Diffusion MR Imaging in Sporadic Creutzfeldt-Jakob Disease
dc.contributor.author | Pekoz, Burcak Cakir | |
dc.contributor.author | Alkan, Ozlem | |
dc.contributor.author | Giray, Semih | |
dc.contributor.author | Demir, Senay | |
dc.contributor.author | Altinkaya, Naime | |
dc.contributor.orcID | 0000-0001-7526-3460 | en_US |
dc.contributor.orcID | 0000-0003-1348-8167 | en_US |
dc.contributor.orcID | 0000-0002-4209-9075 | en_US |
dc.contributor.orcID | 0000-0002-0722-3181 | en_US |
dc.contributor.researcherID | AAM-4169-2021 | en_US |
dc.contributor.researcherID | AAM-5169-2021 | en_US |
dc.contributor.researcherID | AAK-9310-2021 | en_US |
dc.contributor.researcherID | AAH-1091-2020 | en_US |
dc.date.accessioned | 2024-03-19T12:25:09Z | |
dc.date.available | 2024-03-19T12:25:09Z | |
dc.date.issued | 2014 | |
dc.description.abstract | Creutzfeldt-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.eissn | 2602-3040 | en_US |
dc.identifier.endpage | 883 | en_US |
dc.identifier.issn | 2602-3032 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.startpage | 880 | en_US |
dc.identifier.uri | http://hdl.handle.net/11727/11879 | |
dc.identifier.volume | 39 | en_US |
dc.identifier.wos | 000216471400028 | en_US |
dc.language.iso | tur | en_US |
dc.relation.journal | CUKUROVA MEDICAL JOURNAL | en_US |
dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Basal ganglia | en_US |
dc.subject | Creutzfeldt-Jakob disease | en_US |
dc.subject | Diffusion MR imaging | en_US |
dc.title | Diffusion MR Imaging in Sporadic Creutzfeldt-Jakob Disease | en_US |
dc.type | article | en_US |
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