AATL - Arnold,S.E.; Trojanowski,J.Q.; Parchi,P. - Protease resistant prion proteins are not present in sporadic "poor outcome" schizophrenia - Journal of Neurology, Neurosurgery and Psychiatry 1999 Jan; 66(1): 90-2
AAVU - Avoni,P.; Cortelli,P.; Montagna,P.; Tinuper,P.; Sforza,E.; Contin,M.; Parchi,P.; Pierangeli,G.; Maltoni,P.; Pavani,A.; et al. - Circadian hormonal rhythms in two new cases of fatal familial insomnia - Acta Neurologica 1991 Dec; 13(6): 574-6
AAWQ - Bahn,M.M.; Parchi,P. - Abnormal diffusion-weighted magnetic resonance images in Creutzfeldt-Jakob disease - Archives of Neurology 1999 May; 56(5): 577-83
ABCW - Beaudry,P.; Parchi,P.; Peoc'h,K.; Desbordes,P.; Dartigues,J.F.; Vital,A.; Vital,C.; Capellari,S.; Gambetti,P.; Delasnerie-Laupretre,N.; Mary,J.Y.; Laplanche,J.L. - A French cluster of Creutzfeldt-Jakob disease: a molecular analysis. - European Journal of Neurology 2002 Sep; 9(5): 457-62
ABEL - Belay,E.D.; Gambetti,P.; Schonberger,L.B.; Parchi,P.; Lyon,D.R.; Capellari,S.; McQuiston,J.H.; Bradley,K.; Dowdle,G.; Crutcher,J.M.; Nichols,C.R. - Creutzfeldt-Jakob disease in unusually young patients who consumed venison - Archives of Neurology 2001 Oct; 58(10): 1673-8
AXKC - Cali,I.; Parchi,P.; Langeveld,J.P.M.; Zou,W.Q.; Gambetti,P. - Coexistence of Both PrPsc Type 1 and 2 in sCJD: Does it Affect the Phenotype? - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Pathology and Pathogenesis P03.179
AVFI - Cali,I.; Castellani,R.J.; Yuan,J.; Al-Shekhlee,A.; Cohen,M.L.; Xiao,X.; Moleres,F.J.; Parchi,P.; Zou,W.Q.; Gambetti,P. - Classification of sporadic Creutzfeldt-Jakob disease revisited - Brain: A Journal of Neurology 2006 Sep; 129(9): 2266-77
AXKF - Capellari,S.; Notari,S.; Cescatti,M.; Pegoraro,E.; Pantieri,R.; Michelucci,R.; Parchi,P. - CJD Associated with the E200K Mutation with Valine at Codon 129 on the Mutated Allele and Methionine on the Wild Type Allele: Report of Two Cases - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Pathology and Pathogenesis P03.83
AWCW - Capellari,S.; Cortelli,P.; Avoni,P.; Casadei,G.P.; Baruzzi,A.; Lugaresi,E.; Pocchiari,M.; Gambetti,P.; Montagna,P.; Parchi,P. - Sporadic fatal insomnia in a fatal familial insomnia pedigree - International Conference - Prion 2006: Strategies, advances and trends towards protection of society - 3.10.-6.10.2006, Torino, Italy, Lingotto Conference Centre - Poster sessions GEN-07
ATZK - Capellari,S.; Cardone,F.; Notari,S.; Schinina,M.E.; Maras,B.; Sita,D.; Baruzzi,A.; Pocchiari,M.; Parchi,P. - Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene - Neurology 2005 Mar 8; 64(5): 905-7
ACEO - Capellari,S.; Parchi,P.; Wolff,B.D.; Campbell,J.; Atkinson,R.; Posey,D.M.; Petersen,R.B.; Gambetti,P. - Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein gene - Neurology 2002 Nov 26; 59(10): 1628-30
ATYL - Capellari,S.; Ladogana,A.; Volpi,G.; Ronocaro,F.; Sita,D.; Baruzzi,A.; Pocchiari,M.; Parchi,P. - First report of the R208H-129MM haplotype in the prion protein gene in a European subject with CJD - Abstract Book of the XXXII Congress of the Italian Neurological Society 2001 S109, published and exclusively distributed to the Congress participants
ACEP - Capellari,S.; Parchi,P.; Russo,C.M.; Sanford,J.; Sy,M.S.; Gambetti,P.; Petersen,R.B. - Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain. - American Journal of Pathology 2000 Aug; 157(2): 613-22
ACES - Capellari,S.; Vital,C.; Parchi,P.; Petersen,R.B.; Ferrer,X.; Jarnier,D.; Pegoraro,E.; Gambetti,P.; Julien,J. - Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family - Neurology 1997 Jul; 49(1): 133-41
