The Turkish Journal of Pediatrics
2022 , Vol 64 , Num 4
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.
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.
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.
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.
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.
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.