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dc.contributor.authorŞengül A.
dc.contributor.authorArtunay Ö.
dc.contributor.authorTürkseven Kumral E.
dc.contributor.authorRasier R.
dc.contributor.authorErçalik Y.
dc.contributor.authorTükenmez Dikmen N.
dc.contributor.authorSevim Ş.
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T15:53:12Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T15:53:12Z
dc.date.issued2014
dc.identifier.issn1300-1256
dc.identifier.urihttp://hdl.handle.net/11446/1859
dc.description.abstractA 15-year-old male patient presented to our clinic with loss of central vision that began about 2 weeks before presentation. He diagnosed with hereditary maculopathy in another clinic. His visual acuity was 2/10. After he underwent FFA, OKT and multifocal ERG, he diagnosed as unilateral acute idiopathic maculopathy. His visual acuity recovered to 10/10 by the end of 5 weeks.en_US
dc.language.isoturen_US
dc.publisherGazi Eye Foundationen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHereditaryen_US
dc.subjectIdiopathicen_US
dc.subjectMaculopathyen_US
dc.subjectUnilateralen_US
dc.titleAn unilateral acute idiopathic maculopathy case: Masquerading as hereditary maculopathy [Herediter makülopati ile karişan unilateral akut idiyopatik makülopati olgusu]en_US
dc.typearticleen_US
dc.relation.journalRetina-Vitreusen_US
dc.departmentDBÜen_US
dc.identifier.issue4en_US
dc.identifier.volume22en_US
dc.identifier.startpage305en_US
dc.identifier.endpage307en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempDBÜen_US


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