Buber, A
Buber, A.
Büber, A
Büber, A.
Results 1-4 of 4 (Search time: 0.01 seconds).
Issue Date | Title | Author(s) | |
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1 | 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. |
2 | 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 |
3 | 2020 | The prevalence and comorbidity rates of specific learning disorder among primary school children in Turkey | Büber, Ahmet ; Başay, Ömer ; Şenol, Hande |
4 | 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. |
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