N. Önenli-Mungan

发表

X-linked adrenoleukodystrophy in a 6-year-old boy initially presenting with psychiatric symptoms.

F. Incecik, D. Kör, M. O. Hergüner, 2014, The Turkish journal of pediatrics.

Thyroid Hormone Levels and their Relationship to Survival in Children with Bacterial Sepsis and Septic Shock

Y. Sertdemir, B. Yüksel, D. Yıldızdaş, 2004 .

Growth hormone and insulin‐like growth factor 1 levels and their relation to survival in children with bacterial sepsis and septic shock

A. Topaloğlu, B. Yüksel, D. Yıldızdaş, 2004, Journal of paediatrics and child health.

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.

Serum IL-1, IL-2, TNFα and INFγ Levels of Patients with Type 1 Diabetes Mellitus and their Siblings

B. Yüksel, M. Yılmaz, S. Çetiner, 2003 .

Stature Due to Growth Hormone Neurosecretory Dysfunction in a Child with Major Depressive Disorder

A. Avcı, N. Önenli-Mungan, K. Topaloğlu, 2004 .

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.

Blue-colored sweating: four infants with apocrine chromhidrosis.

M. Karakaş, D. Kör, N. Önenli-Mungan, 2015, The Turkish journal of pediatrics.

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.

Coexistence of 2 rare autosomal recessively inherited disorders manifesting with immune deficiency; IL-12 receptor β1 and biotinidase deficiencies.

M. Yılmaz, D. Altintas, D. Doğruel, 2018, 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.