TURKISH JOURNAL OF PEDIATRICS

Acute lymphoblastic leukemia presenting as nephromegaly in a child: A rare case report.

Comparison between the motor function of school-aged children with normal birth weight and children with low birth weight: a cross-sectional study.

Clinical, electrophysiological findings and evaluation of prognosis of patients with Guillain-Barré syndrome.

Hemophagocytic lymphohistiocytosis associated with oxcarbazepine.

The effects of enteral artificial amniotic fluid-containing erythropoietin on short term outcomes of preterm infants.

A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism.

Acute ophthalmoparesis and persistent mydriasis: expanding the clinical spectrum of anti-GQ1b positive cranial neuropathy in a 5.5-year-old girl.

Body mass index is decreased in children and adolescents with postural tachycardia syndrome.

An infant with intradural extramedullary synovial sarcoma: the youngest case in the literature.

The relationships between nomophobia, alexithymia and metacognitive problems in an adolescent population.

Coexistence or a related condition: an infant with retinoblastoma and Gaucher disease.

A rare cause of vomiting in an adolescent: gastric Burkitt`s lymphoma.

Chronic recurrent multifocal osteomyelitis in children: a single center experience over five years.

The pathogens and curative effects analysis of perianal abscess of infants under 3 months.

The impact of 21-hydroxylase deficiency on cardiac repolarization changes in children with 21-hydroxylasedeficient congenital adrenal hyperplasia.

Cigarette smoking in adolescents with type 1 diabetes mellitus and congenital adrenal hyperplasia.

From Uganda to Italy: a case of nephrotic syndrome secondary to Plasmodium infection, Quartan malarial nephropathy and kidney failure.

Impact of the mandatory Hepatitis A immunization program: before and after the vaccine in Ankara, Central of Turkey.

Exercise-induced anaphylaxis: a case report and review of the literature.

Atypical phenotype of an old disease or typical phenotype of a new disease: deficiency of adenosine deaminase 2.

Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations.

Is serum procalcitonin level a reliable indicator in early diagnosis of congenital pneumonia?

Impacts of phototherapy on DNA damage and total oxidant/ antioxidant status in jaundiced newborns.

Severe iron deficiency anemia and anasarca edema due to excessive cow`s milk intake.

Reliability and validity of the pediatric feeding and swallowing disorders family impact scale for Turkish children with cerebral palsy by endoscopic evaluation.

Pulmonary complications following hematopoietic stem cell transplantation in children.

Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis.

Hematological disturbances in Down syndrome: single centre experience of thirteen years and review of the literature.

Concomitance of Familial Mediterranean Fever and Gitelman syndrome in an adolescent.

Familial reciprocal non robertsonian translocation t(14;22) resulting in 22q11.2 deletion syndrome.

Congenital long-QT syndrome in type 1 diabetes: a unique association.

Early onset inflammatory bowel disease: manifestations, genetics and diagnosis.

The effectiveness of serum amyloid A for prediction of neonatal cholestasis associated with parenteral nutrition in premature infants.

Etiology of vaginal discharge in sexually inactive adolescents.

An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment.

Vedolizumab treatment in a patient with X-linked agammaglobulinemia, is it safe and efficient?

Comparison of neonatal reference intervals for 23 biochemical analytes in the cord blood-A single center study in South Korea.

Neonatal form of biotin-thiamine-responsive basal ganglia disease. Clues to diagnosis.

Thirty years of the newborn screening program in Central Serbia: the missed cases of congenital hypothyroidism.

The predictive value of procalcitonin, C-reactive protein, presepsin, and soluble-triggering receptor expressed on myeloid cell levels in bloodstream infections in pediatric patients with febrile neutropenia.

Fetal intrapericardial teratomas.

Excision of the atrial Wilms` tumor thrombus without sternotomy, atriotomy and cardiovascular By-pass.

Syncope due to acute rheumatic fever with pacemaker-like syndrome.

Infant lymphoblastic leukemia: a single centers 10 year experience.

IPEX syndrome: an easily-missed diagnosis of a life threatening condition.

Does stable sitting influence upper limb function in children with cerebral palsy?

Two years of newborn screening for cystic fibrosis in Turkey: Çukurova experience.