Sfoglia per Autore
INHERITED PRION DISEASES
2004 Kong Q; Surewicz WK; Petersen RB; Zou W; Chen SG; Gambetti P; Parchi P; Capellari S; Goldfarb L; Montagna P; Lugaresi E; Piccardo P; Ghetti B.
Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease
2004 Castellani R.J.; Colucci M.; Xie Z.; Zou W.; Li C.; Parchi P.; Capellari S.; Pastore M.; Rahbar M.H.; Chen S.G.; Gambetti P.
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.
An in vivo proton magnetic resonance spectroscopy study of thalamus in prion disease
2005 R. Lodi; P. Parchi; C. Tonon; D. N. Manners; S. Capellari; A. Filla; E. Malucelli; G. Pierangeli; P. Cortelli; P. Montagna; B. Barbiroli
Prion disease: an in vivo proton magnetic resonance spectroscopy study of thalamus.
2005 C. Tonon; P. Parchi; R. Lodi; D. N. Manners; S. Capellari; A. Filla; E. Malucelli; G. Pierangeli; P. Cortelli; P. Montagna; B. Barbiroli
Variations at the Calpain 1 gene locus in sporadic Creutzfeldt-Jakob disease
2005 M. Cescatti; S. Capellari; P. Gambetti; P. Parchi
Diffusion-weighted MRI shows abnormalities in white and deep grey matter of prion patients.
2005 D.N. Manners; R. Lodi; P. Parchi; C. Tonon; S. Capellari; A. Filla; G. Pierangeli; C. Testa; P. Cortelli; P. Montagna; B. Barbiroli
Fragile X premutation tremor/ataxia syndrome (FXTAS): a case with characteristic clinical and MR features.
2005 Rizzo G.; Pizza F.; Scaglione C.; Tommasoni E.; Capellari S.; Ambrosetto P.; Martinelli P.
Reduced in Vivo thalamic N-Acetyl-Aspartate is a Diagnostic Marker of Prion Disease
2005 Lodi R.; Parchi P.; Tonon C.; Manners D.; Capellari S.; Filla A.; Malucelli E.; Pierangeli G.; Cortelli P.; Montagna P.; Barbiroli B.
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
Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding
2005 Zaidi SI; Richardson SL; Capellari S; Song L; Smith MA; Ghetti B; Sy MS; Gambetti P; Petersen RB
Abnormal ADC in the brain of prion disease patients: variation between brain structures.
2005 D. N. Manners; R. Lodi; P. Parchi; C. Tonon; S. Capellari; A. Filla; G. Pierangeli; C. Testa; P. Cortelli; P. Montagna; B. Barbiroli
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
History and state of the art of PrP-res “typing” in Creutzfeldt-Jakob disease
2005 P. Parchi; S. Notari; S. Strammiello; S. Capellari
Characterization of bovine and human cellular prion protein expressed in the central nervous system and in lymphoid organs
2005 V. Defaweux; R. Strammiello; S. Capellari; N. Antoine; C. Demonceau; G. Dorban; O. Jolois; E. Heinen; P. Parchi
Prion disease: diffusion-weighted mri shows abnormalities in white and deep grey matter
2005 C. Tonon; D.N. Manners; P. Parchi; R. Lodi; S. Capellari; A. Filla; G. Pierangeli; C. Testa; P. Cortelli; P. Montagna; B. Barbiroli.
Use of in vivo proton magnetic resonance spectroscopy in the differential diagnosis of prion diseases
2005 C. Tonon; P. Parchi; R. Lodi; D.N. Manners; S. Capellari; A. Filla; E. Malucelli; G. Pierangeli; P. Cortelli; P. Montagna; B. Barbiroli
Clinical and genetic study of an Italian family with Parkinsonism.
