Browsing by Author
Özturk, Önder
Showing results 1 to 4 of 4
| Issue Date | Title | Author(s) |
| 2016 | Brain-derived neurotrophic factor gene val66met polymorphism is a risk factor for attention-deficit hyperactivity disorder in a Turkish sample | Özturk, Önder; Başay, Bürge Kabukçu; Büber, Ahmet ; Başay, Ömer ; Alaçam, Hüseyin ; Bacanli, A.; Yilmaz, Ş.G. |
| 2016 | The effect of single dose methylphenidate on neurometabolites according to COMT gene Val158Met polymorphism in the patient with attention deficit hyperactivity disorder: A study using magnetic resonance spectroscopy | Özturk, Önder; Alaçam, Hasan; Başay, Bürge Kabukçu; Başay, Ömer ; Büber, Ahmet ; Ay, Özlem İzci; Aglad'Oglu, K. |
| 2016 | Oxidative imbalance in children and adolescents with autism spectrum disorder | Özturk, Önder; Başay, Ömer ; Başay, Bürge Kabukçu; Alaçam, Hüseyin ; Büber, Ahmet ; Kaptanoglu, B.; Enli, Yaşar |
| 2016 | White matter alterations related to attention-deficit hyperactivity disorder and COMT val158met polymorphism: Children with valine homozygote attention-deficit hyperactivity disorder have altered white matter connectivity in the right cingulum (cingulate gyrus) | Kabukçu Başay, Bürge ; Büber, Ahmet ; Başay, Ömer ; Alaçam, Hüseyin ; Özturk, Önder; Suren, S.; Ay, O.I. |
