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Pediatric Neurology|February 6, 2020
Brainstem auditory-evoked potentials in iron-deficiency anemiaS Ümit Sarici, Muhittin A Serdar, M Rusen Dündaröz, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|May 30, 2015
A rare cause of fatal pulmonary alveolar proteinosis: Niemann-Pick disease type C2 and a novel mutationAyhan Yaman, Fatma T Eminoğlu, Tanıl Kendirli, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 21, 2007
Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 geneSerap Teber, Taner Sezer, Mehpare Kafali, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 9, 2005
Relationship between plasma leptin, insulin and tumor necrosis factor alpha in obese childrenZehra Aycan, Merih Berberoğlu, Gönül Ocal, et al.Pediatric Hematology and Oncology|January 15, 2002
Recurrent arterial thrombosis in a child: primary antiphospholipid antibody syndromeZümrüt Uysal, Figen Doğu, A Emin Kürekçi, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 5, 2015
Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiencyBuket Dönmez-Demir, Tiraje Celkan, Nazan Sarper, et al.Frontiers in Neurology|April 11, 2025
Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohortÖmer Bektaş, Murat Gülşen, Onur Burak Dursun, et al.Pageof 5