PARCHI, PIERO

PARCHI, PIERO  

DIPARTIMENTO DI MEDICINA SPECIALISTICA, DIAGNOSTICA E SPERIMENTALE  

Docenti di ruolo di IIa fascia  

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Risultati 1 - 20 di 207 (tempo di esecuzione: 0.035 secondi).
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.; P...archi 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.; Kretz...schmar 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; Ser...videi 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. Pocc...hiari; 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.; Reynol...ds 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