Sfoglia per Autore
ADC and Proton Spectroscopy Reflect Cellular Pathology in Patients with Creutzfeldt-Jakob Disease
2006 D. N. Manners; P. Parchi; R. Lodi; C. Tonon; C. Testa; S. Capellari; G. Pierangeli; P. Cortelli; P. Montagna; B. Barbiroli
SPORADIC FATAL INSOMNIA IN A FATAL FAMILIAL INSOMNIA PEDIGREE
2006 S. Capellari; P. Cortelli; P. Avoni; G.P. Casadei; A. Baruzzi; E. Lugaresi; M. Pocchiari; P. Gambetti; P Montagna; 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
Task-specific dystonia as the onset of a neurodegenerative disease.
2007 Alessandria M; Rizzo G; Capellari S; Tugnoli V; Martinelli P; Montagna P; Cortelli P.
La risonanza magnetica di diffusione differenzia la degenerazione corticobasale dalla paralisi sopranucleare progressiva e dalla malattia di Parkinson.
2007 Rizzo G; Manners DN; Scaglione C; Tonon C; Mostacci B; Cortelli P; Capellari S; Parchi P; Malucelli E; Barbiroli B; Lodi R; Martinelli P.
Diffusion-weighted imaging differentiates corticobasal degeneration from progressive supranuclear palsy and Parkinson’s disease.
2007 Rizzo G; Manners DN; Scaglione C; Tonon C; Mostacci B; Cortelli P; Capellari S; Parchi P; Malucelli E; Barbiroli B; Lodi R; Martinelli P.
Creutzfeldt Jakob Disease Associated with the R208H-129V Haplotype in the Protein Gene
2007 Mellina V, Equestre M; Poleggi A; Ladogana A; Almonti S; Morocutti A; Bove R; Cupini ML; Desiato MT; De Simone R; Arciprete F; Paolucci E; Brusa L; Iani C; Capellari S; Parchi P
Effects of Formalin Fixation, Paraffin Embedding, and Time of Storage on DNA Preservation in Brain Tissue: A BrainNet Europe Study
2007 Isidre Ferrer; Judith Armstrong; Sabina Capellari; Piero Parchi; Thomas Arzberger; Jeanne Bell; Herbert Budka; Thomas Ströbel; Giorgio Giaccone; Giacomina Rossi; Nenad Bogdanovic; Peter Fakai; Andrea Schmitt; Peter Riederers; Safa Al-Sarraj; Rivka Ravid; Hans Kretzschmar
MV2 subtype of sporadic Creutzfeldt-Jakob disease presenting as corticobasal syndrome
2007 Anna Magherini; Roberta Pentore; Giuliana Galassi; Carlo M. Stucchi; Sabina Capellari; Piero Parchi
A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule.
2007 Notari S.; Capellari S.; Langeveld J.; Giese A.; Strammiello R.; Gambetti P.; Kretzschmar H.A.; Parchi P.
Analysis of polymorphisms in PRNP 5' UTR region in sCJD subtypres
2008 Capellari S; Corrado P; Gambetti P; Parchi P
Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease
2008 G G Kovacs; P Sanchez-Juan; T Strobel; M Schuur; A Poleggi; S Nocentini; C Giannattasio; G Belay; M Bishop; S Capellari; P Parchi; E Gelpi; A Gal; A Bakos; M J. Molnar; U Heinemann; I Zerr; Richar S.G. Knight; Eva Mitrova; Cornelia van Duijn; Herbert Budka
Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease.
2008 Notari S; Strammiello R; Capellari S; Giese A; Cescatti M; Grassi J; Ghetti B; Langeveld JP; Zou WQ; Gambetti P; Kretzschmar HA; Parchi P.
Diagnostic profiles of young patients referred to the CJD Italian surveillance units
2008 Ladogana A; Mellina V; Almonti S; Puopolo M; Poleggi A; Capellari S; Parchi P; Pocchiari M
Microglial activation in sporadic CJD: regional variability and the effect of disease subtype
2008 Strammiello R; Capellari S; Parchi P
Mixed Brain Pathologies in Dementia: The BrainNet Europe Consortium Experience.
