A 12-Year-Old Girl with Bilateral Coats Disease and ABCA4 Gene Mutation

por Saatci, Ali Osman, Ayhan, Ziya, Yaman, Aylin, Bora, Elcin, Ulgenalp, Ayfer, Kavukcu, Salih
Publicado 2018

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

Risk factors for subclinical inflammation in children with familial mediterranean fever

por Soylu, Alper, Bayram, Meral Torun, Çankaya, Tufan, Bora, Elçin, Kavukçu, Salih, Ülgenalp, Ayfer, Türkmen, Mehmet
Publicado 2014

Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development

por AKSEL KILIÇARSLAN, Özge, ATAMAN, Esra, GÜRSOY, Semra, GÜRBÜZ, Gürkan, ÜNALP, Aycan, GENÇPINAR, Pınar, OLGAÇ DÜNDAR, Nihal, EDİZER, Selvinaz, ÜLGENALP, Ayfer, GİRAY BOZKAYA, Özlem
Publicado 2020

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

Selective Bilateral Vestibular Neuropathy in a Turkish CMT1B Family With a Novel MPZ Mutation

por Akdal, Gülden, Koçoğlu, Koray, Bora, Elçin, Koç, Altuğ, Ülgenalp, Ayfer, Bedir, Mithat, Ala, Rahmi Tümay, Battaloğlu, Esra, Kırkım, Günay, Şengün, İhsan Şükrü, Halmágyi, Gábor Michael
Publicado 2021