Diffusion MR Imaging in Sporadic Creutzfeldt-Jakob Disease

dc.contributor.authorPekoz, Burcak Cakir
dc.contributor.authorAlkan, Ozlem
dc.contributor.authorGiray, Semih
dc.contributor.authorDemir, Senay
dc.contributor.authorAltinkaya, Naime
dc.contributor.orcID0000-0001-7526-3460en_US
dc.contributor.orcID0000-0003-1348-8167en_US
dc.contributor.orcID0000-0002-4209-9075en_US
dc.contributor.orcID0000-0002-0722-3181en_US
dc.contributor.researcherIDAAM-4169-2021en_US
dc.contributor.researcherIDAAM-5169-2021en_US
dc.contributor.researcherIDAAK-9310-2021en_US
dc.contributor.researcherIDAAH-1091-2020en_US
dc.date.accessioned2024-03-19T12:25:09Z
dc.date.available2024-03-19T12:25:09Z
dc.date.issued2014
dc.description.abstractCreutzfeldt-Jakob disease (CJD) is a rare dementing disease and is thought to caused by a prion. It is characterized by rapidly progressive dementia, ataxia, myoclonus, akineticmutism and eventual death. Brain biopsy or autopsy is required for a definitive diagnosis of CJD. Diffusion-weighted imaging became an important tool for early diagnosis of CJD because of the high sensitivity. We present 59-year-old female patient diagnosed as sporadic CJD with typical MR imagings.en_US
dc.identifier.eissn2602-3040en_US
dc.identifier.endpage883en_US
dc.identifier.issn2602-3032en_US
dc.identifier.issue4en_US
dc.identifier.startpage880en_US
dc.identifier.urihttp://hdl.handle.net/11727/11879
dc.identifier.volume39en_US
dc.identifier.wos000216471400028en_US
dc.language.isoturen_US
dc.relation.journalCUKUROVA MEDICAL JOURNALen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBasal gangliaen_US
dc.subjectCreutzfeldt-Jakob diseaseen_US
dc.subjectDiffusion MR imagingen_US
dc.titleDiffusion MR Imaging in Sporadic Creutzfeldt-Jakob Diseaseen_US
dc.typearticleen_US

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