Search Results - "Soner Keskin"

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  1. 1

    Evaluation of the Nerve Fiber Layer and Macula in the Eyes of Healthy Children Using Spectral-Domain Optical Coherence Tomography by Turk, Adem, Ceylan, Osman Melih, Arici, Ceyhun, Keskin, Soner, Erdurman, Cuneyt, Durukan, Ali Hakan, Mutlu, Fatih Mehmet, Altinsoy, Halil Ibrahim

    Published in American journal of ophthalmology (01-03-2012)
    “…Purpose To determine the normative values of the peripapillary retinal nerve fiber layer (RNFL), macular thickness, and macular volume in healthy children…”
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    Journal Article
  2. 2

    Bilateral Congenital Retinal Macrovessel: A Case Report by Ismaeel, Dalal, Keskin, Soner, Dallali, Foued

    Published in Curēus (Palo Alto, CA) (08-01-2023)
    “…Congenital retinal macrovessel (CRM) is a congenital anomaly where an aberrant vessel supplies both the macula on either side of the horizontal raphe. It is…”
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    Journal Article
  3. 3

    Comparison of the refractive measurements with hand-held autorefractometer, table-mounted autorefractometer and cycloplegic retinoscopy in children by Akil, Handan, Keskin, Soner, Çavdarli, Cemal

    Published in Korean journal of ophthalmology (01-06-2015)
    “…To evaluate the performance of the hand-held and table-top autorefractokeratometer in measuring refractive errors by comparing them with cycloplegic…”
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    Journal Article
  4. 4

    Comparison of the Refractive Measurements with Hand-held Autorefractometer, Table-mounted Autorefractometer and Cycloplegic Retinoscopy in Children by Handan Akil, Soner Keskin, Cemal Cavdarli

    Published in Korean journal of ophthalmology (05-06-2015)
    “…Purpose: To evaluate the performance of the hand-held and table-top autorefractokeratometer in measuring refractive errors by comparing them with cycloplegic…”
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    Journal Article
  5. 5

    A case of autoimmune polyendocrine syndrome type 1 with ocular findings and unique AIRE gene defect by Handan Akil, Ayse Derya Bulus, Nesibe Andiran, Pascale Saugier Veber, Soner Keskin

    “…Autoimmune polyendocrine syndrome type 1 (APS 1) is a rare autosomal recessive disorder that is characterized by autoimmunity against endocrine and ectodermal…”
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    Journal Article
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    A case of autoimmune polyendocrine syndrome type 1 with ocular findings and unique AIRE gene defect by Akil, Handan, Bulus, Ayse, Andiran, Nesibe, Veber, Pascale, Keskin, Soner

    “…Autoimmune polyendocrine syndrome type 1 (APS 1) is a rare autosomal recessive disorder that is characterized by autoimmunity against endocrine and ectodermal…”
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    Journal Article
  8. 8

    Reply by Turk, Adem, Ceylan, Osman Melih, Arici, Ceyhun, Keskin, Soner, Erdurman, Cuneyt, Durukan, Ali Hakan, Mutlu, Fatih Mehmet, Altinsoy, Halil Ibrahim

    Published in American journal of ophthalmology (01-04-2012)
    “…[...]we would like to thank Huang and associates for their interest in our article.1 It is well known that ocular characteristics of children vary with…”
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    Journal Article
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