Showing 1 - 9 results of 9 for search 'Ali Dursun', query time: 0.27s Refine Results
  1. 1
    Late-diagnosed phenylketonuria in an eight-year-old boy with dyslexia and attention-deficit hyperactivity disorder

    Late-diagnosed phenylketonuria in an eight-year-old boy with dyslexia and attention-deficit hyperactivity disorder by Yılmaz Yıldız, Ali Dursun, Ayşegül Tokatlı, Turgay Coşkun, Hatice Serap Sivri

    Published 2016-02-01
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  2. 2
    Molecular genetics of maple syrup urine disease in the Turkish population

    Molecular genetics of maple syrup urine disease in the Turkish population by Kerstin Gorzelany, Ali Dursun, Turgay Coşkun, Serap H Kalkanoğlu-Sivri, Gülden Fatma Gökçay, Mübeccel Demirkol, Oliver Feyen, Udo Wendel

    Published 2009-04-01
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  3. 3
    Comprehensive analysis of 1103 infants referred to a single center due to positive newborn screening test for phenylketonuria

    Comprehensive analysis of 1103 infants referred to a single center due to positive newborn screening test for phenylketonuria by Ayça Burcu Kahraman, Kısmet Çıkı, Begüm Poşul, Mustafa Güvercin, Yılmaz Yıldız, Ali Dursun, Serap Sivri, Turgay Coşkun, Ayşegül Tokatlı

    Published 2025-05-01
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  4. 4
    Cobalamin C defect: a patient of late-onset type with homozygous p.R132* mutation

    Cobalamin C defect: a patient of late-onset type with homozygous p.R132* mutation by Mustafa Kılıç, Rıza Köksal Özgül, Ali Dursun, Ayşegül Tokatlı, Hatice Serap Kalkanoğlu-Sivri, Banu Anlar, Brian Fowler, Turgay Coşkun

    Published 2013-12-01
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  5. 5
    Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation

    Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation by Özlem Ünal, R Köksal Özgül, Didem Yücel, Dilek Yalnızoğlu, Ayşegül Tokatlı, H Serap Sivri, Burcu Hişmi, Turgay Coşkun, Ali Dursun

    Published 2015-08-01
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  6. 6
    3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures

    3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures by Turgay Coşkun, Halil Ibrahim Aydin, Mustafa Kiliç, Ali Dursun, Göknur Haliloğlu, Haluk Topaloğlu, Kader Karli-Oğuz, Tom J De Koning

    Published 2009-12-01
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  7. 7
    Clinical and molecular characteristics of carnitineacylcarnitine translocase deficiency with c.270delC and a novel c.408C>A variant

    Clinical and molecular characteristics of carnitineacylcarnitine translocase deficiency with c.270delC and a novel c.408C>A variant by Berrak Bilginer Gürbüz, Didem Yücel Yılmaz, Rıza Köksal Özgül, Can Koşukcu, Ali Dursun, Hatice Serap Sivri, Turgay Coşkun, Ayşegül Tokatlı

    Published 2021-08-01
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  8. 8
    Sapropterin dihydrochloride treatment in Turkish hyperphenylalaninemic patients under age four

    Sapropterin dihydrochloride treatment in Turkish hyperphenylalaninemic patients under age four by Özlem Ünal, Hülya Gökmen-Özel, Turgay Coşkun, R Köksal Özgül, Didem Yücel, Burcu Hişmi, Ayşegül Tokatlı, Ali Dursun, H Serap Sivri

    Published 2015-06-01
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  9. 9
    A novel mutation in the DGUOK gene in a Turkish newborn with mitochondrial depletion syndrome

    A novel mutation in the DGUOK gene in a Turkish newborn with mitochondrial depletion syndrome by Mustafa Kiliç, Haluk Topaloğlu, Sule Yiğit, Zuhal Akçören, Sara Seneca, Linda De Meirleir, Ayşegül Tokatli, Ali Dursun, Hatice Serap Sivri, Turgay Coşkun

    Published 2011-02-01
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