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Silvio Notari

Showing results (21-30 of 28) with videos related to

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Alzheimer Disease and Associated Disorders|May 22, 2014
Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-OldNupur Ghoshal, Arie Perry, Daniel McKeel, et al.
Scientific Reports|January 17, 2017
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion typeLaura Cracco, Silvio Notari, Ignazio Cali, et al.
Plos One|January 26, 2010
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United StatesSilvio Notari, Francisco J Moleres, Stephen B Hunter, et al.
The New England Journal of Medicine|August 8, 2014
Prions in the urine of patients with variant Creutzfeldt-Jakob diseaseFabio Moda, Pierluigi Gambetti, Silvio Notari, et al.
Acta Neuropathologica Communications|June 21, 2020
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob diseaseSatish K Nemani, Xiangzhu Xiao, Ignazio Cali, et al.
Biochemical and Biophysical Research Communications|December 3, 2014
Mutant PrPCJD prevails over wild-type PrPCJD in the brain of V210I and R208H genetic Creutzfeldt-Jakob disease patientsFranco Cardone, Serena Principe, Maria Eugenia Schininà, et al.
Brain Pathology (Zurich, Switzerland)|July 16, 2008
Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion ConsortiumPiero Parchi, Silvio Notari, Petra Weber, et al.
Annals of Neurology|August 10, 2010
Variably protease-sensitive prionopathy: a new sporadic disease of the prion proteinWen-Quan Zou, Gianfranco Puoti, Xiangzhu Xiao, et al.
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Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Alzheimer Disease and Associated Disorders|May 22, 2014
Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-OldNupur Ghoshal, Arie Perry, Daniel McKeel, et al.
Scientific Reports|January 17, 2017
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion typeLaura Cracco, Silvio Notari, Ignazio Cali, et al.
Plos One|January 26, 2010
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United StatesSilvio Notari, Francisco J Moleres, Stephen B Hunter, et al.
The New England Journal of Medicine|August 8, 2014
Prions in the urine of patients with variant Creutzfeldt-Jakob diseaseFabio Moda, Pierluigi Gambetti, Silvio Notari, et al.
Acta Neuropathologica Communications|June 21, 2020
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob diseaseSatish K Nemani, Xiangzhu Xiao, Ignazio Cali, et al.
Biochemical and Biophysical Research Communications|December 3, 2014
Mutant PrPCJD prevails over wild-type PrPCJD in the brain of V210I and R208H genetic Creutzfeldt-Jakob disease patientsFranco Cardone, Serena Principe, Maria Eugenia Schininà, et al.
Brain Pathology (Zurich, Switzerland)|July 16, 2008
Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion ConsortiumPiero Parchi, Silvio Notari, Petra Weber, et al.
Annals of Neurology|August 10, 2010
Variably protease-sensitive prionopathy: a new sporadic disease of the prion proteinWen-Quan Zou, Gianfranco Puoti, Xiangzhu Xiao, et al.
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