AAVG - Atzori,C.; Ghetti,B.; Piva,R.; Srinivasan,A.N.; Zolo,P.; Delisle,M.B.; Mirra,S.S.; Migheli,A. - Activation of the JNK/p38 pathway occurs in diseases characterized by tau protein pathology and is related to tau phosphorylation but not to apoptosis - Journal of Neuropathology and Experimental Neurology 2001 Dec; 60(12): 1190-7
AAWF - Azzarelli,B.; Muller,J.; Ghetti,B.; Dyken,M.; Conneally,P.M. - Cerebellar plaques in familial Alzheimer's disease (Gerstmann-Sträussler-Scheinker variant?) - Acta Neuropathologica 1985; 65(3-4): 235-46
AQXP - Barmada,S.J.; Piccardo,P.; Yamaguchi,K.; Ghetti,B.; Harris,D.A. - GFP-tagged prion protein is correctly localized and functionally active in the brains of transgenic mice - Neurobiology of Disease 2004 Aug; 16(3): 527-37
ABUP - Brown,P.; Cervenakova,L.; McShane,L.; Goldfarb,L.G.; Bishop,K.; Bastian,F.O.; Kirkpatrick,J.; Piccardo,P.; Ghetti,B.; Gajdusek,D.C. - Creutzfeldt-Jakob disease in a husband and wife - Neurology 1998 Mar; 50(3): 684-8
ABZY - Bugiani,O.; Giaccone,G.; Piccardo,P.; Morbin,M.; Tagliavini,F.; Ghetti,B. - Neuropathology of Gerstmann-Sträussler-Scheinker disease - Microscopy Research and Technique 2000 Jul 1; 50(1): 10-5
ACAA - Bugiani,O.; Giaccone,G.; Verga,L.; Pollo,B.; Frangione,B.; Farlow,M.R.; Tagliavini,F.; Ghetti,B. - Beta PP participates in PrP-amyloid plaques of Gerstmann-Sträussler-Scheinker disease, Indiana kindred - Journal of Neuropathology and Experimental Neurology 1993 Jan; 52(1): 64-70
ARON - Chiesa,R.; Piccardo,P.; Dossena,S.; Nowoslawski,L.; Roth,K.A.; Ghetti,B.; Harris,D.A. - Bax deletion prevents neuronal loss but not neurological symptoms in a transgenic model of inherited prion disease - Proceedings of the National Academy of Sciences of the United States of America 2005 Jan 4; 102(1): 238-43
ANXG - Chiesa,R.; Piccardo,P.; Quaglio,E.; Drisaldi,B.; Si-Hoe,S.L.; Takao,M.; Ghetti,B.; Harris,D.A. - Molecular Distinction between Pathogenic and Infectious Properties of the Prion Protein - Journal of Virology 2003 Jul 1; 77(13): 7611-7622
ACOT - Chiesa,R.; Pestronk,A.; Schmidt,R.E.; Tourtellotte,W.G.; Ghetti,B.; Piccardo,P.; Harris,D.A. - Primary myopathy and accumulation of PrPsc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation - Neurobiology of Disease 2001 Apr; 8(2): 279-88
ACOV - Chiesa,R.; Drisaldi,B.; Quaglio,E.; Migheli,A.; Piccardo,P.; Ghetti,B.; Harris,D.A. - Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation - Proceedings of the National Academy of Sciences of the United States of America 2000 May 9; 97(10): 5574-9
ACOW - Chiesa,R.; Piccardo,P.; Ghetti,B.; Harris,D.A. - Neurological illness in transgenic mice expressing a prion protein with an insertional mutation - Neuron 1998 Dec; 21(6): 1339-51
AUZA - Colucci,M.; Moleres,F.J.; Xie,Z.L.; Ray-Chaudhury,A.; Gutti,S.; Butefisch,C.M.; Cervenakova,L.; Wang,W.; Goldfarb,L.G.; Kong,Q.; Ghetti,B.; Chen,S.G.; Gambetti,P. - Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits. - Journal of Neuropathology and Experimental Neurology 2006 Jul; 65(7): 642-51
AOJS - de Michele,G.; Pocchiari,M.; Petraroli,R.; Manfredi,M.; Caneve,G.; Coppola,G.; Casali,C.; Sacca,F.; Piccardo,P.; Salvatore,E.; Berardelli,A.; Orio,M.; Barbieri,F.; Ghetti,B.; Filla,A. - Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family - Canadian Journal of Neurological Sciences 2003 Aug; 30(3): 233-6
