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dc.contributor.authorKeohane, C
dc.date.accessioned2012-02-03T15:12:51Z
dc.date.available2012-02-03T15:12:51Z
dc.date.issued2012-02-03T15:12:51Z
dc.identifier.citationLancet. 2000 Apr 22;355(9213):1384.en_GB
dc.identifier.issn0140-6736 (Print)en_GB
dc.identifier.issn0140-6736 (Linking)en_GB
dc.identifier.pmid10791518en_GB
dc.identifier.doi10.1016/S0140-6736(00)02133-4en_GB
dc.identifier.urihttp://hdl.handle.net/10147/209122
dc.language.isoengen_GB
dc.subject.meshBias (Epidemiology)en_GB
dc.subject.meshCreutzfeldt-Jakob Syndrome/classification/*pathologyen_GB
dc.subject.meshDiagnosis, Differentialen_GB
dc.subject.meshHumansen_GB
dc.subject.mesh*Magnetic Resonance Imagingen_GB
dc.subject.meshReproducibility of Resultsen_GB
dc.subject.meshSensitivity and Specificityen_GB
dc.subject.meshSeverity of Illness Indexen_GB
dc.subject.meshThalamic Nuclei/*pathologyen_GB
dc.titlePulvinar sign on MRI images in variant Creutzfeldt-Jakob disease.en_GB
dc.contributor.departmentHistopathology Department, Cork University Hospital, Wilton, Ireland.en_GB
dc.identifier.journalLanceten_GB
dc.description.provinceMunster


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