Sporadic Creutzfeldt-Jakob disease in the United Kingdom: analysis of epidemiological surveillance data for 1970-96
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Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob diseaseImplications for Creutzfeldt-Jakob disease (CJD) in dentistry: a review of current knowledge.Quality evaluation for the surveillance system of human prion diseases in China based on the data from 2010 to 2016.The release of prion protein from platelets during storage of apheresis platelets.Voltage-gated potassium channel autoimmunity mimicking creutzfeldt-jakob disease.Prion diseases--an evidence-based protocol for infection control.Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United KingdomExtent of misclassification of death from Creutzfeldt-Jakob disease in England 1979-96: retrospective examination of clinical recordsA polymorphism in the regulatory region of PRNP is associated with increased risk of sporadic Creutzfeldt-Jakob diseaseCreutzfeldt-Jakob disease and haemophilia: assessment of risk.The pig as a source of cardiac xenografts.Diagnostic profiles of patients with late-onset Creutzfeldt-Jakob disease differ from those of younger Creutzfeldt-Jakob patients: a historical cohort study using data from the German National Reference Center.Ophthalmic surgery and Creutzfeldt-Jakob diseaseCreutzfeldt-Jakob disease in SwedenPrion diseases: current understanding of epidemiology and pathogenesis, and therapeutic advances.Creutzfeldt-Jakob disease and blood transfusion: results of the UK Transfusion Medicine Epidemiological Review study.From mad cows to sensible blood transfusion: the risk of prion transmission by labile blood components in the United Kingdom and in France.Incidence of Creutzfeldt-Jakob disease in Taiwan: a prospective 10-year surveillance.Creutzfeldt-Jakob disease and blood transfusion: updated results of the UK Transfusion Medicine Epidemiology Review Study.Sporadic and Infectious Human Prion Diseases.BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein.Clinical and laboratory features of 14 young Chinese probable sCJD patients.Estimated compliance for removal of specified risk materials from 18 U.S. beef packing plants.EFSA QRA Report 2004 (BIOHAZ) on quantitative assessment of the residual BSE risk in Bovine-derived productsApplication of a time-resolved fluoroimmunoassay for the analysis of normal prion protein in human blood and its components.Comparison Between Sporadic and Misdiagnosed Sporadic Creutzfeldt-Jakob Disease: A Report of Two Cases.Creutzfeldt-Jakob disease mortality in Canada, 1998 to 2013.
P2860
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P2860
Sporadic Creutzfeldt-Jakob disease in the United Kingdom: analysis of epidemiological surveillance data for 1970-96
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Sporadic Creutzfeldt-Jakob dis ...... surveillance data for 1970-96
@ast
Sporadic Creutzfeldt-Jakob dis ...... surveillance data for 1970-96
@en
type
label
Sporadic Creutzfeldt-Jakob dis ...... surveillance data for 1970-96
@ast
Sporadic Creutzfeldt-Jakob dis ...... surveillance data for 1970-96
@en
prefLabel
Sporadic Creutzfeldt-Jakob dis ...... surveillance data for 1970-96
@ast
Sporadic Creutzfeldt-Jakob dis ...... surveillance data for 1970-96
@en
P2093
P356
P1433
P1476
Sporadic Creutzfeldt-Jakob dis ...... surveillance data for 1970-96
@en
P2093
J W Wilesmith
R De Silva
S N Cousens
T F Esmonde
P304
P356
10.1136/BMJ.315.7105.389
P407
P577
1997-08-01T00:00:00Z