Volume 64 Issue 4 (2022)

Published: August 28, 2022

Original Articles

Association between serum vitamin A, D and E status and respiratory distress syndrome in preterm infants - a propensity score matching analysis
Evaluation of ciliary functions and ciliary beat frequency via cell culture method in patients with primary ciliary dyskinesia
Computed tomography findings of COVID-19 in pediatric patients
Imaging manifestations of neonatal necrotizing enterocolitis to predict timing of surgery
Evaluation of the predictability of clinical and radiological findings in the diagnosis of malrotation
Early predictors of high-flow nasal cannula oxygen treatment failure in patients with respiratory distress admitted to the pediatric emergency department
Assessment of auditory functions in patients with hepatic glycogen storage diseases
Identifying the effects of excess weight, metabolic syndrome and insulin resistance on liver stiffness using ultrasound elastography in children
Development of preschool refugee children living under temporary protection status
The role of self-discontentment and impulsivity for youth smoking behavior, nicotine dependence and future smoking intention in a clinical sample of Turkish adolescents
Is vasoactive-inotropic score associated with early lactate clearance a predictive outcome of children with septic shock?
Comparison of pediatric antibiotic prescribing practice between low and high prescribers for children in primary care

Case Reports

A rare case of hypomyelinating leukodystrophy-14 benefiting from ketogenic diet therapy
A pediatric bithalamic high grade glioma with concomitant H3K27M and EGFR mutations
The challenge to prove a rare cause of secondary arterial hypertension. A case report of a pediatric renal solitary fibrous tumor
Sirolimus treatment of a PTEN hamartoma tumor syndrome presenting with melena
Recovery of cyanosis after esophageal intubation in a neonate with tracheal agenesis: a case report
AA amyloidosis presenting with acute kidney injury, curable or not?
Optic neuritis in CD59 deficiency: an extremely rare presentation
Fucosidosis: clinical and molecular findings of Turkish patients
Autosomal chromosome microdeletions in three adolescent girls with premature ovarian insufficiency: a case report
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
Rare cause of ketolysis: Monocarboxylate transporter 1 deficiency