APNO - Capellari,S.; Parchi,P.; Landis,D.D.; Julien,J.; Vital,C.; Dickson,D.D.; Richardson,S.L.; Petersen,R.B.; Gambetti,P. - Prion encephalopathy with octapeptide repeats insertion - a study of 3 families - Neurology 1997; 48(N3): 5035
AROI - Castellani,R.J.; Colucci,M.; Xie,Z.; Zou,W.Q.; Li,C.; Parchi,P.; Capellari,S.; Pastore,M.; Rahbar,M.H.; Chen,S.G.; Gambetti,P. - Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease - Neurology 2004 Aug 10; 63(3): 436-42
ACIB - Castellani,R.J.; Parchi,P.; Madoff,L.; Gambetti,P.; McKeever,P. - Biopsy diagnosis of Creutzfeldt-Jakob disease by western blot: a case report. - Human Pathology 1997 May; 28(5): 623-6
ACIA - Castellani,R.J.; Parchi,P.; Stahl,J.; Capellari,S.; Cohen,M.L.; Gambetti,P. - Early pathologic and biochemical changes in Creutzfeldt-Jakob disease: study of brain biopsies. - Neurology 1996 Jun; 46(6): 1690-3
APNS - Castellani,R.J.; Parchi,P.; Stahl,J.; Coben,M.; Gambetti,P. - Biopsy diagnosis of Creutzfeldt-Jakob-disease by immunoblot analysis - Journal of Neuropathology and Experimental Neurology 1995; 54(N3): 448
ATMX - Cescatti,M.; Capellari,S.; Gambetti,P.; Parchi,P. - Variations at the Calpain 1 gene locus in sporadic Creutzfeldt-Jakob disease - 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-23
ACNU - Chen,S.G.; Zou,W.Q.; Parchi,P.; Gambetti,P. - PrPsc typing by N-terminal sequencing and mass spectrometry - Archives of Virology. Supplementum 2000(16): 209-16
ACNV - Chen,S.G.; Parchi,P.; Brown,P.; Capellari,S.; Zou,W.Q.; Cochran,E.J.; Vnencak-Jones,C.L.; Julien,J.; Vital,C.; Mikol,J.; Lugaresi,E.; Autilio-Gambetti,L.; Gambetti,P. - Allelic origin of the abnormal prion protein isoform in familial prion diseases - Nature Medicine 1997 Sep; 3(9): 1009-15
APOM - Chen,S.G.; Parchi,P.; Brown,P.; Roos,R.P.; Vnencak-Jones,C.L.; Gambetti,P. - Fatal familial insomnia and familial Creutzfeldt-Jakob disease - abnormal prion protein (PrPres) encoded by the mutant allele - Journal of Neuropathology and Experimental Neurology 1996; 55(N5): 636 Nr. 124
ACNW - Chen,S.G.; Teplow,D.B.; Parchi,P.; Teller,J.K.; Gambetti,P.; Autilio-Gambetti,L. - Truncated forms of the human prion protein in normal brain and in prion diseases - The Journal of Biological Chemistry 1995 Aug 11; 270(32): 19173-80
ARGI - Chretien,F.; Le Pavec,G.; Vallat-Decouvelaere,A.V.; Delisle,M.B.; Uro-Coste,E.; Ironside,J.W.; Gambetti,P.; Parchi,P.; Creminon,C.; Dormont,D.; Mikol,J.; Gray,F.; Gras,G. - Expression of excitatory amino acid transporter-1 (EAAT-1) in brain macrophages and microglia of patients with prion diseases - Journal of Neuropathology and Experimental Neurology 2004 Oct; 63(10): 1058-71
ATZQ - Cortelli,P.; Perani,D.; Montagna,P.; Gallassi,R.; Tinuper,P.; Federica,P.; Avoni,P.; Ferrillo,F.; Anchisi,D.; Moresco,R.M.; Fazio,F.; Parchi,P.; Baruzzi,A.; Lugaresi,E.; Gambetti,P. - Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies. - Brain: A Journal of Neurology 2006 Mar; 129(3): 668-75
ACWT - Cortelli,P.; Perani,D.; Parchi,P.; Grassi,F.; Montagna,P.; De Martin,M.; Castellani,R.J.; Tinuper,P.; Gambetti,P.; Lugaresi,E.; Fazio,F. - Cerebral metabolism in fatal familial insomnia: relation to duration, neuropathology, and distribution of protease-resistant prion protein. - Neurology 1997 Jul; 49(1): 126-33
ACWU - Cortelli,P.; Parchi,P.; Contin,M.; Pierangeli,G.; Avoni,P.; Tinuper,P.; Montagna,P.; Baruzzi,A.; Gambetti,P.L.; Lugaresi,E. - Cardiovascular dysautonomia in fatal familial insomnia - Clinical Autonomic Research 1991 Mar; 1(1): 15-21
