Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
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Plasma and Cerebrospinal fluid (CSF) Abeta42 for the differential diagnosis of Alzheimer's disease dementia in participants diagnosed with any dementia subtype in a specialist care settingBiomarkers for sporadic Creutzfeldt-Jakob diseaseOlfactory Receptors in Non-Chemosensory Organs: The Nervous System in Health and DiseaseCreutzfeldt-Jakob Disease Presenting With Dizziness and Gaze-Evoked Nystagmus: A Case Report.Prion DiseasesThe use of cerebrospinal fluid and neuropathologic studies in neuropsychiatry practice and researchRacial and ethnic differences in individuals with sporadic Creutzfeldt-jakob disease in the United States of AmericaA study of clinical profile, radiological and electroencephalographic characteristics of suspected Creutzfeldt-Jakob disease in a tertiary care centre in South IndiaA proposal of new diagnostic pathway for fatal familial insomniaRole of magnetic resonance imaging, cerebrospinal fluid, and electroencephalogram in diagnosis of sporadic Creutzfeldt-Jakob disease.MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob diseaseDifferential diagnosis of Jakob-Creutzfeldt diseaseAnalyses of the survival time and the influencing factors of chinese patients with prion diseases based on the surveillance data from 2008-2011.Thalamic lesions: a radiological review.Cortical abnormalities on MRI: what a neurologist should know.Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease.Neuroradiology of human prion diseases, diagnosis and differential diagnosis.Interpretation of cerebrospinal fluid protein tests in the diagnosis of sporadic Creutzfeldt-Jakob disease: an evidence-based approach.Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias.An update on the diagnosis and management of dementing conditionsTreatable neurological disorders misdiagnosed as Creutzfeldt-Jakob diseaseThe epidemiological, clinical, and laboratory features of sporadic Creutzfeldt-Jakob disease patients in China: surveillance data from 2006 to 2010Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study.Can mortality data provide reliable indicators for Creutzfeldt-Jakob disease surveillance? A study in France from 2000 to 2008.Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.Population screening for variant Creutzfeldt-Jakob disease using a novel blood test: diagnostic accuracy and feasibility study.Gerstmann-Sträussler-Scheinker syndrome with the P102L pathogenic mutation presenting as familial Creutzfeldt-Jakob disease: a case report and review of the literature.Symptomatic aggravation after corticosteroid pulse therapy in definite sporadic Creutzfeldt-Jakob disease with the feature of Hashimoto's encephalopathy.Ascertainment bias causes false signal of anticipation in genetic prion diseaseA test for Creutzfeldt-Jakob disease using nasal brushings.Unusual deterioration in a patient with multiple sclerosis on natalizumab therapyImmune responses in rapidly progressive dementia: a comparative study of neuroinflammatory markers in Creutzfeldt-Jakob disease, Alzheimer's disease and multiple sclerosisWhite matter involvement in sporadic Creutzfeldt-Jakob disease.Chinese specific characteristics of sporadic Creutzfeldt-Jakob disease: a retrospective analysis of 57 cases.Magnetic resonance imaging findings in probable Creutzfeld-Jacob disease: comparison with electroencephalography and cerebrospinal fluid characteristics.Mathematical models for the diffusion magnetic resonance signal abnormality in patients with prion diseases.Detection of the GPI-anchorless prion protein fragment PrP226* in human brain.Characteristic CSF prion seeding efficiency in humans with prion diseasesInvestigating the association of ApoE genotypes with blood-brain barrier dysfunction measured by cerebrospinal fluid-serum albumin ratio in a cohort of patients with different types of dementiaDiagnostic profiles of patients with late-onset Creutzfeldt-Jakob disease differ from those of younger Creutzfeldt-Jakob patients: a historical cohort study using data from the German National Reference Center.
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Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
description
article científic
@ca
article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
@tr
scientific article published on 22 September 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@en
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@nl
type
label
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@en
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@nl
prefLabel
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@en
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@nl
P2093
P2860
P50
P356
P1433
P1476
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
@en
P2093
A Ladogana
A Taratuto
B Meissner
D M Summers
G B Stokin
Gerard H Jansen
P2860
P304
P356
10.1093/BRAIN/AWP191
P407
P577
2009-09-22T00:00:00Z