about
Neuroimaging biomarkers of neurodegenerative diseases and dementiaPeripheral prion pursuitUse of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob diseaseDura mater-associated Creutzfeldt-Jakob disease: experience from surveillance in the UK.Clinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests.Human transmissible spongiform encephalopathies in eleven countries: diagnostic pattern across time, 1993-2002.PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States.First hundred cases of variant Creutzfeldt-Jakob disease: retrospective case note review of early psychiatric and neurological features.Variant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public healthNew variant Creutzfeldt-Jakob disease: the epidemic that never wasVariant CJD. 18 years of research and surveillance.Variant Creutzfeldt-Jakob disease: risk of transmission by blood transfusion and blood therapies.Possible underascertainment of variant Creutzfeldt-Jakob disease: a systematic studyCreutzfeldt-Jakob disease: implications for gastroenterology.Presenile dementia syndromes: an update on taxonomy and diagnosis.Prion diseases: epidemiology in man.Variant Creutzfeldt-Jakob disease: an unfolding epidemic of misfolded proteins.Adaptation of the bovine spongiform encephalopathy agent to primates and comparison with Creutzfeldt-- Jakob disease: implications for human healthPeripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study.Variant Creutzfeldt-Jakob disease and its transmission by blood.Ethical considerations in presymptomatic testing for variant CJD.The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease.Distinct neuropsychological characteristics in Creutzfeldt-Jakob disease.Comparative Incidence of Conformational, Neurodegenerative Disorders.Creutzfeldt-Jakob Disease in a Tertiary Care Hospital in Thailand: A Case Series and Review of the LiteratureIdentification of multiple quantitative trait loci linked to prion disease incubation period in mice.Neurological disorders presenting mainly in adolescenceRaised CSF phospho-tau concentrations in variant Creutzfeldt-Jakob disease: diagnostic and pathological implications.Neuroimaging findings in human prion disease.Genetic and environmental factors modify bovine spongiform encephalopathy incubation period in mice.Etiologic Framework for the Study of Neurodegenerative Disorders as Well as Vascular and Metabolic Comorbidities on the Grounds of Shared Epidemiologic and Biologic FeaturesEpidemiology of early-onset dementia: a review of the literature.Characterization of variant Creutzfeldt-Jakob disease prions in prion protein-humanized mice carrying distinct codon 129 genotypes.Clinicopathologic characteristics of five autopsied cases of dura mater-associated Creutzfeldt-Jakob disease.Drivers: A Biologically Contextualized, Cross-Inferential View of the Epidemiology of Neurodegenerative Disorders.Detection of proteinase K resistant proteins in the urine of patients with Creutzfeldt-Jakob and other neurodegenerative diseasesEthics in prion disease.Protective Effect of Val129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease.Rapidly progressive dementia.
P2860
Q27691820-48574C8B-987D-4B43-BD49-BE51D0572683Q28349664-10CC5148-DC00-436D-BA48-60D7412A9498Q28366081-368B1BDA-3AE5-49EF-94DC-13855713F61BQ30488585-44F1018D-D163-42A1-8498-A35D5A997A31Q30698122-29DA3F4E-F0E6-458B-B51F-CDC22C970116Q33263263-2B44ACED-54B0-431A-A377-EDEF231383C4Q33520832-1FD67DDE-EA43-40C7-A8DE-1D5F21453E45Q33526357-DECE6E53-F52D-4D0E-AEAD-C1379A6F33D8Q33875443-EB4ECE12-3108-477B-84A2-4DD69B6EB462Q33956087-346EFE61-3586-4987-A8F9-20FEA8736981Q34399623-2B3365B0-FFBE-4D81-AB65-5797C70A74E8Q34453109-D9B16871-BD99-42BF-8802-8251E0C4B2C0Q34489473-8F05416D-C2BB-40CF-9650-5C3F97835688Q34542333-A6691E00-3CE0-433A-A137-C9B73D9D9685Q34637604-7FA6AEB4-48C3-4F8D-BD36-323004A8F48FQ34649249-CA182A96-F0B7-45A5-9EA7-F1E9740F419DQ34685431-64FE4690-BE2D-43D5-88E3-9CB3E61F75F3Q34986039-328B91B2-44FF-4556-9C10-EED9B40A611FQ35057650-BBC85A21-FD59-4430-8FB5-B2D665698945Q35083260-19C34002-0F42-4C46-99C8-A656BEB07057Q35181622-1A3F1225-B548-41C2-B772-54A86CFDB3E0Q35428275-98F55DED-2A05-4D06-ABE7-0F216C0C9F62Q35486440-8983357E-D470-4D9F-A7E3-0445CDF6E516Q35560107-872CCE3B-C427-4783-8EC4-E155EEE74CEDQ35763399-146CF851-BCD2-4DF8-999C-3713AA6D9F1EQ35790077-764F0990-EEB2-494D-87DE-D07D3F66B60EQ35939147-1E708FD1-7542-4962-B798-D399A9438B6BQ36154356-94980325-8627-479A-B8EE-D09B64A0CDAFQ36226169-1041F76F-E76A-4AAF-B3F1-E8B1F627AF5CQ36226989-674079A6-474A-4C34-B2CE-D29A952DB430Q36308139-70D186CB-F0A9-4CA8-9C32-C48A805A7C5AQ36995708-582DFD6D-6EAF-413D-BD15-394353C6D3E3Q37025574-117CC170-D48F-4245-88A9-EF8A3D308CA7Q37048362-16D0EC4D-1958-427D-B97D-2520AEF57A9BQ37053085-79FFD028-0151-4600-9103-AF994A431FF3Q37053839-F5DB22F6-8943-4054-AC94-BDCB1B23FCBAQ37135774-9E8269A9-6E13-4BB2-A177-42791DD93AC8Q37282279-F3023B52-AD56-447E-824C-D0DF443677A5Q41530801-14208F54-5DB3-47E3-B215-497B60983C98Q42034203-0CBEBAAD-41F2-4DFE-A72B-C5F9F20752AE
P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի մայիսին 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
Diagnosis of new variant Creutzfeldt-Jakob disease.
@ast
Diagnosis of new variant Creutzfeldt-Jakob disease.
@en
Diagnosis of new variant Creutzfeldt-Jakob disease.
@nl
type
label
Diagnosis of new variant Creutzfeldt-Jakob disease.
@ast
Diagnosis of new variant Creutzfeldt-Jakob disease.
@en
Diagnosis of new variant Creutzfeldt-Jakob disease.
@nl
prefLabel
Diagnosis of new variant Creutzfeldt-Jakob disease.
@ast
Diagnosis of new variant Creutzfeldt-Jakob disease.
@en
Diagnosis of new variant Creutzfeldt-Jakob disease.
@nl
P2093
P1433
P1476
Diagnosis of new variant Creutzfeldt-Jakob disease.
@en
P2093
G E Stewart
J Mackenzie
K Estibeiro
M A Macleod
R S Knight
S N Cousens
P304
P356
10.1002/1531-8249(200005)47:5<575::AID-ANA4>3.3.CO;2-N
P577
2000-05-01T00:00:00Z