CAPELLARI, SABINA

CAPELLARI, SABINA  

DIPARTIMENTO DI SCIENZE BIOMEDICHE E NEUROMOTORIE  

Docenti di ruolo di IIa fascia  

Capellari S; S. Capellari; Sabina Capellari  

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Risultati 1 - 20 di 197 (tempo di esecuzione: 0.044 secondi).
Titolo Autore(i) Anno Periodico Editore Tipo File
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 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) -
Abnormal in vivo cerebral energy metabolism in Huntington’s disease: preliminary findings G Rizzo; C Tonon; E Malucelli; C Scaglione; C Testa; D Manners; S Capellari; P Cortelli; R Lodi 2011-01-01 NEUROLOGICAL SCIENCES - 4.01 Contributo in Atti di convegno -
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'' 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 -
Allele-specific silencing as treatment for gene duplication disorders: Proof-of-principle in autosomal dominant leukodystrophy Giorgio E.; Lorenzati M.; Di Val Cervo P.R.; Brussino A.; Cernigoj M.; Sala E.D.; Stella A.B.; Ferrero M.; Caiazzo M.; Capellari S.; Cortelli P.; Conti L.; Cattaneo E.; Buffo A.; Brusco A. 2019-01-01 BRAIN - 1.01 Articolo in rivista -
Alterazione del metabolismo energetico cerebrale in vivo nella malattia di Huntington: dati preliminari G. Rizzo; C. Tonon; E. Malucelli; C. Scaglione; C. Testa; D. Manners; S. Capellari; R. Lodi; P. Cortelli. 2011-01-01 - - 4.02 Riassunto (Abstract) -
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 LMNB1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele-Specific Expression. E. Giorgio;H. Rolyan;L. Kropp;A. B. Chakka;S. Yatsenko;E. D. Gregorio;D. Lacerenza;G. Vaula;F. Talarico;P. Mandich;C. Toro;E. E. Pierre;P. Labauge;S. Capellari;P. Cortelli;F. P. Vairo;D. Miguel;D. Stubbolo;L. C. Marques;W. Gahl;O. Boespflug-Tanguy;A. Melberg;S. Hassin-Baer;O. S. Cohen;R. Pjontek;A. Grau;T. Klopstock;B. Fogel;I. Meijer;G. Rouleau;J. L. Bouchard;M. Ganapathiraju;A. Vanderver;N. Dahl;G. Hobson;A. Brusco;A. Brussino;Q. S. Padiath 2013-01-01 HUMAN MUTATION - 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