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Silvio Notari

Showing results (1-10 of 28) with videos related to

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Handbook of Clinical Neurology|June 12, 2018
Variably protease-sensitive prionopathySilvio Notari, Brian S Appleby, Pierluigi Gambetti
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 29, 2019
Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplificationManuel V Camacho, Glenn Telling, Qingzhong Kong, et al.
Acta Neuropathologica|November 9, 2010
Molecular biology and pathology of prion strains in sporadic human prion diseasesPierluigi Gambetti, Ignazio Cali, Silvio Notari, et al.
The Journal of Biological Chemistry|July 31, 2013
Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prionsDaniela Saverioni, Silvio Notari, Sabina Capellari, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 26, 2007
A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the ruleSilvio Notari, Sabina Capellari, Jan Langeveld, et al.
The Journal of Biological Chemistry|February 3, 2004
Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJDSilvio Notari, Sabina Capellari, Armin Giese, et al.
Acta Neuropathologica Communications|May 31, 2019
Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragmentsLaura Cracco, Xiangzhu Xiao, Satish K Nemani, et al.
Annals of Clinical and Translational Neurology|October 10, 2023
Detection of prions in the urine of patients affected by sporadic Creutzfeldt-Jakob diseaseSandra Pritzkow, Frank Ramirez, Adam Lyon, et al.
Movement Disorders Clinical Practice|September 13, 2016
Clinicopathological Correlates in a <i>PRNP</i> P102L Mutation Carrier with Rapidly Progressing Parkinsonism-dystoniaChizoba C Umeh, Piyush Kalakoti, Michael K Greenberg, et al.
Scientific Reports|March 28, 2019
PMCA-replicated PrP<sup>D</sup> in urine of vCJD patients maintains infectivity and strain characteristics of brain PrP<sup>D</sup>: Transmission studyIgnazio Cali, Jody Lavrich, Fabio Moda, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Handbook of Clinical Neurology|June 12, 2018
Variably protease-sensitive prionopathySilvio Notari, Brian S Appleby, Pierluigi Gambetti
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 29, 2019
Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplificationManuel V Camacho, Glenn Telling, Qingzhong Kong, et al.
Acta Neuropathologica|November 9, 2010
Molecular biology and pathology of prion strains in sporadic human prion diseasesPierluigi Gambetti, Ignazio Cali, Silvio Notari, et al.
The Journal of Biological Chemistry|July 31, 2013
Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prionsDaniela Saverioni, Silvio Notari, Sabina Capellari, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 26, 2007
A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the ruleSilvio Notari, Sabina Capellari, Jan Langeveld, et al.
The Journal of Biological Chemistry|February 3, 2004
Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJDSilvio Notari, Sabina Capellari, Armin Giese, et al.
Acta Neuropathologica Communications|May 31, 2019
Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragmentsLaura Cracco, Xiangzhu Xiao, Satish K Nemani, et al.
Annals of Clinical and Translational Neurology|October 10, 2023
Detection of prions in the urine of patients affected by sporadic Creutzfeldt-Jakob diseaseSandra Pritzkow, Frank Ramirez, Adam Lyon, et al.
Movement Disorders Clinical Practice|September 13, 2016
Clinicopathological Correlates in a <i>PRNP</i> P102L Mutation Carrier with Rapidly Progressing Parkinsonism-dystoniaChizoba C Umeh, Piyush Kalakoti, Michael K Greenberg, et al.
Scientific Reports|March 28, 2019
PMCA-replicated PrP<sup>D</sup> in urine of vCJD patients maintains infectivity and strain characteristics of brain PrP<sup>D</sup>: Transmission studyIgnazio Cali, Jody Lavrich, Fabio Moda, et al.
Pageof 3