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
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
ACEQ - Capellari,S.; Zaidi,S.I.A.; Long,A.C.; Kwon,E.E.; Petersen,R.B. - The Thr183Ala Mutation, Not the Loss of the First Glycosylation Site, Alters the Physical Properties of the Prion Protein - Journal of Alzheimer's Disease : JAD 2000 Mar; 2(1): 27-35
ACER - Capellari,S.; Zaidi,S.I.A.; Urig,C.B.; Perry,G.; Smith,M.A.; Petersen,R.B. - Prion protein glycosylation is sensitive to redox change - The Journal of Biological Chemistry 1999 Dec 3; 274(49): 34846-50
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
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
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
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
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
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
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
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
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
AIAK - Mastrianni,J.A.; Capellari,S.; Telling,G.C.; Han,D.; Bosque,P.J.; Prusiner,S.B.; DeArmond,S.J. - Inherited prion disease caused by the V210I mutation: transmission to transgenic mice. - Neurology 2001 Dec 26; 57(12): 2198-205
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
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
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
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
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
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
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
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
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
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