Search research articles
Contact Us
Filters
Showing results (21-30 of 28) with videos related to
Page
of 3
Sort By:
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-Old
Nupur 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 type
Laura 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 States
Silvio 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 disease
Fabio Moda, Pierluigi Gambetti, Silvio Notari, et al.
Acta Neuropathologica Communications
|
June 21, 2020
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease
Satish 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 patients
Franco 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 Consortium
Piero Parchi, Silvio Notari, Petra Weber, et al.
Annals of Neurology
|
August 10, 2010
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein
Wen-Quan Zou, Gianfranco Puoti, Xiangzhu Xiao, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 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-Old
Nupur 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 type
Laura 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 States
Silvio 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 disease
Fabio Moda, Pierluigi Gambetti, Silvio Notari, et al.
Acta Neuropathologica Communications
|
June 21, 2020
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease
Satish 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 patients
Franco 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 Consortium
Piero Parchi, Silvio Notari, Petra Weber, et al.
Annals of Neurology
|
August 10, 2010
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein
Wen-Quan Zou, Gianfranco Puoti, Xiangzhu Xiao, et al.
Page
of 3