The Turkish Journal of Pediatrics
Smilar Issues: 76 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 Serum leptin levels in patients with 21-hydroxylase deficiency before and after treatment Abstract Similar Articles Mail to Editor A case of hereditary angioedema with recurrent arthritis, erythema marginatum-like rash and chest pain Abstract Similar Articles Mail to Editor Back to the basics: hemorrhage after vaccination: a case report Abstract Similar Articles Mail to Editor Assessment of goiter prevalence, iodine status and thyroid functions in school-age children of rural Yusufeli district in eastern Turkey Abstract Similar Articles Mail to Editor A newborn infant with generalized glutathione synthetase deficiency 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 Triple-X syndrome accompanied by congenital adrenal hyperplasia: case report Abstract Similar Articles Mail to Editor A case with ICF syndrome lost to rubella pneumonitis Abstract Similar Articles Mail to Editor Neutrophil hypersegmentation and thrombocytosis in children with iron deficiency anemia Abstract Similar Articles Mail to Editor Urinary tract infection and hyperbilirubinemia 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 Cholestatic hepatitis as a result of severe cortisol deficiency in early infancy: report of two cases and review of literature Abstract Similar Articles Mail to Editor A case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomalies Abstract Similar Articles Mail to Editor Acetaminophen-induced hepatotoxicity in a glutathione synthetase-deficient patient Abstract Similar Articles Mail to Editor Genetic factors in neonatal hyperbilirubinemia and kernicterus Abstract Similar Articles Mail to Editor Peripheral blood lymphocyte subsets in children with frequent upper respiratory tract infections Abstract Similar Articles Mail to Editor Mild Clinical Phenotype and Subtle Radiographic Findings in an Infant with Cartilage-Hair Hypoplasia Abstract Similar Articles Mail to Editor Plummer-Vinson Syndrome in a 15-Year-Old Boy Abstract Similar Articles Mail to Editor Early and severe presentation of vitamin D deficiency and nutritional rickets among hospitalized infants and the effective factors Abstract Similar Articles Mail to Editor 3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures Abstract Similar Articles Mail to Editor Neurologic findings of nutritional vitamin B12 deficiency in children Abstract Similar Articles Mail to Editor Common variable immunodeficiency: familial inheritance and autoimmune manifestations in two siblings Abstract Similar Articles Mail to Editor Pediatric cardiac surgery under cardiopulmonary bypass in factor VII deficiency Abstract Similar Articles Mail to Editor Is neonatal antiretroviral therapy a risk factor for NEC occurrence? Abstract Similar Articles Mail to Editor The Etiology of Severe Neonatal Hyperbilirubinemia and Complications of Exchange Transfusion Abstract Similar Articles Mail to Editor Hereditary C1q Deficiency: A New Family with C1qA Deficiency 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 Primary immune deficiency disease awareness among a group of Turkish physicians Abstract Similar Articles Mail to Editor Is Basal Serum 17-OH Progesterone A Reliable Parameter To Predict Nonclassical Congenital Adrenal Hyperplasia in Premature Adrenarche? Abstract Similar Articles Mail to Editor Disseminated BCG as A Unique Feature of An Infant with Severe Combined Immunodeficiency Abstract Similar Articles Mail to Editor Vitamin D-Deficient Rickets Mimicking Ankylosing Spondylitis in an Adolescent Girl Abstract Similar Articles Mail to Editor Neonatal Exchange Transfusion for Hyperbilirubinemia in Guilan (The North Province of Iran): A 3-Year Experience Abstract Similar Articles Mail to Editor Mevalonate Kinase Deficiency (Hyper IgD Syndrome with Periodic Fever) - Different Faces with Separate Treatments: Two Cases and Review of the Literature Abstract Similar Articles Mail to Editor Comparison of Intensive Light-Emitting Diode and Intensive Compact Fluorescent Phototherapy in Non-Hemolytic Jaundice Abstract Similar Articles Mail to Editor Mild Hemolytic Anemia, Progressive Neuromotor Retardation and Fatal Outcome: A Disorder of Glycolysis, Triose- Phosphate Isomerase Deficiency Abstract Similar Articles Mail to Editor Salmonella Meningitis in a 16-Month-Old Child with AIDS Abstract Similar Articles Mail to Editor Allergic diseases in children with primary immunodeficiencies Abstract Similar Articles Mail to Editor Effect of Supplementary Zinc on Body Mass Index, Pulmonary Function and Hospitalization in Children with Cystic Fibrosis 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 