PARCHI, PIERO
PARCHI, PIERO
DIPARTIMENTO DI MEDICINA SPECIALISTICA, DIAGNOSTICA E SPERIMENTALE
Docenti di ruolo di IIa fascia
4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration
2020-01-01 Saijo E.; Metrick M.A.; Koga S.; Parchi P.; Litvan I.; Spina S.; Boxer A.; Rojas J.C.; Galasko D.; Kraus A.; Rossi M.; Newell K.; Zanusso G.; Grinberg L.T.; Seeley W.W.; Ghetti B.; Dickson D.W.; Caughey B.
A case of fatal familial insomnia in Africa.
2009-01-01 Baldin E.; Capellari S.; Provini F.; Corrado P.; Liguori R.; Parchi P.; Montagna P.; Cortelli P.
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Straussler-Scheinker disease phenotype: comparison with similar cases from the literature.
2011-01-01 Jansen C.; Voet W.; Head M.W.; Parchi P.; Yull H.; Verrips A.; Wesseling P.; Meulstee J.; Baas F.; van Gool W.A.; Ironside J.W.; Rozemuller A.J.
A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule.
2007-01-01 Notari S.; Capellari S.; Langeveld J.; Giese A.; Strammiello R.; Gambetti P.; Kretzschmar H.A.; Parchi P.
A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.
2011-01-01 Jansen C.; Parchi P.; Capellari S.; Strammiello R.; Dopper E.G.; van Swieten J.C.; Kamphorst W.; Rozemuller A.J.
Abnormal ADC in the brain of prion disease patients: variation between brain structures.
2005-01-01 D. N. Manners; R. Lodi; P. Parchi; C. Tonon; S. Capellari; A. Filla; G. Pierangeli; C. Testa; P. Cortelli; P. Montagna; B. Barbiroli
ADC and Proton Spectroscopy Reflect Cellular Pathology in Patients with Creutzfeldt-Jakob Disease
2006-01-01 D. N. Manners; P. Parchi; R. Lodi; C. Tonon; C. Testa; S. Capellari; G. Pierangeli; P. Cortelli; P. Montagna; B. Barbiroli
Age at onset in genetic prion disease and the design of preventive clinical trials
2019-01-01 Minikel E.V.; Vallabh S.M.; Orseth M.C.; Brandel J.-P.; Haik S.; Laplanche J.-L.; Zerr I.; Parchi P.; Capellari S.; Safar J.; Kenny J.; Fong J.C.; Takada L.T.; Ponto C.; Hermann P.; Knipper T.; Stehmann C.; Kitamoto T.; Ae R.; Hamaguchi T.; Sanjo N.; Tsukamoto T.; Mizusawa H.; Collins S.J.; Chiesa R.; Roiter I.; de Pedro-Cuesta J.; Calero M.; Geschwind M.D.; Yamada M.; Nakamura Y.; Mead S.
Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by theCYP4X1gene
2018-01-01 Poleggi, Anna; van der Lee, Sven; Capellari, Sabina; Puopolo, Maria; Ladogana, Anna; De Pascali, Eleonora; Lia, Debora; Formato, Alessia; Bartoletti-Stella, Anna; Parchi, Piero; van Duijn, Cornelia; Pocchiari, Maurizio
Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.
2010-01-01 Parchi P.; Cescatti M.; Notari S.; Schulz-Schaeffer W.J.; Capellari S.; Giese A.; Zou W.Q.; Kretzschmar H.; Ghetti B.; Brown P.
Agrypnia Excitata
2008-01-01 Cirignotta F; Mondini S; La Morgia C; Rinaldi R; Parchi P; Lodi R.
"Agrypnia excitata'' in a case of sporadic Creutzfeldt-Jakob disease VV2
2009-01-01 La Morgia C.; Parchi P.; Capellari S.; Lodi R.; Tonon C.; Rinaldi R.; Mondini S.; Cirignotta F.
An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene.
