Sabina Capellari
Sabina Capellari
Dipartimento di Scienze Biomediche e Neuromotorie, Universitā di Bologna e IRCCS ISNB, Bologna
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Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects
P Parchi, A Giese, S Capellari, P Brown, W Schulz‐Schaeffer, O Windl, ...
Annals of neurology 46 (2), 224-233, 1999
Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease
P Parchi, R Castellani, S Capellari, B Ghetti, K Young, SG Chen, M Farlow, ...
Annals of neurology 39 (6), 767-778, 1996
Quantifying prion disease penetrance using large population control cohorts
EV Minikel, SM Vallabh, M Lek, K Estrada, KE Samocha, ...
Science translational medicine 8 (322), 322ra9-322ra9, 2016
Genetic influence on the structural variations of the abnormal prion protein
P Parchi, W Zou, W Wang, P Brown, S Capellari, B Ghetti, N Kopp, ...
Proceedings of the National Academy of Sciences 97 (18), 10168-10172, 2000
Typing prion isoforms.
P Parchi, S Capellari, SG Chen, RB Petersen, P Gambetti, N Kopp, ...
Skin nerve α-synuclein deposits: a biomarker for idiopathic Parkinson disease
V Donadio, A Incensi, V Leta, MP Giannoccaro, C Scaglione, P Martinelli, ...
Neurology 82 (15), 1362-1369, 2014
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
DJH Moss, AF Pardiņas, D Langbehn, K Lo, BR Leavitt, R Roos, A Durr, ...
The Lancet Neurology 16 (9), 701-711, 2017
Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification
P Parchi, R Strammiello, S Notari, A Giese, JPM Langeveld, A Ladogana, ...
Acta neuropathologica 118, 659-671, 2009
Variably protease‐sensitive prionopathy: a new sporadic disease of the prion protein
WQ Zou, G Puoti, X Xiao, J Yuan, L Qing, I Cali, M Shimoji, ...
Annals of neurology 68 (2), 162-172, 2010
Ultrasensitive RT-QuIC assay with high sensitivity and specificity for Lewy body-associated synucleinopathies
M Rossi, N Candelise, S Baiardi, S Capellari, G Giannini, CD Orrų, ...
Acta neuropathologica 140, 49-62, 2020
Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann–Sträussler–Scheinker disease
P Parchi, SG Chen, P Brown, W Zou, S Capellari, H Budka, J Hainfellner, ...
Proceedings of the National Academy of Sciences 95 (14), 8322-8327, 1998
A subtype of sporadic prion disease mimicking fatal familial insomnia
P Parchi, S Capellari, S Chin, HB Schwarz, NP Schecter, JD Butts, ...
Neurology 52 (9), 1757-1757, 1999
Mixed brain pathologies in dementia: the BrainNet Europe consortium experience
GG Kovacs, I Alafuzoff, S Al-Sarraj, T Arzberger, N Bogdanovic, ...
Dementia and geriatric cognitive disorders 26 (4), 343-350, 2008
Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease
RJ Castellani, M Colucci, Z Xie, W Zou, C Li, P Parchi, S Capellari, ...
Neurology 63 (3), 436-442, 2004
Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease
G Rizzo, P Martinelli, D Manners, C Scaglione, C Tonon, P Cortelli, ...
Brain 131 (10), 2690-2700, 2008
High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions
A Franceschini, S Baiardi, AG Hughson, N McKenzie, F Moda, M Rossi, ...
Scientific reports 7 (1), 10655, 2017
Inherited prion diseases
Q Kong, WK Surewicz, RB Petersen, W Zou, SG Chen, P Gambetti, ...
Prion biology and diseases, 673-776, 2004
Effects of formalin fixation, paraffin embedding, and time of storage on DNA preservation in brain tissue: a BrainNet Europe study
I Ferrer, J Armstrong, S Capellari, P Parchi, T Arzberger, J Bell, H Budka, ...
Brain Pathology 17 (3), 297-303, 2007
Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of …
F Lattanzio, S Abu-Rumeileh, A Franceschini, H Kai, G Amore, I Poggiolini, ...
Acta Neuropathologica 133, 559-578, 2017
A genome-wide association study in multiple system atrophy
A Sailer, SW Scholz, MA Nalls, C Schulte, M Federoff, TR Price, A Lees, ...
Neurology 87 (15), 1591-1598, 2016
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