Neonatal Multiple Sulfatase Deficiency with a Novel Mutation and Review of the Literature Abstract Similar Articles Mail to Editor Effects of Seasonal Variation and Maternal Clothing Style on Vitamin D Levels of Mothers and Their Infants Abstract Similar Articles Mail to Editor Composition of Parenteral Nutrition Solution Affects the Time of Occurrence But Not the Incidence of Cholestasis in Surgical Infants Abstract Similar Articles Mail to Editor Comparison of Transcutaneous and Total Serum Bilirubin Measurement in Turkish Newborns Abstract Similar Articles Mail to Editor Association between Vitamin D Deficiency and Disease Activity in Juvenile Idiopathic Arthritis 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 Ataxia with vitamin E deficiency associated with deafness Abstract Similar Articles Mail to Editor A rare cause of hyperbilirubinemia in a newborn: bilateral adrenal hematoma Abstract Similar Articles Mail to Editor A causal relationship between UDP-glucuronosyltransferase 1A1 promoter polymorphism and idiopathic hyperbilirubinemia in Turkish newborns Abstract Similar Articles Mail to Editor Exchange transfusion in severe hyperbilirubinemia: an experience in northwest Iran Abstract Similar Articles Mail to Editor Late Vitamin K Deficiency Bleeding in an Infant with Choledochal Cyst Abstract Similar Articles Mail to Editor Adrenal Bleeding İn Neonates: Report Of 37 Cases* Abstract Similar Articles Mail to Editor Glucose-6-Phosphate Dehydrogenase Activity, Structure, Molecular Characteristics and Role in Neonatal Hyperbilirubinemia in Cord Blood in Çukurova Region Abstract Similar Articles Mail to Editor Prevalence of Selective Immunoglobulin A Deficiency in Healthy Turkish School Children Abstract Similar Articles Mail to Editor Hypocalcemic seizure in an adolescent with Down syndrome: a manifestation of unrecognized celiac disease Abstract Similar Articles Mail to Editor An Easily Missed Diagnosis: 17-Alpha-Hydroxylase/17,20-Lyase Deficiency Abstract Similar Articles Mail to Editor Clinical and genetic features of IL12Rb1 deficiency: Single center experience of 18 patients Abstract Similar Articles Mail to Editor Infectious diseases, autoimmunity and midline defect in a patient with a novel bi-allelic mutation in IL12RB1 gene Abstract Similar Articles Mail to Editor Late-diagnosed phenylketonuria in an eight-year-old boy with dyslexia and attention-deficit hyperactivity disorder Abstract Similar Articles Mail to Editor Coexistence of early onset sarcoidosis and partial interferon-γ receptor 1 deficiency Abstract Similar Articles Mail to Editor Recognizing immunodeficiency in children with recurrent infections: What are the predictive factors? Abstract Similar Articles Mail to Editor Increasing vitamin D deficiency in children from 1995 to 2011 Abstract Similar Articles Mail to Editor Treatment of a patient with Kawasaki disease associated with selective IgA deficiency by continuous infusion of cyclosporine A without intravenous immunoglobulin Abstract Similar Articles Mail to Editor A case report of a 4-year-old child with glucose-6-phosphate dehydrogenase deficiency: An evidence based approach to nutritional management Abstract Similar Articles Mail to Editor p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency Abstract Similar Articles Mail to Editor Is there clinical value in counting nucleated red blood cells and platelet indices in primary immunodeficiency disease? 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 Advantage of the subcutaneous immunoglobulin replacement therapy in primary immunodeficient patients with or without secondary protein loss Abstract Similar Articles Mail to Editor Folate deficiency in patients with classical galactosemia: A novel finding that needs to be considered for dietary treatments Abstract Similar Articles Mail to Editor Effects of Lactobacillus rhamnosus GG as a probiotic on neonatal hyperbilirubinemia Abstract Similar Articles Mail to Editor Asymptomatic intracranial hemorrhage in a newborn with congenital factor VII deficiency and successful treatment with recombinant activated factor VII Abstract Similar Articles Mail to Editor Coexistence of 2 rare autosomal recessively inherited disorders manifesting with immune deficiency; IL-12 receptor β1 and biotinidase deficiencies Abstract Similar Articles Mail to Editor A novel mutation of interleukin-1 receptor antagonist (IL1RN) in a DIRA patient from Turkey: Diagnosis and treatment Abstract Similar Articles Mail to Editor A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism 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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