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The Turkish Journal of Pediatrics 2003 , Vol 45 , Num 3
Letter to Editor
Original Article
Tropical pediatrics: 2002 to 2015 Abstract Full Text:PDF Similar Articles Molecular analysis of neurofibromatosis type 1 in Turkish families using polymorphic markers Abstract Full Text:PDF Similar Articles Analysis of the modifying effects of SAA1, SAA2 and TNF-alpha gene polymorphisms on development of amyloidosis in FMF patients Abstract Full Text:PDF Similar Articles Impact of migration on helicobacter pylori seroprevalence in the offspring of Turkish immigrants in Germany Abstract Full Text:PDF Similar Articles The results of electrophysiological study and radiofrequency catheter ablation in pediatric patients with tachyarrhythmia Abstract Full Text:PDF Similar Articles Congenital cardiac defects with 22q11 deletion Abstract Full Text:PDF Similar Articles Clinical, electrophysiological and neuropsychological findings of twenty-two children with mesial temporal sclerosis Abstract Full Text:PDF Similar Articles Association between early childhood caries and clinical, microbiological, oral hygiene and dietary variables in rural Turkish children Abstract Full Text:PDF Similar Articles Clinical analysis of the trigger thumb of childhood Abstract Full Text:PDF Similar Articles Evaluation of bone with quantitative ultrasound in healthy Turkish children Abstract Full Text:PDF Similar Articles
Case Report
Topical N-acetylcysteine treatment in neonatal ichthyosis Abstract Full Text:PDF Similar Articles Successful medical management of neutropenic enterocolitis (typhlitis) in a child with acute lymphoblastic leukemia Abstract Full Text:PDF Similar Articles Childhood lichen planus with nail involvement: a case Abstract Full Text:PDF Similar Articles Endobronchial tuberculosis complicated with staphylococcus aureus pneumonia and empyema in a child Abstract Full Text:PDF Similar Articles A rare cause of protein-losing enteropathy and growth retardation in infancy: infantile systemic hyalinosis Abstract Full Text:PDF Similar Articles A case of hereditary angioedema with recurrent arthritis, erythema marginatum-like rash and chest pain Abstract Full Text:PDF Similar Articles Congetial cutis laxa syndrome: type II autosomal recessive inheritance Abstract Full Text:PDF Similar Articles Persistent elevated serum levels of intact parathyroid hormone after reoperation for primary hyperparathyroidism and after pamidronate therapy Abstract Full Text:PDF Similar Articles Bardet-Biedl syndrome associated with vaginal atresia: a case report Abstract Full Text:PDF Similar Articles Sacrococcygeal extraspinal ependymoma: a case report Abstract Full Text:PDF Similar Articles
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