Laboratory diagnosis of variant Creutzfeldt-Jakob disease.
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Neuropathology of non-Alzheimer degenerative disordersImplications for Creutzfeldt-Jakob disease (CJD) in dentistry: a review of current knowledge.Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob disease.PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar DegenerationPreclinical deposition of pathological prion protein PrPSc in muscles of hamsters orally exposed to scrapie.A protease-resistant prion protein isoform is present in urine of animals and humans affected with prion diseases.Variant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public healthDistinct stability states of disease-associated human prion protein identified by conformation-dependent immunoassayLaminar distribution of the pathological changes in sporadic and variant creutzfeldt-jakob diseaseMolecular pathology of human prion disease.A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature.Review: contribution of transgenic models to understanding human prion disease.Variant Creutzfeldt-Jakob disease: risk of transmission by blood transfusion and blood therapies.The transmissible spongiform encephalopathies (prion diseases): a review for dental surgeons.What is the basis of transmissible spongiform encephalopathy induced neurodegeneration and can it be repaired?Pathological diagnosis of variant Creutzfeldt-Jakob disease.Prion diseases: contribution of high-resolution immunomorphology.Mother to offspring transmission of chronic wasting disease in reeves' muntjac deer.Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease.The transmissible spongiform encephalopathies: pathogenic mechanisms and strategies for therapeutic intervention.Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study.Detection and localization of PrPSc in the skeletal muscle of patients with variant, iatrogenic, and sporadic forms of Creutzfeldt-Jakob diseaseVariant Creutzfeldt-Jakob disease and its transmission by blood.Prions and the oral cavity.Specificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt-Jakob disease.Prion infectivity in variant Creutzfeldt-Jakob disease rectum.Variant Creutzfeldt-Jakob disease: risk of transmission by blood and blood products.Application of Atomic Dielectric Resonance Spectroscopy for the screening of blood samples from patients with clinical variant and sporadic CJD.Raised CSF phospho-tau concentrations in variant Creutzfeldt-Jakob disease: diagnostic and pathological implications.Phenotypic variability in human prion diseases.In utero transmission and tissue distribution of chronic wasting disease-associated prions in free-ranging Rocky Mountain elkThe contribution of different prion protein types and host polymorphisms to clinicopathological variations in Creutzfeldt-Jakob disease.Comparative quantitative study of 'signature' pathological lesions in the hippocampus and adjacent gyri of 12 neurodegenerative disorders.Current issues in endoscope reprocessing and infection control during gastrointestinal endoscopy.Neuropathological changes in striate and extrastriate visual cortex in variant Creutzfeldt-Jakob disease (vCJD).Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote: atypical molecular phenotype.Quantification of vacuolation ("spongiform change"), surviving neurones and prion protein deposition in eleven cases of variant Creutzfeldt-Jakob disease.Neuronal and astrocytic responses involving the serotonergic system in human spongiform encephalopathies.
P2860
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P2860
Laboratory diagnosis of variant Creutzfeldt-Jakob disease.
description
2000 nî lūn-bûn
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2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Laboratory diagnosis of variant Creutzfeldt-Jakob disease.
@ast
Laboratory diagnosis of variant Creutzfeldt-Jakob disease.
@en
type
label
Laboratory diagnosis of variant Creutzfeldt-Jakob disease.
@ast
Laboratory diagnosis of variant Creutzfeldt-Jakob disease.
@en
prefLabel
Laboratory diagnosis of variant Creutzfeldt-Jakob disease.
@ast
Laboratory diagnosis of variant Creutzfeldt-Jakob disease.
@en
P2093
P2860
P1433
P1476
Laboratory diagnosis of variant Creutzfeldt-Jakob disease
@en
P2093
P2860
P356
10.1046/J.1365-2559.2000.00946.X
P577
2000-07-01T00:00:00Z