2008 Kovacs GG; Alafuzoff I; Al-Sarraj S; Arzberger T; Bogdanovic N; Capellari S; Ferrer I; Gelpi E; Kövari V; Kretzschmar H; Nagy Z; Parchi P; Seilhean D; Soininen H; Troakes C; Budka H.
Sporadic fatal insomnia in a fatal familial insomnia pedigree.
2008 Capellari S.; Parchi P.; Cortelli P.; Avoni P.; Casadei G.P.; Bini C.; Baruzzi A.; Lugaresi E.; Pocchiari M.; Gambetti P.; Montagna P.
Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation
2008 A. B. Rodríguez-Martínez; M. A. Alfonso-Sánchez; J. A. Peña; R Sánchez-Valle; I. Zerr; S. Capellari; M. Calero; J. J. Zarranz and M. M. de Pancorbo
Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease.
2008 Rizzo G.; Martinelli P.; Manners D.; Scaglione C.; Tonon C.; Cortelli P.; Malucelli E.; Capellari S.; Testa C.; Parchi P.; Montagna P.; Barbiroli B.; Lodi R.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| ADC and Proton Spectroscopy Reflect Cellular Pathology in Patients with Creutzfeldt-Jakob Disease | D. N. Manners; P. Parchi; R. Lodi; C. Tonon; C. Testa; S. Capellari; G. Pierangeli; P. Cortelli; ...P. Montagna; B. Barbiroli | 2006-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| SPORADIC FATAL INSOMNIA IN A FATAL FAMILIAL INSOMNIA PEDIGREE | S. Capellari; P. Cortelli; P. Avoni; G.P. Casadei; A. Baruzzi; E. Lugaresi; M. Pocchiari; P. Gamb...etti; P Montagna; 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) | - |
| Task-specific dystonia as the onset of a neurodegenerative disease. | Alessandria M; Rizzo G; Capellari S; Tugnoli V; Martinelli P; Montagna P; Cortelli P. | 2007-01-01 | NEUROLOGICAL SCIENCES | - | 4.02 Riassunto (Abstract) | - |
| La risonanza magnetica di diffusione differenzia la degenerazione corticobasale dalla paralisi sopranucleare progressiva e dalla malattia di Parkinson. | Rizzo G; Manners DN; Scaglione C; Tonon C; Mostacci B; Cortelli P; Capellari S; Parchi P; Malucel...li E; Barbiroli B; Lodi R; Martinelli P. | 2007-01-01 | - | LIMPE | 4.02 Riassunto (Abstract) | - |
| Diffusion-weighted imaging differentiates corticobasal degeneration from progressive supranuclear palsy and Parkinson’s disease. | Rizzo G; Manners DN; Scaglione C; Tonon C; Mostacci B; Cortelli P; Capellari S; Parchi P; Malucel...li E; Barbiroli B; Lodi R; Martinelli P. | 2007-01-01 | NEUROLOGICAL SCIENCES | - | 4.02 Riassunto (Abstract) | - |
| Creutzfeldt Jakob Disease Associated with the R208H-129V Haplotype in the Protein Gene | Mellina V, Equestre M; Poleggi A; Ladogana A; Almonti S; Morocutti A; Bove R; Cupini ML; Desiato ...MT; De Simone R; Arciprete F; Paolucci E; Brusa L; Iani C; Capellari S; Parchi P | 2007-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Effects of Formalin Fixation, Paraffin Embedding, and Time of Storage on DNA Preservation in Brain Tissue: A BrainNet Europe Study | Isidre Ferrer; Judith Armstrong; Sabina Capellari; Piero Parchi; Thomas Arzberger; Jeanne Bell; H...erbert Budka; Thomas Ströbel; Giorgio Giaccone; Giacomina Rossi; Nenad Bogdanovic; Peter Fakai; Andrea Schmitt; Peter Riederers; Safa Al-Sarraj; Rivka Ravid; Hans Kretzschmar | 2007-01-01 | BRAIN PATHOLOGY | - | 1.01 Articolo in rivista | - |