ACXZ - Creange,A.; Gray,F.; Cesaro,P.; Adle-Biassette,H.; Duvoux,C.; Cherqui,D.; Bell,J.; Parchi,P.; Gambetti,P.; Degos,J.D. - Creutzfeldt-Jakob disease after liver transplantation - Annals of Neurology 1995 Aug; 38(2): 269-72
APPM - Creange,A.; Gray,F.; Cesaro,P.; Bell,J.; Parchi,P.; Gambetti,P.; Degos,J.D. - Creutzfeldt-Jakob-disease after liver-transplant - Journal of Neuropathology and Experimental Neurology 1995; 54(N3): 449, Abstraktnummer 152
ATPM - Defaweux,V.; Strammiello,R.; Capellari,S.; Antoine,N.; Demonceau,C.; Dorban,G.; Jolois,O.; Heinen,E.; Parchi,P. - Characterization of bovine and human cellular prion protein expressed in the central nervous system and in lymphoid organs - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Poster Session: Pathogenesis PATH-23
ADNZ - Dorandeu,A.; Wingertsmann,L.; Chretien,F.; Delisle,M.B.; Vital,C.; Parchi,P.; Montagna,P.; Lugaresi,E.; Ironside,J.W.; Budka,H.; Gambetti,P.; Gray,F. - Neuronal apoptosis in fatal familial insomnia - Brain Pathology 1998 Jul; 8(3): 531-7
APHH - Gambetti,P.; Kong,Q.; Zou,W.Q.; Parchi,P.; Chen,S.G. - Sporadic and familial CJD: classification and characterisation. - British Medical Bulletin 2003; 66: 213-39
AOCS - Gambetti,P.; Parchi,P.; Chen,S.G. - Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia - Clinics in Laboratory Medicine 2003 Mar; 23(1): 43-64
AEJY - Gambetti,P.; Parchi,P.; Capellari,S.; Russo,C.; Tabaton,M.; Teller,J.K.; Chen,S.G. - Mechanisms of phenotypic heterogeneity in prion, Alzheimer and other conformational diseases - Journal of Alzheimer's Disease : JAD 2001 Feb; 3(1): 87-95
AEJZ - Gambetti,P.; Parchi,P. - Insomnia in prion diseases: sporadic and familial. - The New England Journal of Medicine 1999 May 27; 340(21): 1675-7
AEKE - Gambetti,P.; Parchi,P.; Petersen,R.B.; Chen,S.G.; Lugaresi,E. - Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features. - Brain Pathology 1995 Jan; 5(1): 43-51
AENB - Ghorayeb,I.; Series,C.; Parchi,P.; Sawan,B.; Guez,S.; Laplanche,J.L.; Capellari,S.; Gambetti,P.; Vital,C. - Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one case. - Neurology 1998 Jul; 51(1): 271-4
AFAL - Hainfellner,J.A.; Parchi,P.; Kitamoto,T.; Jarius,C.; Gambetti,P.; Budka,H. - A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein. - Annals of Neurology 1999 Jun; 45(6): 812-6
AFCA - Hannah,E.L.; Belay,E.D.; Gambetti,P.; Krause,G.; Parchi,P.; Capellari,S.; Hoffman,R.E.; Schonberger,L.B. - Creutzfeldt-Jakob disease after receipt of a previously unimplicated brand of dura mater graft - Neurology 2001 Apr 24; 56(8): 1080-3
ANRJ - Korth,C.; Kaneko,K.; Groth,D.; Heye,N.; Telling,G.; Mastrianni,J.A.; Parchi,P.; Gambetti,P.; Will,R.; Ironside,J.; Heinrich,C.; Tremblay,P.; DeArmond,S.J.; Prusiner,S.B. - Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene - Proceedings of the National Academy of Sciences of the United States of America 2003 Apr 15; 100(8): 4784-9
AXCD - Magherini,A.; Pentore,R.; Galassi,G.; Stucchi,C.M.; Capellari,S.; Parchi,P. - MV2 subtype of sporadic Creutzfeldt-Jakob disease presenting as corticobasal syndrome - Movement Disorders 2007 Apr 30; 22(6): 898-9
AXSR - Mellina,V.; Equestre,M.; Poleggi,A.; Ladogana,A.; Almonti,S.; Morocutti,A.; Bove,R.; Cupini,M.L.; Desiato,M.T.; De Simone,R.; Arciprete,F.; Paolucci,E.; Brusa,L.; Iani,C.; Capellari,S.; Parchi,P. - Creutzfeldt Jakob Disease Associated with the R208H-129V Haplotype in the Protein Gene - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Epidemiology, Risk Assessment and Transmission P04.108
