Single center experience of biotinidase deficiency: 259 patients and six novel mutationsEbru Canda, Mahmut Çöker, Havva Yazıcı et al.|Journal of Pediatric Endocrinology and Metabolism|2018Cited by 37
Clinical, biochemical, and molecular insights into Cerebrotendinous Xanthomatosis: A nationwide study of 100 Turkish individualsTanyel Zübarioğlu, Ayşe Çiğdem Aktuğlu Zeybek, Ertuğrul Kıykım et al.|Molecular Genetics and Metabolism|2024Cited by 19
Tetrahydrobiopterin deficiencies: Lesson from clinical experienceAyşe Ergül Bozacı, Mahmut Çöker, Esra Er et al.|JIMD Reports|2021Cited by 16
Two siblings with galactose mutarotase deficiency: Clinical differencesHavva Yazıcı, Mahmut Çöker, Ebru Canda et al.|JIMD Reports|2021Cited by 9
An Evalution of the Demographic and Clinical Characterictics of Patients with GM2 GangliosidosisEsra Er, Mahmut Çöker, Ebru Canda et al.|The Journal of Pediatric Research|2018Cited by 7