The Turkish Journal of Pediatrics
Smilar Issues: 33 Record Found
Achondroplasia in Turkey is defined by recurrent G380R mutation of the FGFR3 gene Abstract Similar Articles Mail to Editor A rare cause of protein-losing enteropathy and growth retardation in infancy: infantile systemic hyalinosis Abstract Similar Articles Mail to Editor Influence of iodine supplementation on serum insulin-like growth factor-I (IGF-I) and IGF-binding protein-3 (IGFBP-3) levels in severe iodine deficiency Abstract Similar Articles Mail to Editor Progression to renal failure Abstract Similar Articles Mail to Editor Growth and nutrition of children with chronic renal failure Abstract Similar Articles Mail to Editor Long-term enteral glutamine supplementation in very low birth weight infants: effects on growth parameters Abstract Similar Articles Mail to Editor Correlation between vascular endothelial growth factor and leptin in children with cyanotic congenital heart disease Abstract Similar Articles Mail to Editor Factors affecting onset of puberty in Denizli province in Turkey Abstract Similar Articles Mail to Editor Catch-up growth in appropriate- or small-for-gestational age preterm infants Abstract Similar Articles Mail to Editor Somatic growth after corrective surgery for congenital heart disease Abstract Similar Articles Mail to Editor Growth Hormone Deficiency Due to Traumatic Brain Injury in a Patient with X-linked Congenital Adrenal Hypoplasia Abstract Similar Articles Mail to Editor Fetal arterial and venous Doppler in growth restricted fetuses for the prediction of perinatal complications Abstract Similar Articles Mail to Editor Weight, Height and BMI References in Elazığ: An East Anatolian City Abstract Similar Articles Mail to Editor A Rare Case of 2q37 Microdeletion with Albright Hereditary Osteodystrophy-Like Phenotype Abstract Similar Articles Mail to Editor Transforming Growth Factor-Beta1 (509 C/T, 915 G/C, 869 T/C) Polymorphisms Are Not Related to Obesity in Turkish Children Abstract Similar Articles Mail to Editor A Study of Growth Failure and its Related Factors in Children from 0 to 2 Years in Tehran, Iran Abstract Similar Articles Mail to Editor Family and Infant Characteristics in Relation to Age at Walking in Turkey Abstract Similar Articles Mail to Editor Frequency of Mutations in PROP-1 Gene in Turkish Children with Combined Pituitary Hormone Deficiency Abstract Similar Articles Mail to Editor Renal Function and Linear Growth of Children with Nephrocalcinosis: A Retrospective Single-Center Study Abstract Similar Articles Mail to Editor Short- and Long-Term Effects of Individualized Enteral Protein Supplementation in Preterm Newborns Abstract Similar Articles Mail to Editor Assessing Leptin and Soluble Leptin Receptor Levels in Full-Term Asymmetric Small for Gestational Age and Healthy Neonates Abstract Similar Articles Mail to Editor Determinants of Continued Breastfeeding beyond 12 Months in Turkey: Secondary Data Analysis of the Demographic and Health Survey Abstract Similar Articles Mail to Editor The effect of growth hormone treatment on head circumference in growth hormone-deficient children Abstract Similar Articles Mail to Editor Adult height in Turkish patients with Turner syndrome without growth hormone treatment Abstract Similar Articles Mail to Editor Perinatal features and umbilical cord blood gases in newborns complicated with nuchal cord Abstract Similar Articles Mail to Editor Novel Nonsense Mutation of GPC3 Gene in a Patient with Simpson-Golabi-Behmel Syndrome Abstract Similar Articles Mail to Editor Neuroendocrine Immune System in Familial Mediterranean Fever Abstract Similar Articles Mail to Editor An Aggressive Parenteral Nutrition Protocol Improves Growth in Preterm Infants Abstract Similar Articles Mail to Editor Platelets and Platelet-Derived Growth Factor in Closure of the Ductus Arteriosus Abstract Similar Articles Mail to Editor Horseshoe kidney with growth retardation: Don’t forget Turner syndrome Abstract Similar Articles Mail to Editor Aggressive periodontitis associated with Kindler syndrome in a large Kindler syndrome pedigree Abstract Similar Articles Mail to Editor Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome Abstract Similar Articles Mail to Editor Changes in trajectories of physical growth in a domestic adoptees sample: A preliminary study Abstract Similar Articles Mail to Editor
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