Search Results - "Altıntaş, Ayşegül"

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    Comparison of ocular response analyzer parameters in primary open angle glaucoma and exfoliative glaucoma patients by Beyazyildiz, Emrullah, Beyazyıldız, Özlem, Arifoğlu, Hasan, Altıntaş, Ayşegül, Köklü, Șükrü

    Published in Indian journal of ophthalmology (01-07-2014)
    “…Aim: We sought to identify differences in the following measures of the ocular response analyser (ORA) between primary open angle glaucoma (POAG) and…”
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    Journal Article
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    Toxic Anterior Segment Syndrome Outbreak after Cataract Surgery Triggered by Viscoelastic Substance by Altıntaş, AyşeGül Koçak, Ciritoğlu, Meryem Yaşar, BeyazyıldıZ, Özlem, Can, Çiğdem Ülkü, Polat, Sibel

    “…The purpose of this study is to present toxic anterior segment syndrome (TASS) outbreak at our clinic and discuss possible causes of TASS. Thirty-four eyes of…”
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    Journal Article
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    COVID-19 Pandemic and Ophthalmic Effect on Strabismus and Pediatric Eye Disorders by Ayşegül KOÇAK ALTINTAŞ

    “…An ongoing outbreak of pandemic caused by a novel coronavirus has severely infected humans worldwide. Even the characteristic symptom of COVID-19 is severe…”
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    The use of the QuantiFERON-tuberculosis gold test in the diagnosis of ocular tuberculosis by Ozdamar, Yasemin, Ozkan, Seyhan S, Beyazyildiz, Emrullah, Ozdal, Pinar Cakar, Teberik, Kuddusi, Altintas, Aysegul Kocak

    “…Ocular tuberculosis without systemic manifestations may rarely occur. The diagnosis of ocular tuberculosis is important because it has a wide spectrum of…”
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    Results of classical and augmented bimedial rectus recession in infantile esotropia by Altintas, Aysegül Koçak, Yilmaz, F. Gül, Duman, Sunay

    Published in Strabismus (1999)
    “…PURPOSE. To compare the success rates of augmented bimedial rectus recession and the standard recession. MATERIALS AND METHODS. Ninety patients were included…”
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    Human microphthalmia associated with mutations in the retinal homeobox gene CHX10 by Sarfarazi, Mansoor, McInnes, Roderick R, Ferda Percin, E, Ploder, Lynda A, Yu, Jessica J, Arici, Kemal, Jonathan Horsford, D, Rutherford, Adam, Bapat, Bharati, Cox, Diane W, Duncan, Alessandra M.V, Kalnins, Vitauts I, Kocak-Altintas, Aysegul, Sowden, Jane C, Traboulsi, Elias

    Published in Nature genetics (01-08-2000)
    “…Isolated human microphthalmia/anophthalmia, a cause of congenital blindness, is a clinically and genetically heterogeneous developmental disorder characterized…”
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    Anizometropik ambliyopisi olan hastalarda 'iyi gören göz' gerçekten sağlıklı mı? by ALTINTAŞ, Ayşegül K, ŞİMŞEK, Şaban, YÜLEK, Fatma, SİMAVLI, Hüseyin, DAL, Derya, ÇAKMAK, Hasan B

    Published in Türk Oftalmoloji Gazetesi (2009)
    “…Amaç: Ambliyop hastalarin ambliyop ve sağlam gözlerinin kontrast duyarlıklarının normal sağlıklı bireylerin kontrast duyarlıklarıyla karşılaştırılması. Yöntem:…”
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    Journal Article
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    Autosomal recessive nanophthalmos by Altintaş, Ayşegül Koçak, Acar, Mehmet Akif, Yalvaç, Ilgaz Saĝdiç, Koçak, Inci, Nurözler, Ayşe, Duman, Sunay

    Published in Acta ophthalmologica Scandinavica (01-06-1997)
    “…Nanophthalmos is a rare congenital ocular malformation which is generally recognized at middle age when serious complications have already developed. In this…”
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