SAVERIONI, DANIELA
SAVERIONI, DANIELA
DIPARTIMENTO DI SCIENZE BIOMEDICHE E NEUROMOTORIE
Analyses of Protease Resistance and Aggregation State of Abnormal Prion Protein across the Spectrum of Human Prions
2013 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 Cescatti, Maura; Saverioni, Daniela; Capellari, Sabina; Tagliavini, Fabrizio; Kitamoto, Tetsuyuki; Ironside, James; Giese, Armin; Parchi, Piero
Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature
2017 Rossi, Marcello; Saverioni, Daniela; Di Bari, Michele; Baiardi, Simone; Lemstra, Afina Willemina; Pirisinu, Laura; Capellari, Sabina; Rozemuller, Annemieke; Nonno, Romolo; Parchi, Piero
Atypical neuropathological sCJD-MM phenotype with abundant white matter Kuru-type plaques sparing the cerebellar cortex.
2013 Gelpi E.; Soler Insa J.M.; Parchi P.; Saverioni D.; Yagüe J.; Nos C.; Martínez-Saez E.; Ribalta T.; Ferrer I.; Sanchez-Valle R.
Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA.
2012 Parchi P.; de Boni L.; Saverioni D.; Cohen M.L.; Ferrer I.; Gambetti P.; Gelpi E.; Giaccone G.; Hauw J.J.; Höftberger R.; Ironside J.W.; Jansen C.; Kovacs G.G.; Rozemuller A.; Seilhean D.; Tagliavini F.; Giese A.; Kretzschmar H.A.
Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: Insights into phenotypic variability and disease pathogenesis.
2011 Capellari S.; Strammiello R.; Saverioni D.; Kretzschmar H.; Parchi P.
Molecular pathology, classification, and diagnosis of sporadic human prion disease variants.
2012 Parchi P.; Saverioni D.
Prion protein misfolding, strains, and neurotoxicity: an update from studies on Mammalian prions.
2013 I. Poggiolini;D. Saverioni;P. Parchi
Transmission properties of atypical Creutzfeldt-Jakob disease: A clue to disease etiology?
2015 Kobayashi, Atsushi; Parchi, Piero; Yamada, Masahito; Brown, Paul; Saverioni, Daniela; Matsuura, Yuichi; Takeuchi, Atsuko; Mohri, Shirou; Kitamoto, Tetsuyuki
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| 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 | - |
| Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature | Rossi, Marcello; Saverioni, Daniela; Di Bari, Michele; Baiardi, Simone; Lemstra, Afina Willemina;... Pirisinu, Laura; Capellari, Sabina; Rozemuller, Annemieke; Nonno, Romolo; Parchi, Piero | 2017-01-01 | ACTA NEUROPATHOLOGICA COMMUNICATIONS | - | 1.01 Articolo in rivista | 2017 Rossi et al ANC.pdf |
| Atypical neuropathological sCJD-MM phenotype with abundant white matter Kuru-type plaques sparing the cerebellar cortex. | Gelpi E.; Soler Insa J.M.; Parchi P.; Saverioni D.; Yagüe J.; Nos C.; Martínez-Saez E.; Ribalta T....; Ferrer I.; Sanchez-Valle R. | 2013-01-01 | NEUROPATHOLOGY | - | 1.01 Articolo in rivista | - |
| Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA. | Parchi P.; de Boni L.; Saverioni D.; Cohen M.L.; Ferrer I.; Gambetti P.; Gelpi E.; Giaccone G.; H...auw J.J.; Höftberger R.; Ironside J.W.; Jansen C.; Kovacs G.G.; Rozemuller A.; Seilhean D.; Tagliavini F.; Giese A.; Kretzschmar H.A. | 2012-01-01 | ACTA NEUROPATHOLOGICA | - | 1.01 Articolo in rivista | - |
| Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: Insights into phenotypic variability and disease pathogenesis. | Capellari S.; Strammiello R.; Saverioni D.; Kretzschmar H.; Parchi P. | 2011-01-01 | ACTA NEUROPATHOLOGICA | - | 1.01 Articolo in rivista | - |
| Molecular pathology, classification, and diagnosis of sporadic human prion disease variants. | Parchi P.; Saverioni D. | 2012-01-01 | FOLIA NEUROPATHOLOGICA | - | 1.01 Articolo in rivista | - |
| Prion protein misfolding, strains, and neurotoxicity: an update from studies on Mammalian prions. | I. Poggiolini;D. Saverioni;P. Parchi | 2013-01-01 | INTERNATIONAL JOURNAL OF CELL BIOLOGY | - | 1.01 Articolo in rivista | - |
| Transmission properties of atypical Creutzfeldt-Jakob disease: A clue to disease etiology? | Kobayashi, Atsushi; Parchi, Piero; Yamada, Masahito; Brown, Paul; Saverioni, Daniela; Matsuura, Y...uichi; Takeuchi, Atsuko; Mohri, Shirou; Kitamoto, Tetsuyuki | 2015-01-01 | JOURNAL OF VIROLOGY | - | 1.01 Articolo in rivista | - |