نتائج البحث - Silvio Notari
- يعرض 1 - 10 نتائج من 10
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A refined method for molecular typing reveals that co-occurrence of PrPSc types in Creutzfeldt–Jakob disease is not the rule حسب Silvio Notari, Sabina Capellari, Jan Langeveld, Armin Giese, Rosaria Strammiello, Pierluigi Gambetti, Hans A. Kretzschmar, Piero Parchi
منشور في 2007Artigo -
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Effects of Different Experimental Conditions on the PrPSc Core Generated by Protease Digestion حسب Silvio Notari, Sabina Capellari, Armin Giese, Ingo M. Westner, Agostino Baruzzi, Bernardino Ghetti, Pierluigi Gambetti, Hans A. Kretzschmar, Piero Parchi
منشور في 2004Artigo -
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Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease حسب Piero Parchi, Maura Cescatti, Silvio Notari, Walter Schulz‐Schaeffer, Sabina Capellari, Armin Giese, Wen‐Quan Zou, H. A. Kretzschmar, Bernardino Ghetti, Patrick O. Brown
منشور في 2010Artigo -
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Characterization of Truncated Forms of Abnormal Prion Protein in Creutzfeldt-Jakob Disease حسب Silvio Notari, Rosaria Strammiello, Sabina Capellari, Armin Giese, Maura Cescatti, Jacques Grassi, Bernardino Ghetti, Jan Langeveld, Wen‐Quan Zou, Pierluigi Gambetti, Hans A. Kretzschmar, Piero Parchi
منشور في 2008Artigo -
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Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification حسب Piero Parchi, Rosaria Strammiello, Silvio Notari, Armin Giese, Jan Langeveld, Anna Ladogana, Inga Zerr, Federico Roncaroli, P. Cras, Bernardino Ghetti, Maurizio Pocchiari, Hans A. Kretzschmar, Sabina Capellari
منشور في 2009Artigo -
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Multiorgan Detection and Characterization of Protease-Resistant Prion Protein in a Case of Variant CJD Examined in the United States حسب Silvio Notari, Francisco J. Moleres, Stephen Hunter, Ermias D. Belay, Lawrence B. Schonberger, Ignazio Calì, Piero Parchi, Wun‐Ju Shieh, Paul Brown, Sherif R. Zaki, Wen-Quan Zou, Pierluigi Gambetti
منشور في 2010Artigo -
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Transmission Characteristics of Variably Protease-Sensitive Prionopathy حسب Silvio Notari, Xiangzhu Xiao, Juan Carlos Espinosa, Yvonne Cohen, Liuting Qing, Patricia Aguilar‐Calvo, Diane Kofskey, Ignazio Calì, Laura Cracco, Qingzhong Kong, Juan María Torres, Wen‐Quan Zou, Pierluigi Gambetti
منشور في 2014Artigo -
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Prions in the Urine of Patients with Variant Creutzfeldt–Jakob Disease حسب Fabio Moda, Pierluigi Gambetti, Silvio Notari, Luis Concha‐Marambio, Marcella Catania, Kyung-Won Park, Emanuela Maderna, Silvia Suardi, Stéphane Haı̈k, J.-P. Brandel, James W. Ironside, Richard Knight, Fabrizio Tagliavini, Claudio Soto
منشور في 2014Artigo -
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Variably protease‐sensitive prionopathy: A new sporadic disease of the prion protein حسب Wen‐Quan Zou, Gianfranco Puoti, Xiangzhu Xiao, Jue Yuan, Liuting Qing, Ignazio Calì, Miyuki Shimoji, Jan Langeveld, Rudy J. Castellani, Silvio Notari, Barbara J. Crain, Robert E. Schmidt, Michael D. Geschwind, Stephen J. DeArmond, Nigel J. Cairns, Dennis W. Dickson, Lawrence S. Honig, Juan María Torres, James A. Mastrianni, Sabina Capellari, Giorgio Giaccone, Ermias D. Belay, Lawrence B. Schonberger, Mark L. Cohen, George Perry, Qingzhong Kong, Piero Parchi, Fabrizio Tagliavini, Pierluigi Gambetti
منشور في 2010Artigo
أدوات البحث:
موضوعات ذات صلة
Disease
Medicine
Pathology
Biology
Virology
Prion protein
Creutzfeldt-Jakob Syndrome
Gene
Genetics
Biochemistry
Enzyme
Phenotype
Protease
Chemistry
Electrical engineering
Engineering
Genotype
Transmission (telecommunications)
Internal medicine
Physics
Allele
Amino acid
Antibody
Bovine spongiform encephalopathy
Chromatography
Cleavage (geology)
Composite material
Confidence interval
Core (optical fiber)
Digestion (alchemy)