Showing 1 - 7 results of 7 for search 'Handan Guleryuz', query time: 0.01s Refine Results
  1. 1
    A newborn with monosomy X in association with corpus callosum agenesis

    A newborn with monosomy X in association with corpus callosum agenesis by Duygu Onur Cura, Burcin Iscan, Semra Gursoy, Handan Guleryuz, Tufan Cankaya, Tulay Ozturk, Ozlem Giray Bozkaya

    Published 2017-10-01
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  2. 2
    Rotavirus encephalopathy with concomitant acute cerebellitis: report of a case and review of the literature

    Rotavirus encephalopathy with concomitant acute cerebellitis: report of a case and review of the literature by Cem Paketçi, Pınar Edem, Derya Okur, Fatma Ceren Sarıoğlu, Handan Güleryüz, Erhan Bayram, Semra Hız Kurul, Uluç Yiş

    Published 2020-02-01
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  3. 3
    The prognostic role of prenatal MRI volumetric assessment in fetuses with isolated ventriculomegaly

    The prognostic role of prenatal MRI volumetric assessment in fetuses with isolated ventriculomegaly by Naciye Sinem Gezer, Handan Güleryüz, Cenk Gezer, Ali Koçyiğit, Didem Yeşilırmak, Atalay Ekin, Muzaffer Bilgin, İbrahim Egemen Ertaş

    Published 2015-06-01
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  4. 4
    Importance of neurologic and cutaneous signs in the diagnosis of Schimke immuno-osseous dysplasia

    Importance of neurologic and cutaneous signs in the diagnosis of Schimke immuno-osseous dysplasia by Ayşe İpek Polat, Uluç Yiş, Müge Ayanoğlu, Ayşe Semra Hız, Handan Güleryüz, Tülay Öztürk Atasoy, Cornelius F Boerkoel

    Published 2015-10-01
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  5. 5
    Evaluation of Associated Structural and Chromosomal Abnormalities in Patients with Fetal Cerebral Ventriculomegaly Detected in Ultrasonographic Imaging

    Evaluation of Associated Structural and Chromosomal Abnormalities in Patients with Fetal Cerebral Ventriculomegaly Detected in Ultrasonographic Imaging by Erkan Cagliyan, Samican Ozmen, Sureyya Saridas Demir, Ceren Aydin, Egehan Bilen, Handan Guleryuz, Elif Yasar, Derya Ercal, Elcin Bora, Tufan Cankaya

    Published 2022-12-01
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  6. 6
    GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria

    GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria by Tülay Öncü-Öner, Semra Hız-Kurul, Bayram Yüksel, Bekir Ergüner, Aydan Saraç, Handan Güleryüz, Sinem Ağılkaya, İlknur Porsuk-Doru, Aycan Ünalp, Sultan Cingöz

    Published 2018-06-01
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  7. 7
    Functional divergence of the two Elongator subcomplexes during neurodevelopment

    Functional divergence of the two Elongator subcomplexes during neurodevelopment by Monika Gaik, Marija Kojic, Megan R Stegeman, Tülay Öncü‐Öner, Anna Kościelniak, Alun Jones, Ahmed Mohamed, Pak Yan Stefanie Chau, Sazia Sharmin, Andrzej Chramiec‐Głąbik, Paulina Indyka, Michał Rawski, Anna Biela, Dominika Dobosz, Amanda Millar, Vann Chau, Aycan Ünalp, Michael Piper, Mark C Bellingham, Evan E Eichler, Deborah A Nickerson, Handan Güleryüz, Nour El Hana Abbassi, Konrad Jazgar, Melissa J Davis, Saadet Mercimek‐Andrews, Sultan Cingöz, Brandon J Wainwright, Sebastian Glatt

    Published 2022-06-01
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