| MV2 subtype of sporadic Creutzfeldt-Jakob disease presenting as corticobasal syndrome | Anna Magherini; Roberta Pentore; Giuliana Galassi; Carlo M. Stucchi; Sabina Capellari; Piero Parchi | 2007-01-01 | MOVEMENT DISORDERS | - | 1.01 Articolo in rivista | - |
| A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule. | Notari S.; Capellari S.; Langeveld J.; Giese A.; Strammiello R.; Gambetti P.; Kretzschmar H.A.; P...archi P. | 2007-01-01 | LABORATORY INVESTIGATION | - | 1.01 Articolo in rivista | - |
| Analysis of polymorphisms in PRNP 5' UTR region in sCJD subtypres | Capellari S; Corrado P; Gambetti P; Parchi P | 2008-01-01 | - | sn | 4.02 Riassunto (Abstract) | - |
| Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease | G G Kovacs; P Sanchez-Juan; T Strobel; M Schuur; A Poleggi; S Nocentini; C Giannattasio; G Belay;... M Bishop; S Capellari; P Parchi; E Gelpi; A Gal; A Bakos; M J. Molnar; U Heinemann; I Zerr; Richar S.G. Knight; Eva Mitrova; Cornelia van Duijn; Herbert Budka | 2008-01-01 | - | sn | 4.02 Riassunto (Abstract) | - |
| Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease. | Notari S; Strammiello R; Capellari S; Giese A; Cescatti M; Grassi J; Ghetti B; Langeveld JP; Zou ...WQ; Gambetti P; Kretzschmar HA; Parchi P. | 2008-01-01 | THE JOURNAL OF BIOLOGICAL CHEMISTRY | - | 1.01 Articolo in rivista | - |
| Diagnostic profiles of young patients referred to the CJD Italian surveillance units | Ladogana A; Mellina V; Almonti S; Puopolo M; Poleggi A; Capellari S; Parchi P; Pocchiari M | 2008-01-01 | - | sn | 4.02 Riassunto (Abstract) | - |
| Microglial activation in sporadic CJD: regional variability and the effect of disease subtype | Strammiello R; Capellari S; Parchi P | 2008-01-01 | - | sn | 4.02 Riassunto (Abstract) | - |
| Mixed Brain Pathologies in Dementia: The BrainNet Europe Consortium Experience. |
Kovacs GG; Alafuzoff I; Al-Sarraj S; Arzberger T; Bogdanovic N; Capellari S; Ferrer I; Gelpi E; ...Kövari V; Kretzschmar H; Nagy Z; Parchi P; Seilhean D; Soininen H; Troakes C; Budka H. |
2008-01-01 | DEMENTIA AND GERIATRIC COGNITIVE DISORDERS | - | 1.01 Articolo in rivista | - |
| Sporadic fatal insomnia in a fatal familial insomnia pedigree. | Capellari S.; Parchi P.; Cortelli P.; Avoni P.; Casadei G.P.; Bini C.; Baruzzi A.; Lugaresi E.; P...occhiari M.; Gambetti P.; Montagna P. | 2008-01-01 | NEUROLOGY | - | 1.01 Articolo in rivista | - |
| Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation | A. B. Rodríguez-Martínez; M. A. Alfonso-Sánchez; J. A. Peña; R Sánchez-Valle; I. Zerr; S. Capella...ri; M. Calero; J. J. Zarranz and M. M. de Pancorbo | 2008-01-01 | NEUROGENETICS | - | 1.01 Articolo in rivista | - |
| Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease. | Rizzo G.; Martinelli P.; Manners D.; Scaglione C.; Tonon C.; Cortelli P.; Malucelli E.; Capellari... S.; Testa C.; Parchi P.; Montagna P.; Barbiroli B.; Lodi R. | 2008-01-01 | BRAIN | - | 1.01 Articolo in rivista | - |
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