Search Results - Baykal, Tolunay

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  1. 1
    Molecular genetics and impact of residual in vitro phenylalanine hydroxylase activity on tetrahydrobiopterin responsiveness in Turkish PKU population

    Molecular genetics and impact of residual in vitro phenylalanine hydroxylase activity on tetrahydrobiopterin responsiveness in Turkish PKU population by Dobrowolski, Steven F., Heintz, Caroline, Miller, Trent, Ellingson, Clinton, Ellingson, Clifford, Özer, Işıl, Gökçay, Gulden, Baykal, Tolunay, Thöny, Beat, Demirkol, Mübeccel, Blau, Nenad

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  2. 2
    Corticospinal Tract Involvement in a Patient With 3-HMG Coenzyme A Lyase Deficiency

    Corticospinal Tract Involvement in a Patient With 3-HMG Coenzyme A Lyase Deficiency by Yýlmaz, Yüksel, Özdemir, Nihal, Ekinci, Gazanfer, Baykal, Tolunay, Kocaman, Canan

    Published in Pediatric neurology
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  3. 3
    Screening for tetrahydrobiopterin deficiencies using dried blood spots on filter paper

    Screening for tetrahydrobiopterin deficiencies using dried blood spots on filter paper by Zurflüh, Marcel R., Giovannini, Marcello, Fiori, Laura, Fiege, Betina, Gokdemir, Yasemin, Baykal, Tolunay, Kierat, Lucja, Gärtner, Konrad H., Thöny, Beat, Blau, Nenad

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  4. 4
    Biotinidase deficiency: Novel mutations and their biochemical and clinical correlates

    Biotinidase deficiency: Novel mutations and their biochemical and clinical correlates by Wolf, Barry, Jensen, Kevin P., Barshop, Bruce, Blitzer, Miriam, Carlson, Martha, Goudie, David R., Gokcay, Gulden Huner, Demirkol, Mubeccel, Baykal, Tolunay, Demir, F., Quary, Sharon, Shih, Ling Yu, Pedro, Helio F., Chen, Tsui-hua H., Slonim, Alfred E.

    Published in Human mutation
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  5. 5
    Stroke in Childhood: Experience in Istanbul, Turkey

    Stroke in Childhood: Experience in Istanbul, Turkey by Aydinli, Nur, Tatli, Burak, Çalişkan, Mine, Özmen, Meral, Citak, Agop, Unuvar, Aysegul, Baykal, Tolunay, Omeroglu, Rukiye Eker, Aydin, Kubilay, Sencer, Serra, Sencer, Altay, Kırış, Talat

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  6. 6
    Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE)

    Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE) by ROMSTAD, Anne, KALKANOGLU, H. Serap, COSKUN, Turgay, DEMIRKOL, Mübeccel, TOKATLI, Aysegül, DURSUN, Ali, BAYKAL, Tolunay, ÖZALP, Imran, GULDBERG, Per, GÜTTLER, Flemming

    Published in Human genetics
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