Silvio Notari

Università di Bologna, Bologna, Italy 
"Silvio Notari"
Mean distance: 17.19 (cluster 28)
Cross-listing: Neuropathology Tree

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Cracco L, Cali I, Cohen ML, et al. (2023) Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host. Brain : a Journal of Neurology
Pritzkow S, Ramirez F, Lyon A, et al. (2023) Detection of prions in the urine of patients affected by sporadic Creutzfeldt-Jakob disease. Annals of Clinical and Translational Neurology
Nemani SK, Xiao X, Cali I, et al. (2020) A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease. Acta Neuropathologica Communications. 8: 85
Camacho MV, Telling G, Kong Q, et al. (2019) Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplification. Laboratory Investigation; a Journal of Technical Methods and Pathology
Cracco L, Xiao X, Nemani SK, et al. (2019) Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments. Acta Neuropathologica Communications. 7: 1
Cali I, Lavrich J, Moda F, et al. (2019) PMCA-replicated PrP in urine of vCJD patients maintains infectivity and strain characteristics of brain PrP: Transmission study. Scientific Reports. 9: 5191
Nonno R, Notari S, Di Bari MA, et al. (2019) Variable Protease-Sensitive Prionopathy Transmission to Bank Voles. Emerging Infectious Diseases. 25: 73-81
Nemani SK, Notari S, Cali I, et al. (2018) Co-occurrence of chronic traumatic encephalopathy and prion disease. Acta Neuropathologica Communications. 6: 140
Notari S, Appleby BS, Gambetti P. (2018) Variably protease-sensitive prionopathy. Handbook of Clinical Neurology. 153: 175-190
Cracco L, Notari S, Cali I, et al. (2017) Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type. Scientific Reports. 7: 38280
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