Search Results - "Bingol Kiziltunc, Pinar"

Visual habilitation in young children with visual impairment by Sahli, Esra, Bingol Kiziltunc, Pinar, Idil, Aysun

“…Purpose To evaluate the effectiveness of the visual habilitation programme in improving the visual functions of visually impaired children under 3 years old…”
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A novel biomarker for increased intracranial pressure in idiopathic intracranial hypertension by Bingöl Kızıltunç, Pınar, Atilla, Huban

“…Purpose Changes in optic disc and peripapillary structures associated with optic nerve edema in idiopathic intracranial hypertension (IIH), can be evaluated…”
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Ocular vascular changes during pregnancy: an optical coherence tomography angiography study by Kızıltunç, Pınar Bingöl, Varlı, Bulut, Büyüktepe, Tuna Çelik, Atilla, Huban

“…Background Pregnancy is a period presenting with many physiological adaptation mechanisms. One of the structures in which these mechanisms are observed is…”
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Ocular Findings of Pediatric Dry Eye Related to Graft-Versus-Host Disease by Kiziltunc, Pinar Bingol, Buyuktepe, Tuna Celik, Yalcindag, Fatime Nilufer, Ertem, Mehmet, Ince, Elif, Ileri, Talia, Atilla, Huban

“…Objectives: To evaluate the frequency and findings of dry eye associated with ocular graft-versus-host disease (GVHD) in pediatric hematopoietic stem cell…”
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Fundus Autofluorescence Changes in Age-related Maculopathy by Sermet, Figen, Kiziltunc, Pinar Bingol

“…The aim of this study was to describe the fundus autofluorescence (FAF) findings of age-related maculopathy and risk patterns associated with FAF changes. FAF…”
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Optical Coherence Tomography Angiography Findings in Long-Term Follow-up of Leber's Hereditary Optic Neuropathy: Report of Two Cases by Bingöl Kızıltunç, Pınar, Tüntaş Bilen, Feyza, Atilla, Huban

“…Leber's hereditary optic neuropathy (LHON) is thought to be a neurovascular disease due to presence of vascular changes in asymptomatic patients. Here we…”
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Bilaterally Diffuse Lacrimal Gland Involvement: Initial Presentation of Systemic Sarcoidosis by Bingöl Kızıltunç, Pınar, Çiftçi, Fatma, Hoşal, Banu, Kaygusuz, Gülşah

“…Orbital involvement in systemic sarcoidosis is a rare condition. We report a case of orbital sarcoidosis with bilaterally huge lacrimal gland involvement as…”
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Results of Screening in Schools for Visually Impaired Children by Bingöl Kızıltunç, Pınar, İdil, Aysun, Atilla, Hüban, Topalkara, Ayşen, Alay, Cem

“…The aim of this study was to identify the causes of visual impairment in children attending schools for students with visual impairment and to identify…”
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Vascular changes with optical coherence tomography angiography during aura of migraine: A case report by Bingöl Kızıltunç, Pınar, Atilla, Huban

“…Purpose: To demonstrate macular and optic disk vessel changes by optical coherence tomography angiography during and after a migraine attack with aura Methods:…”
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Effectiveness of Low Vision Rehabilitation Using Microperimetric Acoustic Biofeedback Training in Patients with Central Scotoma by Sahli, Esra, Altinbay, Deniz, Bingol Kiziltunc, Pınar, Idil, Aysun

“…To evaluate the efficacy of visual rehabilitation with microperimeter biofeedback in patients with central scotoma. 35 consecutive patients with central…”
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Orbital Fibrotic Band as Cause of Monocular Elevation Deficiency by Atilla, Huban, Çaliş Karanfil, Feyza, Bingöl Kiziltunç, Pinar

“…Monocular elevation deficiency is a congenital, unilateral inability of elevation. It is classified as innervational, restrictive, or combine types. Here, we…”
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Evaluation of fixation characteristics in amblyopia using microperimetry by Altinbay, Deniz, Sahli, Esra, Bingol Kiziltunc, Pinar, Atilla, Huban

“…Purpose To evaluate fixation characteristics in amblyopia using macular analyzer integrity assessment (MAIA) microperimetry and to investigate the factors…”
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Diplopia due to acquired Brown syndrome after COVID-19 infection by Kızıltunç, Pınar Bingöl, Seven, Mehmet Yunus, Atilla, Huban

“…Coronavirus disease 2019 (COVID-19) is a multisystem, inflammatory condition usually presenting with respiratory symptoms, such as fever, shortness of breath,…”
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Chromatographic Analysis of Aqueous Humor of Bupivacaine in Different Administration Approaches by Dinçel, Aysun, Kızıltunç, Pınar Bingöl, Atilla, Huban, Onur, Feyyaz, Demirel, Sibel

“…Abstract Different administration approaches were investigated for the selection of bupivacaine administration type and a sensitive high-performance liquid…”
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Direct and transsynaptic retrograde degeneration and optic nerve head microvascular changes in patients with hemianopia by Celik Buyuktepe, Tuna, Bingöl Kızıltunç, Pınar, Buyuktepe, Murat, Atilla, Huban

“…Purpose: To investigate optic nerve head (ONH) microvascular changes secondary to transsynaptic retrograde degeneration (TRD), comperatively with direct…”
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Reappearance of excentric persistent fetal vasculature stalk following laser treatment in a patient with type 1 retinopathy of prematurity by Çalış Karanfil, Feyza, Bingöl Kızıltunç, Pınar, Özdemir Zeydanlı, Ece, Atilla, Huban, Özdek, Şengül

“…Purpose In this report, we aim to present an unusual reappearance of hyaloidal artery remnant with atypical localization during the follow-up of an infant who…”
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Isolated abducens nerve palsy due to COVID-19 by Bingöl Kızıltunç, Pınar, Seven, Mehmet Yunus, Atilla, Huban

“…Although coronavirus disease-2019 (COVID-19) is mainly a respiratory system disease, neurological complications due to peripheral and central nervous system…”
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Diplopia After Migraine Surgery by Celik Buyuktepe, Tuna, Bingöl Kiziltunç, Pinar, Atilla, Huban

“…A 46-year-old man with refractory migraine headache was treated with decompressive migraine surgery of the supraorbital and supratrochlear nerves…”
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Demographic, ocular and associated neurological findings in corpus callosum malformations by Kızıltunç, Pınar Bingöl, Şahlı, Esra, İdil, Aysun, Atilla, Huban

“…The corpus callosum is a primary commissural part of the brain which connects the two hemispheres. Processing sensory, motor, visuo-motor and cognitive…”
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A Report on Children with CEP290 Mutation, Vision Loss, and Developmental Delay by Sahli, Esra, Kiziltunc, Pinar Bingol, Idil, Aysun

“…[LANGUAGE= "English"] Mutations in CEP290, which encodes a centrosomal protein, cause Joubert syndrome, retinal dystrophy, and several other manifestations…”
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