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The Turkish Journal of Pediatrics|October 3, 2007
Malformations of cortical development: clinical spectrum in a series of 101 patients and review of the literature (Part I)Serdal Güngör, Dilek Yalnizoğlu, Güzide Turanli, et al.The Turkish Journal of Pediatrics|May 4, 2011
Learning disability and oligodendrocyte myelin glycoprotein (OMGP) gene in neurofibromatosis type 1Yunus Kasim Terzi, Sibel Oğuzkan-Balci, Banu Anlar, et al.The Turkish Journal of Pediatrics|October 3, 2007
Malformations of cortical development and epilepsy: evaluation of 101 cases (part II)Serdal Güngör, Dilek Yalnizoğlu, Güzide Turanli, et al.The Turkish Journal of Pediatrics|March 4, 2010
Cognitive functions in neurofibromatosis type 1 patients and unaffected siblingsEmel Erdoğan-Bakar, Mine Cinbiş, Hamit Ozyürek, et al.Journal of Clinical Research in Pediatric Endocrinology|March 8, 2012
Neurocognitive functions in children and adolescents with subclinical hypothyroidismAyça Törel Ergür, Yasemen Taner, Evşen Ata, et al.Pageof 2