The Turkish Journal of Pediatrics
Smilar Issues: 128 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 Interobserver reliability of articular examination in juvenile idiopathic arthritis 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 The results of electrophysiological study and radiofrequency catheter ablation in pediatric patients with tachyarrhythmia 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 Maternal vitamin D deficiency and vitamin D supplementation in healthy infants Abstract Similar Articles Mail to Editor The effect of vitamin D3 on CD34 progenitor cells in vitamin D deficiency rickets 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 Vertebra and femur neck bone mineral density values in healthy Turkish children 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 Comorbid psychiatric disorders in 201 cases of encopresis 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 Childhood acute rheumatic fever in Ankara, Turkey Abstract Similar Articles Mail to Editor Blood lead levels of maternal-cord pairs, children and adults who live in a central urban area in Turkey Abstract Similar Articles Mail to Editor Neutrophil hypersegmentation and thrombocytosis in children with iron deficiency anemia Abstract Similar Articles Mail to Editor Use of alendronate in the treatment of vitamin D intoxication in infants Abstract Similar Articles Mail to Editor Concurrent septic arthritis and urinary tract infection in a patient with nephrocalcinosis and vesicoureteral reflux 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 Hypocalcemic seizure due to congenital rickets in the first day of life Abstract Similar Articles Mail to Editor Vitamin D receptor gene polymorphisms in Turkish children with vitamin D deficient rickets 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 Hypertension in Children (12–14 Years) – A Case–Control Study in Bursa, Turkey Abstract Similar Articles Mail to Editor Validation and Reliability Study of the Turkish Version of the Pediatric Rhinitis Quality of Life Questionnaire Abstract Similar Articles Mail to Editor Plummer-Vinson Syndrome in a 15-Year-Old Boy Abstract Similar Articles Mail to Editor Estimated daily intake of cadmium by children living in the city of Niš, Serbia Abstract Similar Articles Mail to Editor Exposure to house dust endotoxin and allergic sensitization in allergic and nonallergic children living in Adana, Turkey 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 Acquired partial lipodystrophy associated with varicella 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 Visceral Larva Migrans Among Children in Kütahya (Turkey) and an Evaluation of Playgrounds for T. canis Eggs Abstract Similar Articles Mail to Editor Hereditary C1q Deficiency: A New Family with C1qA Deficiency Abstract Similar Articles Mail to Editor The Presentation of Celiac Disease in 220 Turkish Children 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 Cardiovascular Findings İn A Boy With Arterial Tortuosity Syndrome: Case Report And Review Of The Literature 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 Atypical Presentation of Antrochoanal Polyp in A Child 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 Meningococcal Disease in Children: A Clinical Review Abstract Similar Articles Mail to Editor The Levels of Asymmetric Dimethylarginine, Homocysteine and Carotid Intima-Media Thickness in Hypercholesterolemic Children Abstract Similar Articles Mail to Editor A Study of the Prevalence of Developmental Anomalies of the External Ear among Preschool Children in Sivas, Turkey Abstract Similar Articles Mail to Editor Helicobacter pylori Infection and Peptic Ulcer in Eastern Turkish Children: Is It More Common than Known? Abstract Similar Articles Mail to Editor Assessment of Bone Density in Children with Cerebral Palsy by Areal Bone Mineral Density Measurement Abstract Similar Articles Mail to Editor Albendazole-Induced Dystonic Reaction: A Case Report Abstract Similar Articles Mail to Editor Vitamin D Intoxication Abstract Similar Articles Mail to Editor Tularemia in Children: Evaluation of Clinical, Laboratory and Therapeutic Features of 27 Tularemia Cases Abstract Similar Articles Mail to Editor Vitamin D-Deficient Rickets Mimicking Ankylosing Spondylitis in an Adolescent Girl Abstract Similar Articles Mail to Editor Hypohidrosis and Hyperthermia during Topiramate Treatment in Children Abstract Similar Articles Mail to Editor Takayasu Arteritis in a 4-Year-Old Girl: Case Report and Brief Overview of the Pediatric Literature Abstract Similar Articles Mail to Editor Fever of Unknown Origin in Children: The Experience of One Center in Turkey 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 Transient Acute Flaccid Paralysis and Seizures Associated with Rotavirus Gastroenteritis in a Child Abstract