Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering.
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Transmissible Spongiform Encephalopathies Affecting HumansRapidly progressive dementia due to Mycobacterium neoaurum meningoencephalitisAssignment of the human and mouse prion protein genes to homologous chromosomesPrionsAkinetic mutism as a classification criterion for the diagnosis of Creutzfeldt-Jakob diseaseA brief history of prionsImplications for Creutzfeldt-Jakob disease (CJD) in dentistry: a review of current knowledge.A study of clinical profile, radiological and electroencephalographic characteristics of suspected Creutzfeldt-Jakob disease in a tertiary care centre in South IndiaDifferential diagnosis of Jakob-Creutzfeldt diseaseClinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests.Creutzfeldt-Jakob disease segregating in a three generation Danish family.Neurodegeneration in humans caused by prionsHeidenhain variant of Creutzfeldt-Jakob disease: An autopsy study from India.A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. I: Clinical featuresA retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-1979. II: Epidemiology.Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factors.Transmission of Creutzfeldt-Jakob disease to a chimpanzee by electrodes contaminated during neurosurgery.Creutzfeldt-Jakob disease in AustriaDiagnosis of Creutzfeldt-Jakob disease by measurement of S100 protein in serum: prospective case-control studyDietary Risk Factors for Sporadic Creutzfeldt-Jakob Disease: A Confirmatory Case-Control Study.Search for a prion-specific nucleic acid.PrP immunohistochemistry: different protocols, including a procedure for long formalin fixation, and a proposed schematic classification for deposits in sporadic Creutzfeldt-Jakob disease.Variant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public healthRisk of acquiring Creutzfeldt-Jakob disease from blood transfusions: systematic review of case-control studies.Creutzfeldt-Jakob disease and haemophilia: assessment of risk.Creutzfeldt-Jakob disease and the eye. I. Background and patient management.Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.Creutzfeldt-Jakob disease: the problem of recipient notification.Concurrent variably protease-sensitive prionopathy and amyotrophic lateral sclerosis.Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.Experimental transmission of an autosomal dominant spongiform encephalopathy: does the infectious agent originate in the human genome?The transmissible spongiform encephalopathies (prion diseases): a review for dental surgeons.Slow viruses and chronic disease: the contribution of epidemiologyTransmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP geneHashimoto's encephalitis as a differential diagnosis of Creutzfeldt-Jakob diseasePatients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob diseaseA prospective study of CSF markers in 250 patients with possible Creutzfeldt-Jakob disease.Distinct neuropsychological characteristics in Creutzfeldt-Jakob disease.Transmission of scrapie prions to primate after an extended silent incubation period.From slow virus to prion: a review of transmissible spongiform encephalopathies.
P2860
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P2860
Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering.
description
1979 nî lūn-bûn
@nan
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
1979年论文
@zh
1979年论文
@zh-cn
name
Creutzfeldt-Jakob disease: pat ...... ilial and sporadic clustering.
@en
type
label
Creutzfeldt-Jakob disease: pat ...... ilial and sporadic clustering.
@en
prefLabel
Creutzfeldt-Jakob disease: pat ...... ilial and sporadic clustering.
@en
P2093
P356
P1433
P1476
Creutzfeldt-Jakob disease: pat ...... ilial and sporadic clustering.
@en
P2093
Bernoulli C
Gajdusek DC
Gibbs CJ Jr
Masters CL
P304
P356
10.1002/ANA.410050212
P577
1979-02-01T00:00:00Z