Two siblings with galactose mutarotase deficiency: Clinical differencesHavva Yazıcı, Mahmut Çöker, Sema Kalkan Uçar et al.|JIMD Reports|2021Cited by 9
Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiencyMerve Yoldaş Çelik, Mahmut Çöker, Yasemin Atik Altınok et al.|Nutrition Metabolism and Cardiovascular Diseases|2024Cited by 7
Long‐term personalized high‐protein, high‐fat diet in pediatric patients with glycogen storage disease type <scp>IIIa</scp>: Evaluation of myopathy, metabolic control, physical activity, growth, and dietary complianceSema Kalkan Uçar, Mahmut Çöker, Merve Yoldaş Çelik et al.|Journal of Inherited Metabolic Disease|2024Cited by 6
One Year Experience of Pheburane® (Sodium Phenylbutyrate) Treatment in a Patient with Argininosuccinate Lyase DeficiencySema Kalkan Uçar, Mahmut Çöker, Burcu Özbaran et al.|JIMD Reports|2014Cited by 5
Glutaric Aciduria Type I Diagnosis Case with Normal Glutaryl Carnitine and Urine Organic Acid AnalysisEbru Canda, Mahmut Çöker, Havva Yazıcı et al.|The Journal of Pediatric Research|2018Cited by 3