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Please use this identifier to cite or link to this item: https://repository.southwesthealthcare.com.au/swhealthcarejspui/handle/1/3566
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dc.contributor.authorZiukelis, Elina T.-
dc.contributor.authorSharma, Vasu Keshav-
dc.contributor.authorGome, James, J.-
dc.date.accessioned2023-03-17T04:57:33Z-
dc.date.available2023-03-17T04:57:33Z-
dc.date.issued2021-
dc.identifier.urihttps://repository.southwesthealthcare.com.au/swhealthcarejspui/handle/1/3566-
dc.description.abstractSporadic Creutzfeldt-Jakob disease should be considered in any case of rapid neuropsychiatric decline. While neuropathological examination of a brain biopsy specimen remains the only definitive diagnostic method and real-time quaking-induced conversion tests have simplified premortem diagnosis, careful evaluation of magnetic resonance imaging can provide readily accessible clues.-
dc.relation.isversionof20210723-
dc.subjectAcute Medicine-
dc.subjectGenetics-
dc.subjectGeriatric Medicine-
dc.subjectNeurology-
dc.subjectPsychiatry-
dc.titlePremortem diagnosis of pathologically confirmed sporadic Creutzfeldt-Jakob disease-
dc.typeJournal Article-
dc.identifier.journaltitleClinical Case Reports-
dc.accession.number34322245-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pubmed/34322245-
dc.description.affiliationSt Vincent's Health Australia Melbourne Vic Australia.-
dc.description.affiliationSouth West Healthcare Warrnambool Vic Australia.-
dc.description.affiliationHealth Imaging Services Warrnambool Vic Australia.-
dc.description.affiliationDeakin University Burwood Vic Australia.-
dc.format.startpagee04461-
dc.source.volume9-
local.issue.number7-
dc.identifier.noteseng-
dc.identifier.notesCase Reports-
dc.identifier.notesEngland-
dc.identifier.notes2021/07/30-
dc.identifier.notesClin Case Rep. 2021 Jul 23;9(7):e04461. doi: 10.1002/ccr3.4461. eCollection 2021 Jul.-
dc.identifier.importdoi10.1002/ccr3.4461-
dc.identifier.dateJul-
dc.identifier.dateNLM-
dc.contributor.swhauthorGome, James, J.-
dc.contributor.swhauthorSharma, Vasu Keshav-
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