Clinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests.
about
A proposal of new diagnostic pathway for fatal familial insomniaRelationship between clinical signs and postmortem test status in cattle experimentally infected with the bovine spongiform encephalopathy agentQuality evaluation for the surveillance system of human prion diseases in China based on the data from 2010 to 2016.Impact of the clinical context on the 14-3-3 test for the diagnosis of sporadic CJD.Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob diseaseFamilial Creutzfeldt-Jakob disease with V180I mutation.Altered Prion protein expression pattern in CSF as a biomarker for Creutzfeldt-Jakob disease.The Features of Genetic Prion Diseases Based on Chinese Surveillance Program.Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.Current and future molecular diagnostics for prion diseases.Therapeutic approaches for prion disorders.14-3-3s are potential biomarkers for HIV-related neurodegeneration.De Novo Generation of a Unique Cervid Prion Strain Using Protein Misfolding Cyclic Amplification.EEG abnormalities in poikilothermia suggesting Creutzfeldt-Jakob disease.Targeting prion amyloid deposits in vivo.The associations of two SNPs in miRNA-146a and one SNP in ZBTB38-RASA2 with the disease susceptibility and the clinical features of the Chinese patients of sCJD and FFI.Immunochemical detection of prion protein on dipsticks prepared with crystalline bacterial cell-surface layers.Case of probable Creutzfeldt-Jakob disease presenting with complex partial seizure following sleeplessness and cognitive impairment.Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt-Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma.What psychiatrists should know about sporadic Creutzfeldt-Jakob disease.The EEG in E200K familial CJD: relation to MRI patterns.Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases
P2860
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P2860
Clinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests.
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Clinical diagnosis and differe ...... emphasis on laboratory tests.
@ast
Clinical diagnosis and differe ...... emphasis on laboratory tests.
@en
type
label
Clinical diagnosis and differe ...... emphasis on laboratory tests.
@ast
Clinical diagnosis and differe ...... emphasis on laboratory tests.
@en
prefLabel
Clinical diagnosis and differe ...... emphasis on laboratory tests.
@ast
Clinical diagnosis and differe ...... emphasis on laboratory tests.
@en
P2860
P1476
Clinical diagnosis and differe ...... emphasis on laboratory tests.
@en
P2093
Sigrid Poser
P2860
P356
10.1034/J.1600-0463.2002.100111.X
P577
2002-01-01T00:00:00Z