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dc.contributor.authorKocamış, Özkan
dc.contributor.authorÖrnek, Kemal
dc.contributor.authorTemel, Emine
dc.date.accessioned2022-12-28T06:51:16Z
dc.date.available2022-12-28T06:51:16Z
dc.date.issued2022en_US
dc.identifier.citationKocamış, Ö., Örnek, K., & Temel, E. (2022). Chiari I malformation presenting with ganglion cell complex thinning on routine examination. Arquivos Brasileiros de Oftalmologia, 85, 435-436.en_US
dc.identifier.issn00042749
dc.identifier.urihttps://doi.org/10.5935/0004-2749.2022-0150
dc.identifier.urihttps://hdl.handle.net/20.500.12513/4860
dc.description.abstractChiari I malformation (CMI) is a rare congenital disorder characterized by the caudal displacement of cerebellar tonsils through the foramen magnum into the cervical canal(1). Ophthalmological signs include retro-orbital pain, diplopia, photophobia, impaired visual acuity, nystagmus, strabismus, and papilledema(2-4). The diagnosis is mostly based on magnetic resonance imaging (MRI) findings © This content is licensed under a Creative Commons Attributions 4.0 International License.en_US
dc.language.isoengen_US
dc.publisherConselho Brasileiro De Oftalmologiaen_US
dc.relation.isversionof10.5935/0004-2749.2022-0150en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleChiari I malformation presenting with ganglion cell complex thinning on routine examinationen_US
dc.typeletteren_US
dc.relation.journalArquivos Brasileiros de Oftalmologiaen_US
dc.contributor.departmentTıp Fakültesien_US
dc.contributor.authorIDÖzkan Kocamış / 000000030353457Xen_US
dc.contributor.authorIDKemal Örnek / 0000-0002-7745-1892en_US
dc.contributor.authorIDEmine Temel / 0000-0001-6302-9175en_US
dc.identifier.volume85en_US
dc.identifier.issue4en_US
dc.identifier.startpage435en_US
dc.identifier.endpage436en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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