Atypical Sporadic Creutzfeldt-Jakob Disease Mimicking Nonconvulsive Status Epilepticus

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dc.contributor.authorUca, Ali Ulvi
dc.contributor.authorGenc, Bulent Oguz
dc.contributor.authorGuney, Figen
dc.contributor.authorAkpinar, Zehra
dc.date.accessioned2024-02-23T14:41:35Z
dc.date.available2024-02-23T14:41:35Z
dc.date.issued2014
dc.departmentNEÜen_US
dc.description.abstractSporadic Creutzfeldt- Jakob disease (sCJD) is the most common disorder among the very rare prion diseases (human transmissible subacute spongiform encephalopathies). The diagnosis might be easy if a patient with characteristics features of myoclonus, progressive dementia and periodic electroencephalography activity. Diagnosis of some patients with unusual symptoms and signs may be challenging. The reported case is a 65 years old female patient who was finally diagnosed as CJD, after previously being misdiagnosed with depression, dementia and refractory nonconvulsive status epilepticus.en_US
dc.identifier.doi10.5505/epilepsi.2014.86158
dc.identifier.endpage92en_US
dc.identifier.issn1300-7157
dc.identifier.issue2en_US
dc.identifier.startpage87en_US
dc.identifier.urihttps://doi.org/10.5505/epilepsi.2014.86158
dc.identifier.urihttps://hdl.handle.net/20.500.12452/16914
dc.identifier.volume20en_US
dc.identifier.wosWOS:000408851900007en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isotren_US
dc.publisherKare Publen_US
dc.relation.ispartofEpilepsien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCreutzfeldt-Jakob Diseaseen_US
dc.subjectNonconvulsive Status Epilepticusen_US
dc.subjectPrion Diseaseen_US
dc.titleAtypical Sporadic Creutzfeldt-Jakob Disease Mimicking Nonconvulsive Status Epilepticusen_US
dc.typeArticleen_US

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