Showing 1 - 8 results of 8 for search 'Deniz Kor', query time: 0.02s Refine Results
  1. 1
    Blue-colored sweating: four infants with apocrine chromhidrosis

    Blue-colored sweating: four infants with apocrine chromhidrosis by Ahmet Yöntem, Deniz Kör, Bircan Hızlı-Karabacak, Mehmet Karakaş, Neslihan Önenli-Mungan

    Published 2015-06-01
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  2. 2
    p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency

    p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency by Berna Şeker-Yılmaz, Deniz Kör, Gökhan Tümgör, Serdar Ceylaner, Neslihan Önenli-Mungan

    Published 2017-06-01
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  3. 3
    X-linked adrenoleukodystrophy in a 6-year-old boy initially presenting with psychiatric symptoms

    X-linked adrenoleukodystrophy in a 6-year-old boy initially presenting with psychiatric symptoms by Faruk İncecik, M Özlem Hergüner, Gülen Mert, Neslihan Önenli-Mungan, Serdar Ceylaner, Deniz Kör, Şakir Altunbaşak

    Published 2014-12-01
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  4. 4
    Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations

    Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations by Deniz Kör, Berna Şeker-Yılmaz, Fatma Derya Bulut, Sebile Kılavuz, Murat Öktem, Serdar Ceylaner, Dinçer Yıldızdaş, Neslihan Önenli-Mungan

    Published 2019-06-01
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  5. 5
    Clinical features and rare complications in 132 patients with hepatic glycogenosis

    Clinical features and rare complications in 132 patients with hepatic glycogenosis by Deniz Kor, Fatma Derya Bulut, Burcu Köşeci, Esra Kara, Ezgi Burgaç, İrem Kaplan, Nazmiye Tüzel Gündüz, Halise Neslihan Önenli Mungan

    Published 2025-08-01
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  6. 6
    Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders

    Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders by Sebile Kılavuz, Fatma Derya Bulut, Deniz Kor, Berna Şeker Yılmaz, Atıl Bişgin, Fadli Demir, Bahriye Atmış, Derya Alabaz, Neslihan Mungan, Mustafa Yılmaz

    Published 2023-09-01
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  7. 7
    Genotypic and phenotypic features of the cystinosis patients from the South Eastern part of Turkey

    Genotypic and phenotypic features of the cystinosis patients from the South Eastern part of Turkey by Neslihan Önenli-Mungan, Bilgin Yüksel, Ali Kemal Topaloğlu, Berna Şeker-Yılmaz, Gülay Ceylaner, Aytül Noyan, Sevgi Yavuz, Nurcan Cengiz, Aysun Karabay-Bayazıt, Deniz Kör, Ali Anarat

    Published 2016-08-01
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  8. 8
    A comprehensive integrated disease management program for phenylketonuria (IDMP-PKU) from Türkiye: rationale, design and patient characteristics

    A comprehensive integrated disease management program for phenylketonuria (IDMP-PKU) from Türkiye: rationale, design and patient characteristics by Mehmet Cihan Balci, Deniz Kor, Yilmaz Yildiz, Meryem Karaca, Fatma Derya Bulut, Ayca Burcu Kahraman, Alihan Yesil, Ezgi Burgac, Kismet Ciki, Arzu Selamioglu, Burcu Koseci, Asli Durmus, Irem Kaplan, Esra Kara, Halise Neslihan Mungan, Serap Sivri, Gulden Fatma Gokcay, Aysegul Tokatli, Mubeccel Demirkol, Turgay Coskun, Imran Ozalp

    Published 2025-08-01
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