Ara
Toplam kayıt 5, listelenen: 1-5
The levels of IL-8 and TNF-A in vitreous samples from patients with diabetic retinopathy [Diabetik Retinopatili Hastalarín Vitreus Örneklerinde IL-8 ve TNF-A Seviyeleri]
(2011)
Purpose: Diabetic retinopathy (DR) is a frequent microvascular complication which is leading to sudden and severe loss in visual acuity in diabetes mellitus (DM) patients. Purpose is to compare the vitreous sample levels ...
An unilateral acute idiopathic maculopathy case: Masquerading as hereditary maculopathy [Herediter makülopati ile karişan unilateral akut idiyopatik makülopati olgusu]
(Gazi Eye Foundation, 2014)
A 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 ...
Results of intravitreal ranibizumab treatment for choroidal neovascularization secondary to age-related macular degeneration [Yaşa ba?li maküla dejenerasyonuna i?kincil gelişen koroid neovaskülarizasyonlarinda i?ntravitreal ranibizumab tedavi sonuçlarimiz]
(2010)
Purpose: To report the efficacy and results of intravitreal ranibizumab (IVR) injection for choroidal neovascularization due to age-related macular degeneration (ARMD). Materials and Methods: Fifty-eight eyes of 43 ARMD ...
Dexamethasone intravitreal implant in patients with macular edema due to retinal vein occlusion: 6 months results [Retina ven dal tıkanıklarının tedavisinde kullanılan tek doz intravitreal deksametazon implant Uygulamalarımızın 6 Aylık Sonuçları]
(Gazi Eye Foundation, 2015)
Purpose: To determine 6-month results after a single application of dexamethasone intravitreal implant (IVD) used in macular edema (ME) following branch retinal vein occlusion (BRVO). Materials and Methods: The findings ...
Association between Stargardt's disease and Retinitis Pigmentosa: Is common genetic mutation responsible? [Stargardt hastali?i ve Retinitis Pigmentosa birlikteli?i: Ortak genetik mutasyon mu sorumlu?]
(2011)
In this study the association between Stargardt's disease (STGD) and Retinisitis Pigmentosa (RP), both of which is seen in a case with a mutated ABCA4 gene, is analysed. Fundus exaimination was performed to a 23 years old ...