The Turkish Journal of Pediatrics
Smilar Issues: 21 Record Found
Evaluation of soluble transferring receptor levels in children with iron deficiency and beta thalassemia trait, and in newborns and their mothers Abstract Similar Articles Mail to Editor Neutrophil hypersegmentation and thrombocytosis in children with iron deficiency anemia Abstract Similar Articles Mail to Editor Does maternal iron supplementation during the lactation period affect iron status of exclusively breast-fed infants? Abstract Similar Articles Mail to Editor Effects of iron deficiency versus iron deficiency anemia on brainstem auditory evoked potentials in infancy Abstract Similar Articles Mail to Editor Plummer-Vinson Syndrome in a 15-Year-Old Boy Abstract Similar Articles Mail to Editor A rare cause of mental motor retardation: recessive congenital methemoglobinemia type II Abstract Similar Articles Mail to Editor Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 gene Abstract Similar Articles Mail to Editor Interactions between exhaled CO, smoking status and nicotine dependency in a sample of Turkish adolescents Abstract Similar Articles Mail to Editor Factors affecting onset of puberty in Denizli province in Turkey Abstract Similar Articles Mail to Editor Seasonal and gender differences in hemoglobin value in infants at 5-7 months of age Abstract Similar Articles Mail to Editor Maternal and Environmental Determinants of Breast-Milk Mercury Concentrations Abstract Similar Articles Mail to Editor A Community-Based Iron Supplementation Program, “Iron-Like Turkey”, and the Following Prevalence of Anemia among Infants Aged 12-23 Months Abstract Similar Articles Mail to Editor Iron deficiency anemia in late-preterm infants Abstract Similar Articles Mail to Editor Severe Iron Deficiency Anemia and Marked Eosinophilia in Adolescent Girls with the Diagnosis of Human Fascioliasis Abstract Similar Articles Mail to Editor “Silent” β-thalassemia mutation (promoter nt-101 C > T) with increased hemoglobin A2 Abstract Similar Articles Mail to Editor Recessive congenital methemoglobinemia in immediate generations Abstract Similar Articles Mail to Editor Investigation of the frequency of iron insufficiency among infants in a population in which routine iron supplementation is implemented Abstract Similar Articles Mail to Editor Speech delay in toddlers: Are they only `late talkers`? Abstract Similar Articles Mail to Editor Chelation therapy for secondary neonatal iron over load: Lessons learned from rhesus hemolytic disease Abstract Similar Articles Mail to Editor Sustained hyperferritinemia in a child with macrophage activation syndrome secondary to systemic juvenile idiopathic arthritis - perforinopathy: case based review Abstract Similar Articles Mail to Editor Severe iron deficiency anemia and anasarca edema due to excessive cow`s milk intake Abstract Similar Articles Mail to Editor
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