AVWB - Di Fede,G.; Giaccone,G.; Limido,L.; Mangieri,M.; Suardi,S.; Puoti,G.; Morbin,M.; Mazzoleni,G.; Ghetti,B.; Tagliavini,F. - The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease - Journal of Neuropathology and Experimental Neurology 2007 Feb; 66(2): 124-30
ADLS - Dlouhy,S.R.; Hsiao,K.; Farlow,M.R.; Foroud,T.; Conneally,P.M.; Johnson,P.; Prusiner,S.B.; Hodes,M.E.; Ghetti,B. - Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene - Nature Genetics 1992 Apr; 1(1): 64-7
AWER - Farinazzo,A.; Zanusso,G.; Piccardo,P.; Ferrari,S.; Fasoli,E.; Gelati,M.; Fiorini,M.; Rizzuto,N.; Monaco,S.; Ghetti,B. - Two-dimensional analysis of proteinase K-resistant prion protein in GSS P102L mutation - International Conference - Prion 2006: Strategies, advances and trends towards protection of society - 3.10.-6.10.2006, Torino, Italy, Lingotto Conference Centre - Poster sessions PR-12
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
ADWE - Farlow,M.; Ghetti,B.; Dlouhy,S.; Giaccone,G.; Bugiani,O.; Tagliavini,F.; Wagner,S. - Cerebrospinal fluid levels of amyloid beta-protein precursor are low in Gerstmann-Sträussler-Scheinker disease, Indiana kindred - Neurology 1994 Aug; 44(8): 1508-10
ADWF - Farlow,M.R.; Yee,R.D.; Dlouhy,S.R.; Conneally,P.M.; Azzarelli,B.; Ghetti,B. - Gerstmann-Sträussler-Scheinker disease. I. Extending the clinical spectrum. - Neurology 1989 Nov; 39(11): 1446-52
AWEU - Ferrari,S.; Fasoli,E.; Zanusso,G.; Gelati,M.; Ghetti,B.; Monaco,S. - Immunocytochemistry and immunoelectron microscopy of PrP amyloid plaques in human prion disorders - International Conference - Prion 2006: Strategies, advances and trends towards protection of society - 3.10.-6.10.2006, Torino, Italy, Lingotto Conference Centre - Poster sessions PA-15
AWFI - Ghetti,B. - Gerstmann-Sträussler-Scheinker Disease (GSS) and prion protein cerebral amyloid angiopathy (PrP-CAA) - 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-26
AWFJ - Ghetti,B.; Kepe,V.; Bresjanac,M.; Huang,S.; Small,G.W.; Satyamurthy,N.; Farlow,M.R.; Epperson,F.; Repovs,G.; Smid,L.M.; Popovic,M.; Petric,A.; Phelps,M.E.; Barrio,J.R. - Visualization of PrP-amyloid disease with (F-18)FDDNP in Gerstmann-Sträussler-Scheinker (GSS) - International Conference - Prion 2006: Strategies, advances and trends towards protection of society - 3.10.-6.10.2006, Torino, Italy, Lingotto Conference Centre - Poster sessions DIA-17
AOCR - Ghetti,B.; Tagliavini,F.; Takao,M.; Bugiani,O.; Piccardo,P. - Hereditary prion protein amyloidoses - Clinics in Laboratory Medicine 2003 Mar; 23(1): 65-85, viii
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
AQDW - Ghetti,B.; Piccardo,P.; Farlow,M.R.; Dlouhy,S.R.; Tagliavini,F.; Giaccone,G.; Bugiani,O. - Distribution of abnormally phosphorylated-tau in Gerstmann-Sträussler-Scheinker-disease with mutation at codon-198 of the prion protein gene - Neurology 1996; 46(N2): 2065
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
AEMW - Ghetti,B.; Dlouhy,S.R.; Giaccone,G.; Bugiani,O.; Frangione,B.; Farlow,M.R.; Tagliavini,F. - Gerstmann-Sträussler-Scheinker disease and the Indiana kindred - Brain Pathology 1995 Jan; 5(1): 61-75
AEMX - Ghetti,B.; Tagliavini,F.; Giaccone,G.; Bugiani,O.; Frangione,B.; Farlow,M.R.; Dlouhy,S.R. - Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles - Molecular Neurobiology 1994 Feb; 8(1): 41-8
AEMY - Ghetti,B.; Tagliavini,F.; Masters,C.L.; Beyreuther,K.; Giaccone,G.; Verga,L.; Farlow,M.R.; Conneally,P.M.; Dlouhy,S.R.; Azzarelli,B.; et al. - Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family. - Neurology 1989 Nov; 39(11): 1453-61
