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The Turkish Journal of Pediatrics 2019 , Vol 61 , Num 3
Original Article
Thirty years of the newborn screening program in Central Serbia: the missed cases of congenital hypothyroidism Abstract Full Text:PDF Similar Articles Mail to Author Infant lymphoblastic leukemia: a single centers 10 year experience Abstract Full Text:PDF Similar Articles Mail to Author Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations Abstract Full Text:PDF Similar Articles Mail to Author Comparison of neonatal reference intervals for 23 biochemical analytes in the cord blood-A single center study in South Korea Abstract Full Text:PDF Similar Articles Mail to Author The relationships between nomophobia, alexithymia and metacognitive problems in an adolescent population Abstract Full Text:PDF Similar Articles Mail to Author Nitrogen balance of very preterm infants with extrauterine growth restriction Abstract Full Text:PDF Similar Articles Mail to Author 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 Abstract Full Text:PDF Similar Articles Mail to Author Clinical features and laboratory findings in children hospitalized with acute Epstein-Barr virus infection: a crosssectional study in a tertiary care hospital Abstract Full Text:PDF Similar Articles Mail to Author Comparison between the motor function of school-aged children with normal birth weight and children with low birth weight: a cross-sectional study Abstract Full Text:PDF Similar Articles Mail to Author Chronic recurrent multifocal osteomyelitis in children: a single center experience over five years Abstract Full Text:PDF Similar Articles Mail to Author The effects of enteral artificial amniotic fluid-containing erythropoietin on short term outcomes of preterm infants Abstract Full Text:PDF Similar Articles Mail to Author Correlation of the Bayley scales of infant-toddler development-3rd edition and neuro-sensory motor assessment in preterm infants during the first year of life. Abstract Full Text:PDF Similar Articles Mail to Author Outcome of allogeneic Hematopoietic Stem Cell Transplantation on Diamond-Blackfan anemia using busulfan-based myeloablative regimen Abstract Full Text:PDF Similar Articles Mail to Author
Case Report
Atypical phenotype of an old disease or typical phenotype of a new disease: deficiency of adenosine deaminase 2 Abstract Full Text:PDF Similar Articles Mail to Author Thrombotic thrombocytopenic purpura as a rare cause of anemia with thrombocytopenia in childhood: report of 2 cases Abstract Full Text:PDF Similar Articles Mail to Author IPEX syndrome: an easily-missed diagnosis of a life threatening condition Abstract Full Text:PDF Similar Articles Mail to Author Charcot-Marie-Tooth 1A concurrent with anaplastic ependymoma in a toddler: when an acute event unmasks a chronic condition Abstract Full Text:PDF Similar Articles Mail to Author A rare cause of vomiting in an adolescent: gastric Burkitt`s lymphoma Abstract Full Text:PDF Similar Articles Mail to Author Excision of the atrial Wilms` tumor thrombus without sternotomy, atriotomy and cardiovascular By-pass Abstract Full Text:PDF Similar Articles Mail to Author Exercise-induced anaphylaxis: a case report and review of the literature Abstract Full Text:PDF Similar Articles Mail to Author Concomitance of Familial Mediterranean Fever and Gitelman syndrome in an adolescent Abstract Full Text:PDF Similar Articles Mail to Author Coexistence or a related condition: an infant with retinoblastoma and Gaucher disease Abstract Full Text:PDF Similar Articles Mail to Author Acute ischemic stroke following water immersion seizure: a case report Abstract Full Text:PDF Similar Articles Mail to Author A synchronous occurrence of bifocal intracranial germinoma and bilateral testicular epidermoid cyst in an adolescent patient with Klinefelter`s syndrome Abstract Full Text:PDF Similar Articles Mail to Author Perforation of Meckel`s diverticulum in a very low birth weight neonate with severe pneumoperitoneum and review of literature Abstract Full Text:PDF Similar Articles Mail to Author
Short Report
A novel evaluation of genetic polymorphism in BCG adenitis Abstract Full Text:PDF Similar Articles Mail to Author
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