Similar Articles Mail to Editor An Unusual Cause of Secondary Capillary Leak Syndrome in a Child: Rotavirus Diarrhea 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 Oral Findings and Clinical Implications of Patients with Congenital Neutropenia: A Literature Review Abstract Similar Articles Mail to Editor Acute Disseminated Encephalomyelitis: An Evaluation of 15 Cases in Childhood Abstract Similar Articles Mail to Editor Neurophysiological Follow-Up of Two Siblings with Crigler-Najjar Syndrome Type I and Review of Literature Abstract Similar Articles Mail to Editor Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report Abstract Similar Articles Mail to Editor Usefulness of long-term video-EEG monitoring in children at a tertiary care center Abstract Similar Articles Mail to Editor Allergic diseases in children with primary immunodeficiencies Abstract Similar Articles Mail to Editor Acute tubulointerstitial nephritis-uveitis (TINU) syndrome developed secondary to paracetamol and codeine phosphate use: two case reports Abstract Similar Articles Mail to Editor Successful noninvasive mechanical ventilation in a child on prolonged and life-threatening invasive mechanical ventilation after Fontan operation 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 Erythema Nodosum in Children: Evaluation of 39 Patients Abstract Similar Articles Mail to Editor Enterobius Granuloma: An Unusual Cause of Omental Mass in an 11-Year-Old Girl Abstract Similar Articles Mail to Editor A Rare Cause of Abdominal Lymphadenopathy – Tularemia: Report of Two Pediatric Cases 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 Psoas Abscess with Septic Arthritis of the Hip: A Case Report Abstract Similar Articles Mail to Editor Molecular Epidemiology and Antibiotic Susceptibility Pattern of Acinetobacter baumannii Isolated from Children in a Turkish University Hospital 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 Neuroleptic Malignant Syndrome Associated with Metoclopramide in a Child Abstract Similar Articles Mail to Editor Association between Vitamin D Deficiency and Disease Activity in Juvenile Idiopathic Arthritis Abstract Similar Articles Mail to Editor Primary Laryngeal Lymphoma in a Child Abstract Similar Articles Mail to Editor A Presentation of Lyme Disease: Pseudotumor Cerebri. 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 The frequency of autoimmune thyroid disorders in juvenile idiopathic arthritis Abstract Similar Articles Mail to Editor Ataxia with vitamin E deficiency associated with deafness 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 Treatment results of chronic hepatitis B in children: a retrospective study Abstract Similar Articles Mail to Editor Late Vitamin K Deficiency Bleeding in an Infant with Choledochal Cyst Abstract Similar Articles Mail to Editor Primary Epstein-Barr Virus Infection in 2-Year-Old Children: Report of 3 Cases Abstract Similar Articles Mail to Editor Evaluation Of Sixteen Children With Pseudotumor Cerebri 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 A Rare Tumor of Nasal Bone in a Child: Osteoblastoma Abstract Similar Articles Mail to Editor Prevalence of Selective Immunoglobulin A Deficiency in Healthy Turkish School Children Abstract Similar Articles Mail to Editor Impact of Maternal Vitamin D Status during Pregnancy on Neonatal Vitamin D Status Abstract Similar Articles Mail to Editor Acute Cerebellar Ataxia associated with Enteric Fever in a Child: A Case Report Abstract Similar Articles Mail to Editor Posterior Reversible Encephalopathy Syndrome due to Pulse Methylprednisolone Therapy in a Child 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 Intractable Colitis Associated with Chronic Granulomatous Disease in Young Girl 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 Serum vitamin D levels during activation and remission periods of patients with juvenile idiopathic arthritis and familial Mediterranean fever 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 Predictors of methotrexate response in Turkish children with oligoarticular and polyarticular juvenile idiopathic arthritis 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 Systems-level analysis of genome wide association study results for a pilot juvenile idiopathic arthritis family study Abstract Similar Articles Mail to Editor Vitamin D receptor gene polymorphisms in children with kidney stone disease Abstract Similar Articles Mail to Editor Subtype frequencies, demographic features, and remission rates in juvenile idiopathic arthritis – 265 cases from a Turkish center 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 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 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 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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