Showing 1 - 13 results of 13 for search 'Serdar Ceylaner', query time: 0.01s Refine Results
  1. 1
    An infant with glutaric aciduria type IIc diagnosed with a novel mutation

    An infant with glutaric aciduria type IIc diagnosed with a novel mutation by Sedat Işıkay, Ayhan Yaman, Serdar Ceylaner

    Published 2017-06-01
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  2. 2
    Ataxia, tremor, intellectual disability: a case of STXBP1 encephalopathy with a new mutation

    Ataxia, tremor, intellectual disability: a case of STXBP1 encephalopathy with a new mutation by Aydan Değerliyurt, Gamze Gezgen Kesen, Serdar Ceylaner

    Published 2019-10-01
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  3. 3
    Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogenase deficiency

    Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogenase deficiency by Mustafa Kılıç, Saliha Şenel, Kadri Karaer, Serdar Ceylaner

    Published 2017-12-01
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  4. 4
    Brown Vialetto Van Laere syndrome: presenting with left ventricular non-compaction and mimicking mitochondrial disorders

    Brown Vialetto Van Laere syndrome: presenting with left ventricular non-compaction and mimicking mitochondrial disorders by Berna Şeker Yılmaz, Serdar Ceylaner, Neslihan Önenli Mungan

    Published 2021-04-01
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  5. 5
    Coexistence of a Leaky SCID Phenotype With Hyperphenylalaninemia in an Adult Case

    Coexistence of a Leaky SCID Phenotype With Hyperphenylalaninemia in an Adult Case by Ugur Musabak, Tuba Erdogan, Muserref Sule Akcay, Serdar Ceylaner

    Published 2025-01-01
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  6. 6
    Turkish cases of early infantile epileptic encephalopathy: two novel mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene

    Turkish cases of early infantile epileptic encephalopathy: two novel mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene by Sarenur Gökben, Gül Serdaroğlu, Sanem Yılmaz, Thierry Bienvenu, Serdar Ceylaner

    Published 2015-06-01
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  7. 7
    Neonatal form of biotin-thiamine-responsive basal ganglia disease. Clues to diagnosis

    Neonatal form of biotin-thiamine-responsive basal ganglia disease. Clues to diagnosis by Aydan Değerliyurt, Mehmet Gündüz, Serdar Ceylaner, Özlem Ünal, Sevim Ünal

    Published 2019-04-01
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  8. 8
    Siblings with Ethylmalonic Encephalopathy: Case Report

    Siblings with Ethylmalonic Encephalopathy: Case Report by Çiğdem Seher Kasapkara, Ayşe Aksoy, Emine Polat, Mustafa Kılıç, Serdar Ceylaner

    Published 2018-03-01
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  9. 9
    A case with a novel GATA1 variant mimicking immune thrombocytopenia attacks

    A case with a novel GATA1 variant mimicking immune thrombocytopenia attacks by Elif Habibe Aktekin, Serdar Ceylaner, Şeyda Beşen, Ayşe Erbay, Nalan Yazıcı

    Published 2025-12-01
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  10. 10
    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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  11. 11
    Pyridoxine-dependent epilepsy in two Turkish patients in Turkey and review of the literature

    Pyridoxine-dependent epilepsy in two Turkish patients in Turkey and review of the literature by Gülen Gül-Mert, Faruk İncecik, M Özlem Hergüner, Serdar Ceylaner, Şakir Altunbaşak

    Published 2015-08-01
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  12. 12
    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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  13. 13
    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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