AQAT - Giaccone,G.; Canciani,B.; Piccardo,P.; Tagliavini,F.; Ghetti,B.; Bugiani,O. - Topography of AT8 immunoreactivity in Gerstmann-Sträussler-Scheinker-disease, indiana kindred - Journal of Neuropathology and Experimental Neurology 1997; 56(N5): 588 Nr. 69
AENE - Giaccone,G.; Verga,L.; Bugiani,O.; Frangione,B.; Serban,D.; Prusiner,S.B.; Farlow,M.R.; Ghetti,B.; Tagliavini,F. - Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred - Proceedings of the National Academy of Sciences of the United States of America 1992 Oct 1; 89(19): 9349-53
AENF - Giaccone,G.; Tagliavini,F.; Verga,L.; Frangione,B.; Farlow,M.R.; Bugiani,O.; Ghetti,B. - Neurofibrillary tangles of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease share antigenic determinants with those of Alzheimer disease - Brain Research 1990 Oct 22; 530(2): 325-9
AOCL - Harris,D.A.; Chiesa,R.; Drisaldi,B.; Quaglio,E.; Migheli,A.; Piccardo,P.; Ghetti,B. - A murine model of a familial prion disease - Clinics in Laboratory Medicine 2003 Mar; 23(1): 175-86
AFDR - Harris,D.A.; Chiesa,R.; Drisaldi,B.; Quaglio,E.; Migheli,A.; Piccardo,P.; Ghetti,B. - A transgenic model of a familial prion disease - Archives of Virology. Supplementum 2000(16): 103-12
AFQC - Hsiao,K.K.; Dlouhy,S.R.; Farlow,M.R.; Cass,C.; Da Costa,M.M.; Conneally,P.M.; Hodes,M.E.; Ghetti,B.; Prusiner,S.B. - Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles - Nature Genetics 1992 Apr; 1(1): 68-71
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
AXRM - Limido,L.; Mangieri,M.; Capobianco,R.; Moda,F.; Vimercati,C.; Campagnani,I.; Catania,M.; Ghetti,B.; Giaccone,G.; Levy,E.; Tagliavini,F. - Role of Cystatin C in Prion Propagation and Prion Disease Pathogenesis - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Pathology and Pathogenesis P03.90
AQGJ - Mirra,S.S.; Gearing,M.; Jones,R.; Evatt,M.L.; Young,K.; Piccardo,P.; Ghetti,B. - Prion protein (PrP) amyloid coexists with neurofibrillary tangles and lewy bodies in a patient from a new family of Gerstmann-Sträussler-Scheinker disease (GSS) - Journal of Neuropathology and Experimental Neurology 1997; 56(N5): 596 Nr. 102
AQGK - Mirra,S.S.; Young,K.; Gearing,M.; Jones,R.; Evatt,M.L.; Piccardo,P.; Ghetti,B. - Coexistence of prion protein (PrP) amyloid, neurofibrillary tangles, and lewy bodies in Gerstmann-Sträussler-Scheinker- disease with prion gene (prnp) mutation F198S - Brain Pathology 1997; 7(N4): 1379
AIND - Monari,L.; Chen,S.G.; Brown,P.; Parchi,P.; Petersen,R.B.; Mikol,J.; Gray,F.; Cortelli,P.; Montagna,P.; Ghetti,B.; Goldfarb,L.G.; Gajdusek,D.C.; Lugaresi,E.; Gambetti,P.; Autilio-Gambetti,L. - Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. - Proceedings of the National Academy of Sciences of the United States of America 1994 Mar 29; 91(7): 2839-42
AVLJ - Moroncini,G.; Mangieri,M.; Morbin,M.; Mazzoleni,G.; Ghetti,B.; Gabrielli,A.; Williamson,R.A.; Giaccone,G.; Tagliavini,F. - Pathologic prion protein is specifically recognized in situ by a novel PrP conformational antibody - Neurobiology of Disease 2006 Sep; 23(3): 717-24
ATOD - Notari,S.; Capellari,S.; Giese,A.; Grassi,J.; Ghetti,B.; Gambetti,P.; Kretzschmar,H.A.; Parchi,P. - Heterogeneity of truncated fragments distinct from PrP27-30 correlates with clinico-pathological subtypes of Creutzfeldt-Jakob disease - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Poster Session: Human prions, risk of blood products, and therapy HUMAN-27
