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Journal of Pediatric Hematology/Oncology|September 29, 2006
Nutritional megaloblastic anemia in young Turkish children is associated with vitamin B-12 deficiency and psychomotor retardationSelahattin Katar, Mehmet Nuri Ozbek, Ahmet Yaramiş, et al.
Journal of Tropical Pediatrics|November 14, 2022
Neonatal classic galactosemia-diagnosis, clinical profile and molecular characteristics in unscreened Turkish populationMuhittin Çelik, Osman Akdeniz, Mehmet Nuri Ozbek, et al.
Journal of Clinical Research in Pediatric Endocrinology|September 28, 2013
Multiple pituitary hormone deficiency due to gunshot injury in a 6-year-old girlHüseyin Demirbilek, Mehmet Nuri Ozbek, Rıza Taner Baran, et al.
Neuro Endocrinology Letters|June 12, 2019
A Distinct Clinical Phenotype in Two Siblings with X-linked AdrenoleukodystrophyNilufer Ozdemir Kutbay, Mehmet Nuri Ozbek, Banu Sarer Yurekli, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|October 20, 2023
Evaluation and management of neonatal onset hyperinsulinemic hypoglycemia: a single neonatal center experienceHandan Bezirganoglu, Nilufer Okur, Kiymet Celik, et al.
European Journal of Pediatrics|March 22, 2019
Short-term results of continuous venovenous haemodiafiltration versus peritoneal dialysis in 40 neonates with inborn errors of metabolismMuhittin Celik, Osman Akdeniz, Nezir Ozgun, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|July 24, 2019
Early neurological complications in children with classical galactosemia and p.gln188arg mutationNezir Özgün, Muhittin Celik, Osman Akdeniz, et al.
Pediatric Diabetes|July 14, 2020
Neonatal diabetes due to homozygous INS gene promoter mutations: Highly variable phenotype, remission and early relapse during the first 3 years of lifeMeliha Demiral, Huseyin Demirbilek, Kıymet Çelik, et al.
Hormone Research in Paediatrics|March 17, 2016
Genotype and Phenotype Characteristics in 22 Patients with Vitamin D-Dependent Rickets Type ISophia Tahir, Hüseyin Demirbilek, Mehmet Nuri Ozbek, et al.
Journal of Pediatric Neurosciences|January 29, 2014
Unusual cause of hyperammonemia in two cases with short-term and long-term valproate therapy successfully treated by single dose carglumic acidCiğdem Seher Kasapkara, Murat Kanğın, Funda Feryal Taş, et al.
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