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Assessment of serum levels of angiogenic factors in dizygotic twin infants with and without retinopathy of prematurity
Demir S.; Ortak H.; Aygün C.; Yücel Ö.E.; Arslanbek M.E.; Küçüködük Ş.; Beden Ü. (Ondokuz Mayis Universitesi, 2013)The aim of the study was to evaluate the plasma concentrations of vascular endothelial growth factor (VEGF-A), its soluble receptors VEGFR-1 and VEGFR-2, insulin like growth factor (IGF-1) and soluble Tie-2 in twin infants ... -
Combined phacoemulsification and pars plana vitrectomy in diabetic patients
Süllü Y.; Beden Ü.; UluGüngör I.; Hamidova R. (2006)Background: To evaluate combined phacoemulsification, foldable acrylic intraocular lens (IOL) implantation and pars plana vitrectomy (PPV) in diabetic patients with vitreoretinal pathology. Methods: Combined surgery was ... -
Combined phacoemulsification and silicone oil removal with assistance of anterior chamber maintainer
Süllü Y.; Beden Ü.; Hamidova R.; Alotaby H. (2006)Background: To evaluate the using of anterior chamber maintainer (ACM) in combined phacoemulsification and silicone oil removal through posterior capsulorhexis in silicone oil filled eyes. Methods: Combined cataract ... -
Morbidity and mortality of very low birth weight infants followed in neonatal intensive care unit
Çakmak Çelik F.; Aygün C.; Tanyeri B.; Beden Ü.; Küçüködük Ş.; Çetinoğlu E.; Aksakal E. (2007)In recent years survival of very low birth weight (VLBW) infants has increased by the technical and scientific developments in neonatology. However, chronic diseases like bronchopulmonary dysplasia (BPD), retinopathy of ... -
Ophthalmologic findings in a case of Sjögren-Larsson syndrome
Demir S.; Beden Ü.; Özarslan M.; Erkan D. (2009)Sjögren-Larsson syndrome (SLS) is a recessively inherited disorder characterized by congenital icthyosis, spastic diplegia and mental retardation. The disorder is caused by mutations in the aldehyde dehydrogenase family ... -
Pigmentary maculopathy in a patient with cystinosis
Cystinosis is a rare autosomal recessive lysosomal storage disorder. It is characterized by the intracellular accumulation of cystine. The gene for nephropathic cystinosis has been mapped to chromosome 17p13. Corneal and ... -
Regression of severe corneal stromal neovascularization with topical cyclosporine 0.05% after penetrating keratoplasty for fungal corneal ulcer
Purpose: To report regression of corneal stromal neovascularizations with the use of topical cyclosporine 0.05% in a corneal transplant patient performed for fungal corneal ulcer. Design Case report. Methods: A 14-year-old ...
