Yazar "Özdemir, Özdemir" için listeleme
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Anatomical and visual outcomes of ranibizumab injections in retinal pigment epithelium tears
Erol, Muhammet Kazım; Özdemir, Özdemir; Çoban, Deniz Turgut; Ceran, Başak Bostancı; Sarı, Esin Sögütlü (Consel Brasil Oftalmologia, 2015)Purpose: To report the anatomical and visual results in patients diagnosed as having retinal pigment epithelium (RPE) tears after receiving ranibizumab injections. Methods: Eyes diagnosed as having RPE tears with a minimum ... -
Comparison of intravitreal ranibizumab and bevacizumab treatment for retinopathy of prematurity
Erol, Muhammet Kazım; Çoban, Deniz Turgut; Sarı, Esin Söğütlü; Bilgin, Ahmet Burak; Doğan, Berna; Özdemir, Özdemir; Tunay, Zuhal Özen (Consel Brasil Oftalmologia, 2015)Purpose: To compare the efficacy of intravitreal ranibizumab and bevacizumab treatment for type 1 retinopathy of prematurity (ROP). Methods: 36 eyes of 20 patients with type 1 ROP who received anti-vascular endothelial ... -
Macular findings obtained by spectral domain optical coherence tomography in retinopathy of prematurity
Erol, Muhammet Kazım; Özdemir, Özdemir; Çoban, Deniz Turgut; Bilgin, Ahmet Burak; Doğan, Berna; Sarı, Esin Söğütlü (Hindawi Publishing Corporation, 2014)Purpose. To examine the macular findings obtained with spectral domain optical coherence tomography (SD OCT) in infants with retinopathy of prematurity (ROP). Materials and Methods. The macular SD OCT images of 190 premature ... -
A novel mutation of SGK1 gene in central serous chorioretinopathy
Akyol, Mahmut; Erol, Muhammet Kazım; Özdemir, Özdemir; Çoban, Deniz Turgut; Bilgin, Ahmet Burak; Sarı, Esin Sögütlü; Türkoğlu, Elif Betül (IJO Press, 2015)AIM: To investigate the association of serum glucocorticoid kinase gene-1 (SGK-1) DNA variants with chronic central serous chorioretinopathy (CSC). METHODS: We enrolled 32 eyes of 32 patients who were diagnosed with ... -
Peripheral facial paralysis in a newborn with charge syndrome
CHARGE Syndrome is a genetic disorder that affects many organs. Approximately two-thirds of the cases have CHD7 mutations. Most individuals with this syndrome have a coloboma in their eyes. Coloboma can be found in one or ...
