Now showing items 1-3 of 3

    • Evaluation of Etiologic and Prognostic Factors in Neonatal Convulsions 

      Tatli, Burak; Caliskan, Mine; Aydinli, Nur; Eraslan, Emine; Ekici, Baris; Yildiz, Edibe Pembegul; Ozmen, Meral (2012-09-01)
      This study evaluated etiologic and risk factors affecting long-term prognoses of neurologic outcomes in newborns with neonatal seizures. We enrolled patients at chronologic ages of 23-44 months, referred to the Department ...
    • Hereditary spastic paraplegia type 35 caused by a novel FA2H mutation 

      Bektas, Gonca; Yesil, Gozde; Ozmen, Meral; Caliskan, Mine; Aydinli, Nur; Yildiz, Edibe Pembegul (2017-05-01)
      Hereditary spastic paraplegia type 35 (SPG35) is a rare disorder characterized by progressive spasticity. Mutations in the fatty acid 2-hydroxylase (FA2H) gene in different loci are responsible for phenotypic variability. ...
    • Vanishing white matter disease with a novel EIF2B5 mutation: A 10-year follow-up 

      Bektas, Gonca; Uzunhan, Tugce Aksu; Yildiz, Edibe Pembegul; Ozkan, Melis Ulak; YEŞİL, GÖZDE; Caliskan, Mine (2018-08-01)
      Background: Vanishing white matter disease is a heterogeneous disorder caused by mutation in one of the five genes encoding subunits of the eukaryotic initiation factor eIF2B. It is a heterogeneous disorder due to phenotypic ...