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
AWLD - Notari,S.; Capellari,S.; Langeveld,J.P.M.; Giese,A.; Gambetti,P.; Kretzschmar,H.A.; Parchi,P. - Human PrPsc "typing" pitfalls associated with the use of type 1 selective antibodies combined with relative inefficient hydrolysis of PrPsc by proteinase K - 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-27
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
AJDM - Padovani,A.; D'Alessandro,M.; Parchi,P.; Cortelli,P.; Anzola,G.P.; Montagna,P.; Vignolo,L.A.; Petraroli,R.; Pocchiari,M.; Lugaresi,E.; Gambetti,P. - Fatal familial insomnia in a new Italian kindred - Neurology 1998 Nov; 51(5): 1491-4
ATGM - Parchi,P. - Molecular heterogeneity in human TSEs: PrP27-30 typing and beyond - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Oral sessions ORAL-43
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
AJES - Parchi,P.; Capellari,S.; Gambetti,P. - Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia - Microscopy Research and Technique 2000 Jul 1; 50(1): 16-25
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
AJEU - Parchi,P.; Capellari,S.; Chin,S.S.M.; Schwarz,H.B.; Schecter,N.P.; Butts,J.D.; Hudkins,P.; Burns,D.K.; Powers,J.M.; Gambetti,P. - A subtype of sporadic prion disease mimicking fatal familial insomnia - Neurology 1999 Jun 10; 52(9): 1757-63
AJEV - Parchi,P.; Petersen,R.B.; Chen,S.G.; Autilio-Gambetti,L.; Capellari,S.; Monari,L.; Cortelli,P.; Montagna,P.; Lugaresi,E.; Gambetti,P. - Molecular pathology of fatal familial insomnia - Brain Pathology 1998 Jul; 8(3): 539-48
AJEW - Parchi,P.; Chen,S.G.; Brown,P.; Zou,W.Q.; Capellari,S.; Budka,H.; Hainfellner,J.A.; Reyes,P.F.; Golden,G.T.; Hauw,J.J.; Gajdusek,D.C.; Gambetti,P. - Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease - Proceedings of the National Academy of Sciences of the United States of America 1998 Jul 7; 95(14): 8322-7
AJEX - Parchi,P.; Capellari,S.; Chen,S.G.; Petersen,R.B.; Gambetti,P.; Kopp,N.; Brown,P.; Kitamoto,T.; Tateishi,J.; Giese,A.; Kretzschmar,H.A. - Typing prion isoforms - Nature 1997 Mar 20; 386(6622): 232-4
ASDT - Parchi,P.; Capellari,S.; Brown,P.; Budka,H.; Hainfellner,J.A.; Duyckaerts,C.; Gambetti,P. - Proteinase-k (pk) resistant prion protein-fragments in the P102L variant of Gerstmann-Sträussler-Scheinker-disease - Neurology 1997; 48(N3): 5033
AQRR - Parchi,P.; Petersen,R.B.; Gambetti,P. - New topics in familial prion diseases - Seminars in Virology 1996; 7(N3): 181-7
AQRS - Parchi,P.; Capellari,S.; Sima,A.A.F.; D'Amato,C.; McKeever,P.; Mikol,J.; Brion,S.; Brown,P.; Chen,S.G.; Petersen,R.B.; Gambetti,P. - Creutzfeldt-Jakob-disease (CJD) with 178(Asn) mutation in the prion protein gene - neuropathological and molecular-features - Journal of Neuropathology and Experimental Neurology 1996; 55(N5): 635 Nr. 121
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
AJEZ - Parchi,P.; Gambetti,P. - Human prion diseases - Current Opinion in Neurology 1995 Aug; 8(4): 286-93
AJFA - Parchi,P.; Castellani,R.J.; Cortelli,P.; Montagna,P.; Chen,S.G.; Petersen,R.B.; Manetto,V.; Vnencak-Jones,C.L.; McLean,M.J.; Sheller,J.R.; Lugaresi,E.; Autilio-Gambetti,L.; Gambetti,P. - Regional distribution of protease-resistant prion protein in fatal familial insomnia - Annals of Neurology 1995 Jul; 38(1): 21-9
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
