Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Gamze Men"'
Autor:
Esra Arun Özer, Özlem Sivaslı Gül, Gamze Men, Ekrem Talay, Sümer Sütçüoğlu, Ali Kanık, Ebru Türkoğlu, Zelal Kahramaner, Hese Coşar, Aydın Erdemir, Işın Yaprak
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 41, Iss 5, Pp 309-313 (2011)
Pur po se: Retinopathy of prematurity (ROP) is a proliferative vascular disease which affects premature newborns and occurs during vessel development. The pathogenesis of ROP is complex and includes oxidative damage to the developing retina. The aim
Externí odkaz:
https://doaj.org/article/fe2069ac509e4107ae15e7a3cc9f8809
Autor:
Özlem Gül Sivasli, Sümer Sütçüoğlu, Gamze Men, Isin Yaprak, Esra Özer Arun, Ebru Türkoğlu, Hese Cosar, Ekrem Talay, Aydin Erdemir, Muhammet Ali Kanik, Zelal Kahramaner
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 41, Iss 5, Pp 309-313 (2011)
Pur po se: Retinopathy of prematurity (ROP) is a proliferative vascular disease which affects premature newborns and occurs during vessel development. The pathogenesis of ROP is complex and includes oxidative damage to the developing retina. The aim
Autor:
Esra Arun Ozer, Aydin Erdemir, Isin Yaprak, Sumer Sutcuoglu, Hese Cosar, Gamze Men, Zelal Kahramaner, Ebru Turkoglu, Tansu Ballı, Ali Kanik
Publikováno v:
Volume: 46, Issue: 1 1-5
Türk Pediatri Arşivi
Türk Pediatri Arşivi
Amaç: Günümüzde yard›mc› üreme tekniklerinin (YÜT) kullan›m›n›n artmas› ile birlikte, bu gebeliklere ba¤l› erken do¤um ve ço¤ul gebelik oranlar› da artm›flt›r. Bu çal›flmada, klini¤imizde YÜT ile sa¤lanan gebelikle
Publikováno v:
Journal of Pediatric Ophthalmology & Strabismus. 47:1-4
Three cases of Usher syndrome associated with a variant of Dandy–Walker malformation in three siblings from consanguineous Turkish parents are described. The siblings had retinitis pigmentosa and hearing loss. Two of the siblings also had mental re
Publikováno v:
The Journal of Tepecik Education and Research Hospital. 18:134-139
Publikováno v:
Clinical and Experimental Optometry. 90:367-370
Purpose: To report a case of Alport’s syndrome and to present electronmicroscopic examination findings of the anterior lens capsule of this patient. Method: A 21-year-old man was referred for low visual acuity and retinal pigment epithelial changes
Publikováno v:
Neuro-Ophthalmology. 29:9-15
Purpose: To present detailed clinical findings of a Turkish family from central Anatolia with a hereditary form of optic atrophy. Design: Observational case series. Material and methods: A detailed family history of a patient with optic atrophy revea
Autor:
Christina Canakis, Mandi D Conway, Ramakrishna Ratnakaram, Georges Naaman, Gholam A. Peyman, Gamze Men, Charalampos Livir-Rallatos
Publikováno v:
Ophthalmic Surgery, Lasers and Imaging Retina. 35:168-171
Two consecutive patients with idiopathic central serous chorioretinopathy and decreased vision subsequent to subfoveal choroidal neovascular membranes were treated with photodynamic therapy applied using the protocol of the Treatment of AgeRelated Ma
Publikováno v:
Neuro-Ophthalmology. 28:13-21
Objective: To discuss different combinations of headache, pseudopapilledema (due to optic nerve head drusen), and pseudotumor cerebri (PTC). Materials and methods: We present two case reports with ...
Publikováno v:
Lasers in Surgery and Medicine. 35:157-162
Background and Objective To study the effect of indocyanine green (ICG) pretreatment on threshold parameters of transscleral diode laser thermotherapy-induced threshold coagulation of the ciliary body. The procedure was termed ‘cyclothermotherapy