Sfoglia per Autore
Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD.
2004 NOTARI S; CAPELLARI S; GIESE A; WESTNER I; BARUZZI A.; GHETTI B; GAMBETTI P; KRETZSCHMAR HA; PARCHI P.
History and state of the art of PrP-res “typing” in Creutzfeldt-Jakob disease
2005 P. Parchi; S. Notari; S. Strammiello; S. Capellari
Quantitative mass spectrometry analysis of the PrPTSE allotypes present in the brain of a diseased individual carrying the R208H mutation.
2005 S. Principe; L. Dimiziani; S. Notari; Q.G. Liu; F. Cardone; A. De Pascalis; S. Capellari; P. Roepstorff; B. Maras; P. Parchi; M.E. Schininà; M. Pocchiari
Heterogeneity of truncated fragments distinct from PrP27-30 correlates with clinico-pathological subtypes of Creutzfeldt-Jakob disease
2005 S Notari; S Capellari; A Giese; J Grassi; B Ghetti; P Gambetti; HA Kretzschmar; P Parchi
Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene
2005 S. Capellari; F. Cardone; S. Notari; M. E. Schininà; B. Maras; D. Sità; A. Baruzzi; M. Pocchiari; P. Parchi
HUMAN PRPSC “TYPING” PITFALLS ASSOCIATED WITH THE USE OF TYPE 1 SELECTIVE ANTIBODIES COMBINED WITH RELATIVE INEFFICIENT HYDROLYSIS OF PRPSC BY PROTEINASE K
2006 S. Notari ; S. Capellari; J.P. Langeveld; A. Giese; P. Gambetti; H.A. Kretzschmar; P. Parchi
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
2007 Capellari S; Notari S; Cescatti M; Pegoraro E; Pantieri R; Michelucci R; Parchi P
Quantitative Mass Spectrometry Analysis of the Pathological PrP Allotypes Present in the Brain of gCJD Affected Individuals
2007 Principe S; Schininà ME; Maras B; Cosentino D; Liu Q; Notari S; Capellari S; Parchi P; Cardone F
Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion Consortium.
2009 Parchi P.; Notari S.; Weber P.; Schimmel H.; Budka H.; Ferrer I.; Haik S.; Hauw J.J.; Head M.W.; Ironside J.W.; Limido L.; Rodriguez A.; Strobel T.; Tagliavini F.; Kretzschmar H.A.
The role of PrP and other proteins in prion diseases
2009 S. Principe; F. Cardone; L. Di Francesco; A. Giorgi; G. Mignogna; M. Sbriccoli; R. Galeno; S. Notari; S. Capellari; P. Parchi; J. Rappsilber; B. Maras; M.E. Schininà; M. Pocchiari
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States.
2010 Notari S.; Moleres F.J.; Hunter S.B.; Belay E.D.; Schonberger L.B.; Cali I.; Parchi P.; Shieh W.J.; Brown P.; Zaki S.; Zou W.Q.; Gambetti P.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD. | NOTARI S; CAPELLARI S; GIESE A; WESTNER I; BARUZZI A.; GHETTI B; GAMBETTI P; KRETZSCHMAR HA; PARC...HI P. | 2004-01-01 | THE JOURNAL OF BIOLOGICAL CHEMISTRY | - | 1.01 Articolo in rivista | - |
| History and state of the art of PrP-res “typing” in Creutzfeldt-Jakob disease | P. Parchi; S. Notari; S. Strammiello; S. Capellari | 2005-01-01 | - | Springer-Verlag | 2.01 Capitolo / saggio in libro | - |
| Quantitative mass spectrometry analysis of the PrPTSE allotypes present in the brain of a diseased individual carrying the R208H mutation. |
S. Principe; L. Dimiziani; S. Notari; Q.G. Liu; F. Cardone; A. De Pascalis; S. Capellari; P. Roe...pstorff; B. Maras; P. Parchi; M.E. Schininà; M. Pocchiari |
2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Heterogeneity of truncated fragments distinct from PrP27-30 correlates with clinico-pathological subtypes of Creutzfeldt-Jakob disease | S Notari; S Capellari; A Giese; J Grassi; B Ghetti; P Gambetti; HA Kretzschmar; P Parchi | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene | S. Capellari; F. Cardone; S. Notari; M. E. Schininà; B. Maras; D. Sità; A. Baruzzi; M. Pocchiari;... P. Parchi | 2005-01-01 | NEUROLOGY | - | 1.01 Articolo in rivista | - |
| HUMAN PRPSC “TYPING” PITFALLS ASSOCIATED WITH THE USE OF TYPE 1 SELECTIVE ANTIBODIES COMBINED WITH RELATIVE INEFFICIENT HYDROLYSIS OF PRPSC BY PROTEINASE K | S. Notari ; S. Capellari; J.P. Langeveld; A. Giese; P. Gambetti; H.A. Kretzschmar; P. Parchi | 2006-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| 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 | Capellari S; Notari S; Cescatti M; Pegoraro E; Pantieri R; Michelucci R; Parchi P | 2007-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Quantitative Mass Spectrometry Analysis of the Pathological PrP Allotypes Present in the Brain of gCJD Affected Individuals | Principe S; Schininà ME; Maras B; Cosentino D; Liu Q; Notari S; Capellari S; Parchi P; Cardone F | 2007-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion Consortium. | Parchi P.; Notari S.; Weber P.; Schimmel H.; Budka H.; Ferrer I.; Haik S.; Hauw J.J.; Head M.W.; ...Ironside J.W.; Limido L.; Rodriguez A.; Strobel T.; Tagliavini F.; Kretzschmar H.A. | 2009-01-01 | BRAIN PATHOLOGY | - | 1.01 Articolo in rivista | - |
| The role of PrP and other proteins in prion diseases | S. Principe; F. Cardone; L. Di Francesco; A. Giorgi; G. Mignogna; M. Sbriccoli; R. Galeno; S. Not...ari; S. Capellari; P. Parchi; J. Rappsilber; B. Maras; M.E. Schininà; M. Pocchiari | 2009-01-01 | CLINICAL NEUROPATHOLOGY | - | 4.02 Riassunto (Abstract) | - |
| Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States. | Notari S.; Moleres F.J.; Hunter S.B.; Belay E.D.; Schonberger L.B.; Cali I.; Parchi P.; Shieh W.J....; Brown P.; Zaki S.; Zou W.Q.; Gambetti P. | 2010-01-01 | PLOS ONE | - | 1.01 Articolo in rivista | journal.pone.0008765.PDF |
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