,B.; Agrimi,U.; Rizzuto,N.; Pocchiari,M.; Monaco,S. - Novel prion protein conformation and glycotype in Creutzfeldt-Jakob disease - Archives of Neurology 2007 Apr; 64(4): 595-9
AWRA - Zanusso,G.; Polo,A.; Farinazzo,A.; Nonno,R.; Cardone,F.; Di Bari,M.; Ferrari,S.; Principe,S.; Gelati,M.; Fasoli,E.; Fiorini,M.; Prelli,F.; Frangione,B.; Tridente,G.; Bentivoglio,M.; Giorgi,A.; Schinina,M.E.; Maras,B.; Agrimi,U.; Pocchiari,M.; Rizzuto,N.; Monaco,S. - Novel prion protein conformation and glycotype in atypical Creutzfeldt Jakob Disease - International Conference - Prion 2006: Strategies, advances and trends towards protection of society - 3.10.-6.10.2006, Torino, Italy, Lingotto Conference Centre - Oral sessions ORAL-17
ARBG - Zanusso,G.; Farinazzo,A.; Prelli,F.; Fiorini,M.; Gelati,M.; Ferrari,S.; Righetti,P.G.; Rizzuto,N.; Frangione,B.; Monaco,S. - Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes - The Journal of Biological Chemistry 2004 Sep 10; 279(37): 38936-42
APAT - Zanusso,G.; Farinazzo,A.; Fiorini,M.; Ferrari,S.; Prelli,F.; Tagliavini,F.; Rizzuto,N.; Frangione,B.; Monaco,S. - Novel Proteinase K-Resistant Prion Protein Fragments Correlate to Sporadic Creutzfeldt-Jakob-Disease with Different Alleles - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - DG-61