Variant CJD. 18 years of research and surveillance. - Wikidata - wikimedia - TriplyDB

Variant CJD. 18 years of research and surveillance.

Variant CJD. 18 years of research and surveillance.

http://www.wikidata.org/entity/Q34453109

about

Epidemiological characteristics of human prion diseases Improving platelet transfusion safety: biomedical and technical considerations Silent Prions and Covert Prion Transmission Analysis of Conformational Stability of Abnormal Prion Protein Aggregates across the Spectrum of Creutzfeldt-Jakob Disease Prions Human prion diseases: surgical lessons learned from iatrogenic prion transmission Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease.Recent US Case of Variant Creutzfeldt-Jakob Disease-Global Implications.Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone.Overview and evaluation of 15 years of Creutzfeldt-Jakob disease surveillance in Belgium, 1998-2012.Rapid and Highly Sensitive Detection of Variant Creutzfeldt-Jakob Disease Abnormal Prion Protein on Steel Surfaces by Protein Misfolding Cyclic Amplification: Application to Prion Decontamination Studies.Increased Abundance of M Cells in the Gut Epithelium Dramatically Enhances Oral Prion Disease Susceptibility The influence of PRNP polymorphisms on human prion disease susceptibility: an update.Prion disease pathogenesis in the absence of the commensal microbiota.A case cluster of variant Creutzfeldt-Jakob disease linked to the Kingdom of Saudi Arabia.Developing Therapeutics for PrP Prion Diseases.Infectious Agents in Bovine Red Meat and Milk and Their Potential Role in Cancer and Other Chronic Diseases.Variant Creutzfeldt-Jakob disease deferral in Canada: impact of stop dates.The Risk of Prion Infection through Bovine Grafting Materials.A prion reduction filter does not completely remove endogenous prion infectivity from sheep blood.Prion Diagnosis: Application of Real-Time Quaking-Induced Conversion.How do PrPSc Prions Spread between Host Species, and within Hosts?Public health risks from subclinical variant CJD.Food safety challenges and One Health within Europe.Recombinant PrPSc shares structural features with brain-derived PrPSc: Insights from limited proteolysis.Prion Diseases.Generation of novel neuroinvasive prions following intravenous challenge.Creutzfeldt-Jakob disease mortality in Canada, 1998 to 2013.Oral Prion Neuroinvasion Occurs Independently of PrP Expression in the Gut Epithelium

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P2860

Variant CJD. 18 years of research and surveillance.

http://www.wikidata.org/entity/Q34453109

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2014 nî lūn-bûn

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2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Variant CJD. 18 years of research and surveillance.

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Variant CJD. 18 years of research and surveillance.

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Variant CJD. 18 years of research and surveillance.

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Variant CJD. 18 years of research and surveillance.

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Variant CJD. 18 years of research and surveillance.

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Variant CJD. 18 years of research and surveillance.

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Variant CJD. 18 years of research and surveillance.

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Variant CJD. 18 years of research and surveillance.

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Variant CJD. 18 years of research and surveillance.

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Aileen Boyle

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Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey

A novel human disease with abnormal prion protein sensitive to protease

Safety and efficacy of quinacrine in human prion disease (PRION-1 study): a patient-preference trial

All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJD

Variant Creutzfeldt-Jakob disease: an update

Variant Creutzfeldt-Jakob disease

Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob disease

The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob disease.

Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype.

Reduction of transmissible spongiform encephalopathy infectivity from human red blood cells with prion protein affinity ligands.

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