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Piero Parchi
Piero Parchi
University of Bologna and IRCCS Istituto delle Scienze Neurologiche di Bologna
Verified email at unibo.it
Title
Cited by
Cited by
Year
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
16021999
Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity
GC Telling, P Parchi, SJ DeArmond, P Cortelli, P Montagna, R Gabizon, ...
Science 274 (5295), 2079-2082, 1996
10431996
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
10161996
Sporadic and familial CJD: classification and characterisation
P Gambetti, Q Kong, W Zou, P Parchi, SG Chen
British medical bulletin 66 (1), 213-239, 2003
6752003
Truncated forms of the human prion protein in normal brain and in prion diseases
SG Chen, DB Teplow, P Parchi, JK Teller, P Gambetti, L Autilio-Gambetti
Journal of Biological Chemistry 270 (32), 19173-19180, 1995
5971995
Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium
I Alafuzoff, T Arzberger, S Al‐Sarraj, I Bodi, N Bogdanovic, H Braak, ...
Brain pathology 18 (4), 484-496, 2008
4632008
CSF biomarker variability in the Alzheimer's Association quality control program
N Mattsson, U Andreasson, S Persson, MC Carrillo, S Collins, S Chalbot, ...
Alzheimer's & Dementia 9 (3), 251-261, 2013
3962013
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.
L Monari, SG Chen, P Brown, P Parchi, RB Petersen, J Mikol, F Gray, ...
Proceedings of the National Academy of Sciences 91 (7), 2839-2842, 1994
3951994
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
3592016
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
3402000
Staging/typing of Lewy body related α-synuclein pathology: a study of the BrainNet Europe Consortium
I Alafuzoff, PG Ince, T Arzberger, S Al-Sarraj, J Bell, I Bodi, N Bogdanovic, ...
Acta neuropathologica 117, 635-652, 2009
3172009
Typing prion isoforms.
P Parchi, S Capellari, SG Chen, RB Petersen, P Gambetti, N Kopp, ...
3101997
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
2702009
Fatal familial insomnia and familial Creutzfeldt‐Jakob disease: clinical, pathological and molecular features
P Gambetti, P Parchi, RB Petersen, SG Chen, E Lugaresi
Brain pathology 5 (1), 43-51, 1995
2661995
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
2642010
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 Orrù, ...
Acta neuropathologica 140, 49-62, 2020
2462020
Tau gene mutation in familial progressive subcortical gliosis
M Goedert, MG Spillantini, RA Crowther, SG Chen, P Parchi, M Tabaton, ...
Nature Medicine 5 (4), 454-457, 1999
2441999
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
2341998
Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA
P Parchi, L De Boni, D Saverioni, ML Cohen, I Ferrer, P Gambetti, E Gelpi, ...
Acta neuropathologica 124, 517-529, 2012
2192012
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
2111999
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