Silvio Notari
Affiliations: | Università di Bologna, Bologna, Italy |
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| 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 |
| Umeh CC, Kalakoti P, Greenberg MK, et al. (2016) Clinicopathological Correlates in a PRNP P102L Mutation Carrier with Rapidly Progressing Parkinsonism-dystonia. Movement Disorders Clinical Practice. 3: 355-358 |
| Ghoshal N, Perry A, McKeel D, et al. (2015) Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old. Alzheimer Disease and Associated Disorders. 29: 173-6 |