Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJD.
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Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects.Clinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests.[A retrospective study of Creutzfeldt-Jakob disease in North of Portugal 1993-2002: demographic, clinical and neuropathological features].Prion diseases--an evidence-based protocol for infection control.Source of variant Creutzfeldt-Jakob disease outside United Kingdom.Dietary Risk Factors for Sporadic Creutzfeldt-Jakob Disease: A Confirmatory Case-Control Study.vCJD: the epidemic that never was. New variant Creutzfeldt-Jakob disease: the critique that never wasLaboratory diagnosis of variant Creutzfeldt-Jakob disease.Can mortality data provide reliable indicators for Creutzfeldt-Jakob disease surveillance? A study in France from 2000 to 2008.Human prion diseases.Presenile dementia syndromes: an update on taxonomy and diagnosis.Prion diseases: epidemiology in man.Seeded fibrillation as molecular basis of the species barrier in human prion diseases.Overview and evaluation of 15 years of Creutzfeldt-Jakob disease surveillance in Belgium, 1998-2012.Requirements for mutant and wild-type prion protein misfolding in vitro.An overview of transmissible spongiform encephalopathies.Raised CSF phospho-tau concentrations in variant Creutzfeldt-Jakob disease: diagnostic and pathological implications.Managing the risk of transmission of variant Creutzfeldt Jakob disease by blood products.Decontamination and CJD: the latest guidance.Recent developments in mucosal vaccines against prion diseases.Ethics in prion disease.Mortality from dementia in occupations at risk of exposure to bovine spongiform encephalopathy: analysis of death registrationsMolecular pathology of human prion diseases.Review: Laboratory diagnosis and surveillance of Creutzfeldt-Jakob disease.BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein.Prospective 10-year surveillance of human prion diseases in Japan.Transmission of sporadic Creutzfeldt-Jakob disease by blood transfusion: risk factor or possible biases.First symptom and initial diagnosis in sporadic CJD patients in Germany.Spatial pattern of prion protein deposits in patients with sporadic Creutzfeldt-Jakob disease.Epidemiological study of Creutzfeldt-Jakob disease death certificates in Canada, 1979-2001.Creutzfeldt-Jakob disease in Mexico.
P2860
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P2860
Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJD.
description
1998 nî lūn-bûn
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1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Descriptive epidemiology of Cr ...... aborative Study Group for CJD.
@en
type
label
Descriptive epidemiology of Cr ...... aborative Study Group for CJD.
@en
prefLabel
Descriptive epidemiology of Cr ...... aborative Study Group for CJD.
@en
P2093
P2860
P356
P1433
P1476
Descriptive epidemiology of Cr ...... aborative Study Group for CJD.
@en
P2093
Alperovitch A
D'Alessandro M
Delasnerie-Laupretre N
Pocchiari M
de Silva R
P2860
P304
P356
10.1002/ANA.410430611
P577
1998-06-01T00:00:00Z