AQNG - Notari,S.; Capellari,S.; Giese,A.; Westner,I.; Baruzzi,A.; Ghetti,B.; Gambetti,P.; Kretzschmar,H.A.; Parchi,P. - Effects of different experimental conditions on the PrPsc core generated by protease digestion: implications for strain typing and molecular classification of CJD. - The Journal of Biological Chemistry 2004 Apr 16; 279(16): 16797-804
AOXM - Notari,S.; Capellari,S.; Giese,A.; Westner,I.; Ghetti,B.; Gambetti,P.; Kretzschmar,H.A.; Parchi,P. - Effects of different experimental conditions on the PrPsc core generated by protease digestion: Implications for strain typing and molecular classification of CJD - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - DG-75
AJEL - Panegyres,P.K.; Toufexis,K.; Kakulas,B.A.; Cervenakova,L.; Brown,P.; Ghetti,B.; Piccardo,P.; Dlouhy,S.R. - A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker disease - Archives of Neurology 2001 Nov; 58(11): 1899-902
AJER - Parchi,P.; Zou,W.Q.; Wang,W.; Brown,P.; Capellari,S.; Ghetti,B.; Kopp,N.; Schulz-Schaeffer,W.J.; Kretzschmar,H.A.; Head,M.W.; Ironside,J.W.; Gambetti,P.; Chen,S.G. - Genetic influence on the structural variations of the abnormal prion protein - Proceedings of the National Academy of Sciences of the United States of America 2000 Aug 29; 97(18): 10168-72
AJET - Parchi,P.; Giese,A.; Capellari,S.; Brown,P.; Schulz-Schaeffer,W.J.; Windl,O.; Zerr,I.; Budka,H.; Kopp,N.; Piccardo,P.; Poser,S.; Rojiani,A.; Streichenberger,N.; Julien,J.; Vital,C.; Ghetti,B.; Gambetti,P.; Kretzschmar,H.A. - Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects - Annals of Neurology 1999 Aug; 46(2): 224-33
AJEY - Parchi,P.; Castellani,R.J.; Capellari,S.; Ghetti,B.; Young,K.; Chen,S.G.; Farlow,M.; Dickson,D.W.; Sima,A.A.F.; Trojanowski,J.Q.; Petersen,R.B.; Gambetti,P. - Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease - Annals of Neurology 1996 Jun; 39(6): 767-78
ASDU - Parchi,P.; Castellani,R.J.; Capellari,S.; Petersen,R.B.; Chen,S.G.; Young,K.; Farlow,M.; Trojanowski,J.Q.; Sima,A.; Ghetti,B.; Gambetti,P. - Protease-resistant prion protein in sporadic Creutzfeldt-Jakob-disease (CJD) - correlation with clinicopathological features and PrP genotype - Journal of Neuropathology and Experimental Neurology 1995; 54(N3): 416
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
AXUL - Piccardo,P.; Manson,J.C.; King,D.; Ghetti,B.; Barron,R.M. - Murine Model of PrP-amyloid Formation without Spongiform Degeneration - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Pathology and Pathogenesis P03.67
AWVB - Piccardo,P.; Manson,J.C.; King,D.; Ghetti,B.; Barron,R.M. - Accumulation of prion protein in the brain that is not associated with transmissible disease - Proceedings of the National Academy of Sciences of the United States of America 2007 Mar 13; 104(11): 4712-7
AWLX - Piccardo,P.; King,D.; Ghetti,B.; Manson,J.C.; Barron,R.M. - Deposition of PrP amyloid in the absence of transmissible 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-39
AWLY - Piccardo,P.; King,D.; Campbell,S.; Ghetti,B.; Manson,J.C.; Barron,R.M. - Deposition of PrP amyloid in the absence of transmissible disease - International Conference - Prion 2006: Strategies, advances and trends towards protection of society - 3.10.-6.10.2006, Torino, Italy, Lingotto Conference Centre - Poster sessions PA-42
