Ara
Toplam kayıt 7, listelenen: 1-7
Association between Stargardt's disease and Retinitis Pigmentosa: Is common genetic mutation responsible? [Stargardt hastaliği ve Retinitis Pigmentosa birlikteliği: 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 ...
Results of intravitreal ranibizumab treatment for choroidal neovascularization secondary to age-related macular degeneration [Yaşa bağli 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 ...
The levels of IL-8 and TNF-A in vitreous samples from patients with diabetic retinopathy
(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 ...
Results of intravitreal ranibizumab treatment for choroidal neovascularization secondary to age-related macular degeneration
(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
(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?
(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 ...
An unilateral acute idiopathic maculopathy case: Masquerading as hereditary maculopathy
(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 ...