The Turkish Journal of Pediatrics
2022 , Vol 64 , Num 5
Quality of life and the psychological status of the adolescents with asthma and their parents during the COVID-19 pandemic.
The relationship between smoking, alcohol, and substance abuse and psychiatric diseases among adolescents treated in a child and adolescent psychiatry inpatient unit.
Phenotypic and genotypic characteristics of children with Bartter syndrome.
Complicated acute appendicitis in children: the importance of stewarding antibiotic prescriptions.
Clinical findings of methicillin-resistant Staphylococcus aureus in cystic fibrosis.
Comparison of miRNA expression in patients with seasonal and perennial allergic rhinitis and non-atopic asthma.
Pedipacks in the transfusion of pediatric patients to reduce wastage of blood components: an observational study from a tertiary center.
Decreased antioxidant capacity with serum native thiol and total thiol levels in children with hemophilia A: a prospective case-control study.
Imaging spectrum of extracorporeal membrane oxygenation related neurologic events in children.
Hyperprolactinemia in children and adolescents and longterm follow-up results of prolactinoma cases: a single-centre experience.
Clinical course of primary empty sella in children: a singlecenter experience.
Intrathyroidal ectopic thymus: an important entity in the differential diagnosis of thyroid nodules.
Cyclopentolate eye drops-induced anaphylaxis in an infant.
Severe acute kidney injury induced by crescentic glomerulonephritis in a child with infective endocarditis.
3q29 microdeletion syndrome associated with developmental delay and pulmonary stenosis: a case report.
The anomalous drainage of the inferior vena cava into the left atrium.
A unique case of a newborn with a hemangioma on the omphalocele sac.
Giant cell tumor arising from the anterior arc of the rib: an extremely rare site in an adolescent girl.
Persistent moderate methylmalonic aciduria in a patient with methylmalonyl CoA epimerase deficiency.
Pyruvate kinase deficiency mimicking congenital dyserythropoietic anemia type I.
Three Afghani siblings with a novel homozygous variant and further delineation of the clinical features of METTL5 related intellectual disability syndrome.
A child presenting with bullous emphysema.
The relationship between smoking, alcohol, and substance abuse and psychiatric diseases among adolescents treated in a child and adolescent psychiatry inpatient unit.
Phenotypic and genotypic characteristics of children with Bartter syndrome.
Complicated acute appendicitis in children: the importance of stewarding antibiotic prescriptions.
Clinical findings of methicillin-resistant Staphylococcus aureus in cystic fibrosis.
Comparison of miRNA expression in patients with seasonal and perennial allergic rhinitis and non-atopic asthma.
Pedipacks in the transfusion of pediatric patients to reduce wastage of blood components: an observational study from a tertiary center.
Decreased antioxidant capacity with serum native thiol and total thiol levels in children with hemophilia A: a prospective case-control study.
Imaging spectrum of extracorporeal membrane oxygenation related neurologic events in children.
Hyperprolactinemia in children and adolescents and longterm follow-up results of prolactinoma cases: a single-centre experience.
Clinical course of primary empty sella in children: a singlecenter experience.
Intrathyroidal ectopic thymus: an important entity in the differential diagnosis of thyroid nodules.
Cyclopentolate eye drops-induced anaphylaxis in an infant.
Severe acute kidney injury induced by crescentic glomerulonephritis in a child with infective endocarditis.
3q29 microdeletion syndrome associated with developmental delay and pulmonary stenosis: a case report.
The anomalous drainage of the inferior vena cava into the left atrium.
A unique case of a newborn with a hemangioma on the omphalocele sac.
Giant cell tumor arising from the anterior arc of the rib: an extremely rare site in an adolescent girl.
Persistent moderate methylmalonic aciduria in a patient with methylmalonyl CoA epimerase deficiency.
Pyruvate kinase deficiency mimicking congenital dyserythropoietic anemia type I.
Three Afghani siblings with a novel homozygous variant and further delineation of the clinical features of METTL5 related intellectual disability syndrome.
A child presenting with bullous emphysema.