The Turkish Journal of Pediatrics 2018 , Vol 60 , Num 5
Non-immune hydrops fetalis: A retrospective analysis of 151 autopsies performed at a single center.

Ultrasound guided percutaneous central venous catheters in neonatal intensive care unit.

Effects of Lactobacillus rhamnosus GG as a probiotic on neonatal hyperbilirubinemia.

Outcome of out-of-hospital cardiopulmonary arrest in children: A multicenter cohort study.

Perioperative factors associated with hyperglycemia after pediatric cardiac surgery and impact of hyperglycemia on morbidity and mortality.

Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome.

Investigation of antiviral resistance and escape mutations in children with naive chronic hepatitis B patients and their parents.

Does microbial resistance profile change in community-based intra-abdominal infections? Evaluation of the culture results of patients with appendicitis.

Plasma lipoxin A4 levels in childhood chronic spontaneous urticaria.

Exhaled breath condensate magnesium levels of infants with bronchiolitis.

Folate deficiency in patients with classical galactosemia: A novel finding that needs to be considered for dietary treatments.

Frequency and findings of the acquired anorectal disease in the pediatric population with chronic constipation.

Evaluation of psychological characteristics of Turkish children with type 1 diabetes mellitus from two demographically and geographically distinct regions.

Asymptomatic intracranial hemorrhage in a newborn with congenital factor VII deficiency and successful treatment with recombinant activated factor VII.

Treatment of severe leptospirosis with therapeutic plasma exchange in a pediatric patient.

Fever-induced Brugada syndrome in a 9-year-old boy presenting with acute chest pain.

A girl with Henoch Schönlein purpura associated with acute rheumatic fever and review of literature.

Glycogen storage disease type 0 due to a novel frameshift mutation in glycogen synthase 2 (GYS2) gene in a child presenting with fasting hypoglycemia and postprandial hyperglycemia.

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

A novel mutation of interleukin-1 receptor antagonist (IL1RN) in a DIRA patient from Turkey: Diagnosis and treatment.

An extreme entity in differential diagnosis of musculoskeletal involvement-fibrodysplasia ossificans progressiva: a case based review.

Sustained hyperferritinemia in a child with macrophage activation syndrome secondary to systemic juvenile idiopathic arthritis - perforinopathy: case based review.

Pulmonary thromboendarterectomy in pediatric patients: Report of three cases.

Father`s role in infantile anorexia.

Meconium periorchitis: An incidentally diagnosed rare entity during inguinal herniorraphy.

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