Maurizio Pocchiari
Maurizio Pocchiari
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A new variant of Creutzfeldt-Jakob disease in the UK
RG Will, JW Ironside, M Zeidler, K Estibeiro, SN Cousens, PG Smith, ...
The Lancet 347 (9006), 921-925, 1996
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
I Zerr, K Kallenberg, DM Summers, C Romero, A Taratuto, U Heinemann, ...
Brain 132 (10), 2659-2668, 2009
Iatrogenic Creutzfeldt–Jakob disease at the millennium
P Brown, M Preece, JP Brandel, T Sato, L McShane, I Zerr, A Fletcher, ...
Neurology 55 (8), 1075-1081, 2000
Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt–Jakob disease
I Zerr, M Pocchiari, S Collins, JP Brandel, J de Pedro Cuesta, RSG Knight, ...
Neurology 55 (6), 811-815, 2000
Genetic prion disease: the EUROCJD experience
GG Kovacs, M Puopolo, A Ladogana, M Pocchiari, H Budka, C van Duijn, ...
Human genetics 118 (2), 166-174, 2005
Mortality from Creutzfeldt–Jakob disease and related disorders in Europe, Australia, and Canada
A Ladogana, M Puopolo, EA Croes, H Budka, C Jarius, S Collins, ...
Neurology 64 (9), 1586-1591, 2005
Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt–Jakob disease
SJ Collins, P Sanchez-Juan, CL Masters, GM Klug, C van Duijn, ...
Brain 129 (9), 2278-2287, 2006
Iatrogenic Creutzfeldt-Jakob disease, final assessment
P Brown, JP Brandel, T Sato, Y Nakamura, J MacKenzie, RG Will, ...
Emerging infectious diseases 18 (6), 901, 2012
Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease.
A Alperovitch, I Zerr, M Pocchiari
The Lancet 353 (9165), 1673-1674, 1999
A test for Creutzfeldt–Jakob disease using nasal brushings
CD Orr˙, M Bongianni, G Tonoli, S Ferrari, AG Hughson, BR Groveman, ...
New England Journal of Medicine 371 (6), 519-529, 2014
Predictors of survival in sporadic Creutzfeldt–Jakob disease and other human transmissible spongiform encephalopathies
M Pocchiari, M Puopolo, EA Croes, H Budka, E Gelpi, S Collins, V Lewis, ...
Brain 127 (10), 2348-2359, 2004
Phenotypic variability of Gerstmann-Strńussler-Scheinker disease is associated with prion protein heterogeneity
P Piccardo, SR Dlouhy, PMJ Lievens, K Young, D Phil, TD Bird, D Nochlin, ...
Journal of neuropathology and experimental neurology 57 (10), 979-988, 1998
Congo red prolongs the incubation period in scrapie-infected hamsters.
L Ingrosso, A Ladogana, M Pocchiari
Journal of virology 69 (1), 506-508, 1995
Efficient transmission and characterization of Creutzfeldt–Jakob disease strains in bank voles
R Nonno, MA Di Bari, F Cardone, G Vaccari, P Fazzi, G Dell'Omo, ...
PLoS pathogens 2 (2), e12, 2006
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 (5), 659-671, 2009
Descriptive epidemiology of Creutzfeldt‐Jakob disease in six european countries, 1993–1995
RG Will, A Alperovitch, S Poser, M Pocchiari, A Hofman, E Mitrova, ...
Annals of neurology 43 (6), 763-767, 1998
Amphotericin B treatment dissociates in vivo replication of the scrapie agent from PrP accumulation
YG Xi, L Ingrosso, A Ladogana, C Masullo, M Pocchiari
Nature 356 (6370), 598-601, 1992
Pre-symptomatic detection of prions by cyclic amplification of protein misfolding
C Soto, L Anderes, S Suardi, F Cardone, J Castilla, MJ Frossard, S Peano, ...
FEBS letters 579 (3), 638-642, 2005
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt–Jakob disease
G Zanusso, S Ferrari, F Cardone, P Zampieri, M Gelati, M Fiorini, ...
New England Journal of Medicine 348 (8), 711-719, 2003
Iatrogenic Creutzfeldt‐Jakob disease An example of the interplay between ancient genes and modern medicine
P Brown, L Cervenakova, LG Goldfarb, WR McCombie, R Rubenstein, ...
Neurology 44 (2), 291-291, 1994
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