Volume 42 Issue 3 (2000)

Published: September 28, 2000

Original Articles

Polymorphisms of surfactant protein A genes and the risk of bronchopulmonary dysplasia in preterm infants
Dual-probe pH monitoring for the assessment of gastroesophageal reflux in the course of chronic hoarseness in children
Allogeneic bone marrow transplantation for children with myelodysplastic syndrome
Fludarabine, cytarabine, G-CSF and idarubicin (FLAG-IDA) for the treatment of relapsed or poor risk childhood acute leukemia
Hemophilic arthropathy: evaluation of clinical and radiological characteristics and disability
Clinical features of 21 patients with lissencephaly type I (agyria-pachygyria)
Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations
Serratia marcescens: an emerging microorganism in the neonatal intensive care unit
Ventricular diastolic filling indices in pulmonary stenosis
Unguarded tricuspid orifice diagnosed by echocardiography: a clinical study

Case Reports

Hereditary angioedema: case report of a family
Ivemark syndrome: asplenia with kidney collecting duct cysts and polysplenia with cerebellar cyst
A case of isotretinoin embryopathy with bilateral anotia and Taussig-Bing malformation
Teratoid Wilms' tumor: a case report
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome) in a Turkish child
Body stalk anomaly in monozygotic twinning: a case report
Thoracic ectopic kidney in a child: a case report
Acute lymphoblastic leukemia in a child with Wilson disease
Biphasic pulmonary blastoma in a child
Juvenile hyaline fibromatosis in one Turkish child

Letters to the Editor

Leukocytoclastic vasculitis associated with methotrexate therapy
Concurrent presence of HBsAg and anti-HBs in children