Silvio Notari

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

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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
Cardone F, Principe S, Schininà ME, et al. (2014) Mutant PrPCJD prevails over wild-type PrPCJD in the brain of V210I and R208H genetic Creutzfeldt-Jakob disease patients. Biochemical and Biophysical Research Communications. 454: 289-94
Notari S, Xiao X, Espinosa JC, et al. (2014) Transmission characteristics of variably protease-sensitive prionopathy. Emerging Infectious Diseases. 20: 2006-14
Moda F, Gambetti P, Notari S, et al. (2014) Prions in the urine of patients with variant Creutzfeldt-Jakob disease. The New England Journal of Medicine. 371: 530-9
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