N. Önenli Mungan

Evaluation of bone health in patients with mucopolysaccharidosis

Ö. Kaya, G. Seydaoglu, S. Başaran, 2022, Journal of Bone and Mineral Metabolism.

Coexistence of molybdenum cofactor deficiency type A and hypertrophic pyloric stenosis, a new case

M. Satar, F. Özlü, H. Yıldızdaş, 2021, Turkish archives of pediatrics.

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

S. Poyrazoglu, A. Topaloğlu, L. D. Kotan, 2012, Journal of Clinical Research in Pediatric Endocrinology.

Tyrosinemia type 1 and irreversible neurologic crisis after one month discontinuation of nitisone

F. Incecik, D. Yıldızdaş, Ö. Horoz, 2016, Metabolic Brain Disease.

Perspectives of adult patients with lysosomal storage diseases on the transition from pediatric to adult healthcare in Turkey.

G. Seydaoglu, F. Bulut, S. Kılavuz, 2023, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.