Berna Şeker-Yılmaz

Four Gaucher disease type II patients with three novel mutations: a single centre experience from Turkey

D. Kör, S. Ceylaner, F. Bulut, 2018, Metabolic Brain Disease.

Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations.

A. Topaloğlu, B. Yüksel, D. Kör, 2017, The Turkish journal of pediatrics.

The outcome of 41 Late-Diagnosed Turkish GA-1 Patients: A Candidate for the Turkish NBS

F. Incecik, G. Ceylaner, S. Kılavuz, 2021, Neuropediatrics.

A 6-Month-Old Boy with Reddish, Scaly Skin: Netherton Syndrome

M. Yılmaz, D. Altintas, D. Kör, 2018, The Journal of Pediatric Research.

Four Gaucher disease type II patients with three novel mutations: a single centre experience from Turkey

D. Kör, S. Ceylaner, S. Kılavuz, 2018, Metabolic Brain Disease.

Genotypic and phenotypic features of the cystinosis patients from the South Eastern part of Turkey.

N. Cengiz, A. Anarat, A. Topaloğlu, 2016, The Turkish journal of pediatrics.

p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency.

D. Kör, S. Ceylaner, Gökhan Tümgör, 2017, The Turkish journal of pediatrics.