2005 Perillo G.; Capellari S.; Molinari M.; Guaraldi P.; Grimaldi D.; Nichelli P.; Cortelli P.
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
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
Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
---|---|---|---|---|---|---|
INHERITED PRION DISEASES | Kong Q; Surewicz WK; Petersen RB; Zou W; Chen SG; Gambetti P; Parchi P; Capellari S; Goldfarb L; ...Montagna P; Lugaresi E; Piccardo P; Ghetti B. | 2004-01-01 | - | Cold Spring Harbor Laboratory Press | 2.01 Capitolo / saggio in libro | - |
Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease | Castellani R.J.; Colucci M.; Xie Z.; Zou W.; Li C.; Parchi P.; Capellari S.; Pastore M.; Rahbar M....H.; Chen S.G.; Gambetti P. | 2004-01-01 | NEUROLOGY | - | 1.01 Articolo in rivista | - |
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 | - |
An in vivo proton magnetic resonance spectroscopy study of thalamus in prion disease | R. Lodi; P. Parchi; C. Tonon; D. N. Manners; S. Capellari; A. Filla; E. Malucelli; G. Pierangeli;... P. Cortelli; P. Montagna; B. Barbiroli | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
Prion disease: an in vivo proton magnetic resonance spectroscopy study of thalamus. | C. Tonon; P. Parchi; R. Lodi; D. N. Manners; S. Capellari; A. Filla; E. Malucelli; G. Pierangeli;... P. Cortelli; P. Montagna; B. Barbiroli | 2005-01-01 | NEUROLOGICAL SCIENCES | - | 4.02 Riassunto (Abstract) | - |
Variations at the Calpain 1 gene locus in sporadic Creutzfeldt-Jakob disease | M. Cescatti; S. Capellari; P. Gambetti; P. Parchi | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
Diffusion-weighted MRI shows abnormalities in white and deep grey matter of prion patients. | D.N. Manners; R. Lodi; P. Parchi; C. Tonon; S. Capellari; A. Filla; G. Pierangeli; C. Testa; P. C...ortelli; P. Montagna; B. Barbiroli | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
Fragile X premutation tremor/ataxia syndrome (FXTAS): a case with characteristic clinical and MR features. | Rizzo G.; Pizza F.; Scaglione C.; Tommasoni E.; Capellari S.; Ambrosetto P.; Martinelli P. | 2005-01-01 | NEUROLOGY | - | 4.02 Riassunto (Abstract) | - |
Reduced in Vivo thalamic N-Acetyl-Aspartate is a Diagnostic Marker of Prion Disease | Lodi R.; Parchi P.; Tonon C.; Manners D.; Capellari S.; Filla A.; Malucelli E.; Pierangeli G.; Co...rtelli P.; Montagna P.; Barbiroli B. | 2005-01-01 | NEUROLOGY | - | 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 | - |
Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding | Zaidi SI; Richardson SL; Capellari S; Song L; Smith MA; Ghetti B; Sy MS; Gambetti P; Petersen RB | 2005-01-01 | JOURNAL OF ALZHEIMER'S DISEASE | - | 1.01 Articolo in rivista | - |
Abnormal ADC in the brain of prion disease patients: variation between brain structures. | D. N. Manners; R. Lodi; P. Parchi; C. Tonon; S. Capellari; A. Filla; G. Pierangeli; C. Testa; P. ...Cortelli; P. Montagna; B. Barbiroli | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
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) | - |
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 | - |
Characterization of bovine and human cellular prion protein expressed in the central nervous system and in lymphoid organs |
V. Defaweux; R. Strammiello; S. Capellari; N. Antoine; C. Demonceau; G. Dorban; O. Jolois; E. He...inen; P. Parchi |
2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
Prion disease: diffusion-weighted mri shows abnormalities in white and deep grey matter | C. Tonon; D.N. Manners; P. Parchi; R. Lodi; S. Capellari; A. Filla; G. Pierangeli; C. Testa; P. C...ortelli; P. Montagna; B. Barbiroli. | 2005-01-01 | NEUROLOGICAL SCIENCES | - | 4.02 Riassunto (Abstract) | - |
Use of in vivo proton magnetic resonance spectroscopy in the differential diagnosis of prion diseases | C. Tonon; P. Parchi; R. Lodi; D.N. Manners; S. Capellari; A. Filla; E. Malucelli; G. Pierangeli; ...P. Cortelli; P. Montagna; B. Barbiroli | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
Clinical and genetic study of an Italian family with Parkinsonism. | Perillo G.; Capellari S.; Molinari M.; Guaraldi P.; Grimaldi D.; Nichelli P.; Cortelli P. | 2005-01-01 | NEUROLOGICAL SCIENCES | - | 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) | - |
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) | - |
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