2010-01-01 Masullo C; Bizzarro A; Guglielmi V; Iannaccone E; Minicuci G; Vita MG; Capellari S; Parchi P; Servidei S
An in vivo proton magnetic resonance spectroscopy study of thalamus in prion disease
2005-01-01 R. Lodi; P. Parchi; C. Tonon; D. N. Manners; S. Capellari; A. Filla; E. Malucelli; G. Pierangeli; P. Cortelli; P. Montagna; B. Barbiroli
An update of the epidemiology of sporadic Creutzfeldt-Jakob disease in Italy based on neuropathologic and molecular typing of a large cohort of patients
2009-01-01 G. Giaccone; S. Capellari; L. Ingrosso; S. Ferrari; D. Imperiale; S. Taraglio; S. Monaco; M. Pocchiari; F. Tagliavini; P. Parchi
Analyses of Protease Resistance and Aggregation State of Abnormal Prion Protein across the Spectrum of Human Prions
2013-01-01 D. Saverioni;S. Notari;S. Capellari;I. Poggiolini;A. Giese;H. A. Kretzschmar;P. Parchi
Analysis of Conformational Stability of Abnormal Prion Protein Aggregates across the Spectrum of Creutzfeldt-Jakob Disease Prions
2016-01-01 Cescatti, Maura; Saverioni, Daniela; Capellari, Sabina; Tagliavini, Fabrizio; Kitamoto, Tetsuyuki; Ironside, James; Giese, Armin; Parchi, Piero
Analysis of polymorphisms in PRNP 5' UTR region in sCJD subtypres
2008-01-01 Capellari S; Corrado P; Gambetti P; Parchi P
Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease
2019-01-01 Bartoletti-Stella A.; Corrado P.; Mometto N.; Baiardi S.; Durrenberger P.F.; Arzberger T.; Reynolds R.; Kretzschmar H.; Capellari S.; Parchi P.
Antemortem CSF Aβ42/Aβ40 ratio predicts Alzheimer's disease pathology better than Aβ42 in rapidly progressive dementias
2019-01-01 Baiardi S.; Abu-Rumeileh S.; Rossi M.; Zenesini C.; Bartoletti-Stella A.; Polischi B.; Capellari S.; Parchi P.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration | Saijo E.; Metrick M.A.; Koga S.; Parchi P.; Litvan I.; Spina S.; Boxer A.; Rojas J.C.; Galasko D.; Kraus A.; Rossi M.; Newell K.; Zanusso G.; Grinberg L.T.; Seeley W.W.; Ghetti B.; Dickson D.W.; Caughey B. | 2020-01-01 | ACTA NEUROPATHOLOGICA | - | 1.01 Articolo in rivista | - |
| A case of fatal familial insomnia in Africa. | Baldin E.; Capellari S.; Provini F.; Corrado P.; Liguori R.; Parchi P.; Montagna P.; Cortelli P. | 2009-01-01 | JOURNAL OF NEUROLOGY | - | 1.04 Replica / breve intervento (e simili) | - |
| A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Straussler-Scheinker disease phenotype: comparison with similar cases from the literature. | Jansen C.; Voet W.; Head M.W.; Parchi P.; Yull H.; Verrips A.; Wesseling P.; Meulstee J.; Baas F.; van Gool W.A.; Ironside J.W.; Rozemuller A.J. | 2011-01-01 | ACTA NEUROPATHOLOGICA | - | 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.; Parchi P. | 2007-01-01 | LABORATORY INVESTIGATION | - | 1.01 Articolo in rivista | - |
| A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient. | Jansen C.; Parchi P.; Capellari S.; Strammiello R.; Dopper E.G.; van Swieten J.C.; Kamphorst W.; Rozemuller A.J. | 2011-01-01 | JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY | - | 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) | - |
| 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) | - |
