Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
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Transmissible Spongiform Encephalopathies Affecting HumansUltra-sensitive detection of prion protein fibrils by flow cytometry in blood from cattle affected with bovine spongiform encephalopathyA proposal of new diagnostic pathway for fatal familial insomniaClinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests.Assessment of suspected dementia.Cerebrospinal fluid-optimized two-dimensional difference gel electrophoresis (2-D DIGE) facilitates the differential diagnosis of Creutzfeldt-Jakob disease.Sporadic Creutzfeldt-Jakob disease--a review.Prion diseases in man.Mad cow disease--the OR connection.Diagnosis of Creutzfeldt-Jakob disease by measurement of S100 protein in serum: prospective case-control studyClinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia.Unchanged survival rates of 14-3-3gamma knockout mice after inoculation with pathological prion protein.Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias.Gene expression profiling and association with prion-related lesions in the medulla oblongata of symptomatic natural scrapie animals.PrP immunohistochemistry: different protocols, including a procedure for long formalin fixation, and a proposed schematic classification for deposits in sporadic Creutzfeldt-Jakob disease.Creutzfeldt-Jakob disease and the eye. I. Background and patient management.Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.De novo prions.Altered Prion protein expression pattern in CSF as a biomarker for Creutzfeldt-Jakob disease.White matter involvement in sporadic Creutzfeldt-Jakob disease.Radiological assessment of Creutzfeldt-Jakob disease.Presenile dementia syndromes: an update on taxonomy and diagnosis.The Creutzfeldt-Jakob disease (CJD) neurological status scale: a new tool for evaluation of disease severity and progression.Pathologic evidence that the T188R mutation in PRNP is associated with prion disease.Patients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob diseaseCoexistence of CJD and Alzheimer's disease: an autopsy case showing typical clinical features of CJD.Creutzfeldt-Jakob disease in SwedenUltrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targetsIs Creutzfeldt-Jakob disease transmitted in blood?Correlating DWI MRI with pathologic and other features of Jakob-Creutzfeldt diseaseEthics in prion disease.Related or not? Development of spontaneous Creutzfeldt-Jakob disease in a patient with chronic, well-controlled HIV: A case report and review of the literatureRapidly progressive neurodegenerative dementias.Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation casesIdentification of differentially expressed genes in scrapie-infected mouse brains by using global gene expression technologyApplication of quantitative DTI metrics in sporadic CJD.Other dementias.Immunotherapeutic approaches in prion disease: progress, challenges and potential directions.When dementia progresses quickly: a practical approach to the diagnosis and management of rapidly progressive dementia.Incidence of Creutzfeldt-Jakob disease in Taiwan: a prospective 10-year surveillance.
P2860
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P2860
Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh-hant
name
Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@en
Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@nl
type
label
Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@en
Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@nl
prefLabel
Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@en
Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@nl
P2093
P1433
P1476
Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@en
P2093
H A Kretzschmar
J Tateishi
S J DeArmond
P304
P356
10.1001/ARCHNEUR.1996.00550090125018
P577
1996-09-01T00:00:00Z