ASHL - Perani,D.; Parchi,P.; Cortelli,P.; Montagna,P.; Grassi,F.; Castellani,R.J.; Gambetti,P.; Lugaresi,E.; Fazio,F. - Relationship between protease-resistant prion protein distribution and in-vivo regional cerebral metabolism in fatal familial insomnia (FFI) - Neurology 1995; 45(4): A 406-406
AJKF - Petersen,R.B.; Parchi,P.; Richardson,S.L.; Urig,C.B.; Gambetti,P. - Effect of the D178N mutation and the codon 129 polymorphism on the metabolism of the prion protein - The Journal of Biological Chemistry 1996 May 24; 271(21): 12661-8
ASHM - Petersen,R.B.; Capellari,S.; Chen,S.G.; Parchi,P.; Singh,N.; Zanusso,G.; Gambetti,P. - Inherited prion disease - a model system for studying protein processing - Molecular Biology of the Cell 1996 Dec; 7(Supplement, Poster Sessions, Pt. II, 68a): 396
AXUV - Principe,S.; Schinina,M.E.; Maras,B.; Cosentino,D.; Liu,Q.G.; Notari,S.; Capellari,S.; Parchi,P.; Cardone,F. - Quantitative Mass Spectrometry Analysis of the Pathological PrP Allotypes Present in the Brain of gCJD Affected Individuals - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Protein Misfolding P01.15
ATPQ - Principe,S.; Dimiziani,L.; Notari,S.; Liu,Q.G.; Cardone,F.; De Pascalis,A.; Capellari,S.; Roepstorff,P.; Maras,B.; Parchi,P.; Schinina,M.E.; Pocchiari,M. - Quantitative mass spectrometry analysis of the PrPtse allotypes present in the brain of a diseased individual carrying the R208H mutation - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Poster Session: Pathogenesis PATH-27
AKWO - Sima,A.A.F.; Defendini,R.; Keohane,C.; D'Amato,C.; Foster,N.L.; Parchi,P.; Gambetti,P.; Lynch,T.; Wilhelmsen,K.C. - The neuropathology of chromosome 17-linked dementia - Annals of Neurology 1996 Jun; 39(6): 734-43
AWON - Strammiello,R.; Cescatti,M.; Farquhar,C.; Marshall,A.; Mai,J.; Beekes,M.; Parchi,P. - Physico-chemical properties of PrPres in peripheral tissues of experimental TSEs - 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-31
ATKP - Strammiello,R.; Parchi,P. - Effect of different extraction procedures on PrPres detection limits and PrPres "typing" in peripheral tissues - International Conference - Prion 2005: Between fundamentals and society's needs - 19.10.-21.10.2005, Congress Center Düsseldorf - Poster Session: Diagnosis DIA-27
ALPJ - Telling,G.C.; Parchi,P.; DeArmond,S.J.; Cortelli,P.; Montagna,P.; Gabizon,R.; Mastrianni,J.A.; Lugaresi,E.; Gambetti,P.; Prusiner,S.B. - Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity - Science 1996 Dec 20; 274(5295): 2079-82
AMBH - Vital,C.; Gray,F.; Vital,A.; Parchi,P.; Capellari,S.; Petersen,R.B.; Ferrer,X.; Jarnier,D.; Julien,J.; Gambetti,P. - Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits. - Neuropathology and Applied Neurobiology 1998 Apr; 24(2): 125-30
ARXB - Vital,C.; Gray,F.; Vital,A.; Parchi,P.; Capellari,S.; Petersen,R.B.; Julien,J.; Gambetti,P. - Cerebellar modifications at immunohistochemical study (IHC) in 3 cases of prion encephalopathy with octapeptide repeat insertion (OPRI) - Journal of Neuropathology and Experimental Neurology 1997; 56(N5): 591 Nr. 79
AMSW - Worrall,B.B.; Herman,S.T.; Capellari,S.; Lynch,T.; Chin,S.S.M.; Gambetti,P.; Parchi,P. - Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease - Journal of Neurology, Neurosurgery and Psychiatry 1999 Nov; 67(5): 671-4
APNK - Zou,W.Q.; Capellari,S.; Parchi,P.; Sy,M.S.; Gambetti,P.; Chen,S.G. - Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease - The Journal of Biological Chemistry 2003 Oct 17; 278(42): 40429-36