Lack of Association of Childhood Partial Epilepsy with Brain Derived Neurotrophic Factor Gene

por Unalp, Aycan, Bora, Elcin, Cankaya, Tufan, Giray Bozkaya, Ozlem, Ercal, Derya, Ozturk, Aysel, Ulgenalp, Ayfer
Publicado 2012

The ASXL1 mutation p.Gly646Trpfs*12 found in a Turkish boy with Bohring‐Opitz Syndrome

por Urreizti, Roser, Gürsoy, Semra, Castilla‐Vallmanya, Laura, Cunill, Guillem, Rabionet, Raquel, Erçal, Derya, Grinberg, Daniel, Balcells, Susana
Publicado 2018

Identification of PCDH19 Gene Mutations/Deletions in Patients with Early Onset Epilepsy

por Gursoy, Semra, Ataman, Esra, Baysal, Bahar Toklu, Özyılmaz, Berk, Gençpınar, Pınar, Hız, Ayşe Semra, Yiş, Uluç, Ünalp, Aycan, Dündar, Nihal Olgaç, Ülgenalp, Ayfer, Erçal, Derya
Publicado 2020