AJLA - Piccardo,P.; Liepnieks,J.J.; William,A.; Dlouhy,S.R.; Farlow,M.R.; Young,K.; Nochlin,D.; Bird,T.D.; Nixon,R.R.; Ball,M.J.; DeCarli,C.; Bugiani,O.; Tagliavini,F.; Benson,M.D.; Ghetti,B. - Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations - American Journal of Pathology 2001 Jun; 158(6): 2201-7
AJLB - Piccardo,P.; Dlouhy,S.R.; Lievens,P.M.J.; Young,K.; Bird,T.D.; Nochlin,D.; Dickson,D.W.; Vinters,H.V.; Zimmerman,T.R.Jr.; Mackenzie,I.R.; Kish,S.J.; Ang,L.C.; de Carli,C.; Pocchiari,M.; Brown,P.; Gibbs,C.J.Jr.; Gajdusek,D.C.; Bugiani,O.; Ironside,J.; Tagliavini,F.; Ghetti,B. - Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity - Journal of Neuropathology and Experimental Neurology 1998 Oct; 57(10): 979-88
AJLC - Piccardo,P.; Langeveld,J.P.M.; 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. - 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 bovine spongiform encephalopathy - American Journal of Pathology 1998 Jun; 152(6): 1415-20
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
AUDY - Stewart,R.S.; Piccardo,P.; Ghetti,B.; Harris,D.A. - Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein - Journal of Neuroscience 2005 Mar 30; 25(13): 3469-77
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
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
ALKO - Taratuto,A.L.; Piccardo,P.; Reich,E.G.; Chen,S.G.; Sevlever,G.; Schultz,M.; Luzzi,A.A.; Rugiero,M.; Abecasis,G.; Endelman,M.; Garcia,A.M.; Capellari,S.; Xie,Z.; Lugaresi,E.; Gambetti,P.; Dlouhy,S.R.; Ghetti,B. - Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease - Neurology 2002 Feb 12; 58(3): 362-7
ALVY - Unverzagt,F.W.; Farlow,M.R.; Norton,J.; Dlouhy,S.R.; Young,K.; Ghetti,B. - Neuropsychological function in patients with Gerstmann-Sträussler-Scheinker disease from the Indiana kindred (F198S) - Journal of the International Neuropsychological Society 1997 Mar; 3(2): 169-78
ASEX - Unverzagt,F.W.; Farlow,M.R.; Dlouhy,S.R.; Norton,J.; Mercado,N.; Torke,A.M.; Ghetti,B. - Presymptomatic neuropsychological deficits in gerstmann- Sträussler-scheinker disease - Annals of Neurology 1994; 36(N2): 272-3
AMVV - Yee,R.D.; Farlow,M.R.; Suzuki,D.A.; Betelak,K.F.; Ghetti,B. - Abnormal eye movements in Gerstmann-Sträussler-Scheinker disease - Archives of Ophthalmology 1992 Jan; 110(1): 68-74
ARYG - Young,K.; Russell,J.A.; Ma,J.M.; Hedleywhyte,T.E.; Dlouhy,S.R.; Piccardo,P.; Ghetti,B. - Gerstmann-Sträussler-Scheinker (GSS) disease with the prion protein gene (PrnP) P102L mutation and lower motor-neuron degeneration - Journal of Neuropathology and Experimental Neurology 1997; 56(N5): 596 Nr. 100
AMWU - Young,K.; Clark,H.B.; Piccardo,P.; Dlouhy,S.R.; Ghetti,B. - Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129 - Brain Research. Molecular Brain Research 1997 Feb; 44(1): 147-50
AMWV - Young,K.; Jones,C.K.; Piccardo,P.; Lazzarini,A.; Golbe,L.I.; Zimmerman,T.R.Jr.; Dickson,D.W.; Mclachlan,D.C.; St George-Hyslop,P.; Lennox,A.; Perlman,S.; Vinters,H.V.; Hodes,M.E.; Dlouhy,S.; Ghetti,B. - Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients - Neurology 1995 Jun; 45(6): 1127-34
ARYH - Young,K.; Piccardo,P.; Dlouhy,S.R.; Clark,H.B.; Ghetti,B. - Gerstmann-Sträussler-Scheinker (gss) disease with signal atrophy - Journal of Neuropathology and Experimental Neurology 1995; 54(N3): 448
ASUM - Zaidi,S.I.A.; Richardson,S.L.; Capellari,S.; Song,L.; Smith,M.A.; Ghetti,B.; Sy,M.S.; Gambetti,P.; Petersen,R.B. - Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding. - Journal of Alzheimer's Disease : JAD 2005 Apr; 7(2): 159-71; discussion 173-80