ORCID "0000-0001-8893-1739" Makale Koleksiyonu için listeleme
-
Central areolar choroidal dystrophy case
Tanrıverdi, Cafer; Nurözler Tabakçı, Burcu; Şentürk, Fevzi (Gazi Eye Foundation, 2020)Central areolar choroidal dystrophy is a rarely seen, hereditary retinal disease which primarily affects macula. Here, we aimed to review clinical findings, ophthalmological imaging results and electrodiagnostic test results ... -
Comparison of biomicroscopy and light microscopy findings in demodex diagnosis in patients with chronic blepharitis
Tanrıverdi, Cafer; Balcı, Özlem; Demirci, Göktuğ; Odabaşı, Mahmut; Özsütçü, Mustafa; Nurözler Tabakçı, Burcu (Wolters Kluwer, 2020)OBJECTIVES: We aimed to compare the results of biomicroscopic examination and light microscopy in the diagnosis of Demodex infestation in chronic blepharitis cases. METHODS: The study was performed with retrospective data ... -
Evaluation of tear film layer and meibomian gland morphology in geriatric patients with chronic blepharitis
Tanrıverdi, Cafer; Nurözler Tabakçı, Burcu (Geriatrics Society, 2019)Introduction: To investigate the changes in meibomian gland morphology and their effects on tear parameters in geriatric patients with chronic blepharitis. Materials and Method: The study included 70 eyes of 35 healthy ... -
Multiple evanescent white dot syndrome presenting that as central serous chorioretinopathy
A 28-year-old man presented to the clinic with metamorphopsia, central scotoma, and visual loss in his right eye. After detailed ophthalmicexamination, fundoscopy showed localized elevation of the macula,and optical coherence ...