| Age at onset in genetic prion disease and the design of preventive clinical trials | Minikel E.V.; Vallabh S.M.; Orseth M.C.; Brandel J.-P.; Haik S.; Laplanche J.-L.; Zerr I.; Parchi P.; Capellari S.; Safar J.; Kenny J.; Fong J.C.; Takada L.T.; Ponto C.; Hermann P.; Knipper T.; Stehmann C.; Kitamoto T.; Ae R.; Hamaguchi T.; Sanjo N.; Tsukamoto T.; Mizusawa H.; Collins S.J.; Chiesa R.; Roiter I.; de Pedro-Cuesta J.; Calero M.; Geschwind M.D.; Yamada M.; Nakamura Y.; Mead S. | 2019-01-01 | NEUROLOGY | - | 1.01 Articolo in rivista | 401406.full.pdf |
| Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by theCYP4X1gene | Poleggi, Anna; van der Lee, Sven; Capellari, Sabina; Puopolo, Maria; Ladogana, Anna; De Pascali, Eleonora; Lia, Debora; Formato, Alessia; Bartoletti-Stella, Anna; Parchi, Piero; van Duijn, Cornelia; Pocchiari, Maurizio | 2018-01-01 | JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease. | Parchi P.; Cescatti M.; Notari S.; Schulz-Schaeffer W.J.; Capellari S.; Giese A.; Zou W.Q.; Kretzschmar H.; Ghetti B.; Brown P. | 2010-01-01 | BRAIN | - | 1.01 Articolo in rivista | - |
| Agrypnia Excitata | Cirignotta F; Mondini S; La Morgia C; Rinaldi R; Parchi P; Lodi R. | 2008-01-01 | SLEEP | - | 4.02 Riassunto (Abstract) | - |
| "Agrypnia excitata'' in a case of sporadic Creutzfeldt-Jakob disease VV2 | La Morgia C.; Parchi P.; Capellari S.; Lodi R.; Tonon C.; Rinaldi R.; Mondini S.; Cirignotta F. | 2009-01-01 | JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene. | Masullo C; Bizzarro A; Guglielmi V; Iannaccone E; Minicuci G; Vita MG; Capellari S; Parchi P; Servidei S | 2010-01-01 | NEUROLOGICAL SCIENCES | - | 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) | - |
| An update of the epidemiology of sporadic Creutzfeldt-Jakob disease in Italy based on neuropathologic and molecular typing of a large cohort of patients | G. Giaccone; S. Capellari; L. Ingrosso; S. Ferrari; D. Imperiale; S. Taraglio; S. Monaco; M. Pocchiari; F. Tagliavini; P. Parchi | 2009-01-01 | CLINICAL NEUROPATHOLOGY | - | 4.02 Riassunto (Abstract) | - |
| Analyses of Protease Resistance and Aggregation State of Abnormal Prion Protein across the Spectrum of Human Prions | D. Saverioni;S. Notari;S. Capellari;I. Poggiolini;A. Giese;H. A. Kretzschmar;P. Parchi | 2013-01-01 | THE JOURNAL OF BIOLOGICAL CHEMISTRY | - | 1.01 Articolo in rivista | - |
| Analysis of Conformational Stability of Abnormal Prion Protein Aggregates across the Spectrum of Creutzfeldt-Jakob Disease Prions | Cescatti, Maura; Saverioni, Daniela; Capellari, Sabina; Tagliavini, Fabrizio; Kitamoto, Tetsuyuki; Ironside, James; Giese, Armin; Parchi, Piero | 2016-01-01 | JOURNAL OF VIROLOGY | - | 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) | - |
| Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease | Bartoletti-Stella A.; Corrado P.; Mometto N.; Baiardi S.; Durrenberger P.F.; Arzberger T.; Reynolds R.; Kretzschmar H.; Capellari S.; Parchi P. | 2019-01-01 | MOLECULAR NEUROBIOLOGY | - | 1.01 Articolo in rivista | Bartoletti_et_al_.pdf |
| Antemortem CSF Aβ42/Aβ40 ratio predicts Alzheimer's disease pathology better than Aβ42 in rapidly progressive dementias | Baiardi S.; Abu-Rumeileh S.; Rossi M.; Zenesini C.; Bartoletti-Stella A.; Polischi B.; Capellari S.; Parchi P. | 2019-01-01 | ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY | - | 1.01 Articolo in rivista | Baiardi_et_al-2019-Annals_of_Clinical_and_Translational_Neurology.pdf |