Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiencyMerve Yoldaş Çelik, Mahmut Çöker, Ebru Canda 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
Splenomegaly and progressive neurologic involvement: Think about Niemann–Pick type C diseaseMerve Yoldaş Çelik, Mahmut Çöker, Havva Yazıcı et al.|Pediatrics International|2024Cited by 4
Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic formHavva Yazıcı, Mahmut Çöker, Güneş Ak et al.|Journal of Pediatric Endocrinology and Metabolism|2023Cited by 3
Unique clinical presentations and follow-up outcomes from experience with congenital disorders of glycosylation: PMM2-PGM1-DPAGT1-MPI-POMT2-B3GALNT2-DPM1-SRD5A3-CDGMerve Yoldaş Çelik, Mahmut Çöker, Havva Yazıcı et al.|Journal of Pediatric Endocrinology and Metabolism|2023Cited by 3