The Turkish Journal of Pediatrics
Smilar Issues: 163 Record Found
Evaluation of soluble transferring receptor levels in children with iron deficiency and beta thalassemia trait, and in newborns and their mothers
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Interobserver reliability of articular examination in juvenile idiopathic arthritis
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Serum leptin levels in patients with 21-hydroxylase deficiency before and after treatment
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The results of electrophysiological study and radiofrequency catheter ablation in pediatric patients with tachyarrhythmia
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A case of hereditary angioedema with recurrent arthritis, erythema marginatum-like rash and chest pain
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Maternal vitamin D deficiency and vitamin D supplementation in healthy infants
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The effect of vitamin D3 on CD34 progenitor cells in vitamin D deficiency rickets
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Back to the basics: hemorrhage after vaccination: a case report
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Assessment of goiter prevalence, iodine status and thyroid functions in school-age children of rural Yusufeli district in eastern Turkey
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A newborn infant with generalized glutathione synthetase deficiency
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Vertebra and femur neck bone mineral density values in healthy Turkish children
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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
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Comorbid psychiatric disorders in 201 cases of encopresis
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Triple-X syndrome accompanied by congenital adrenal hyperplasia: case report
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A case with ICF syndrome lost to rubella pneumonitis
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Childhood acute rheumatic fever in Ankara, Turkey
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Blood lead levels of maternal-cord pairs, children and adults who live in a central urban area in Turkey
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Neutrophil hypersegmentation and thrombocytosis in children with iron deficiency anemia
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Use of alendronate in the treatment of vitamin D intoxication in infants
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Concurrent septic arthritis and urinary tract infection in a patient with nephrocalcinosis and vesicoureteral reflux
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Does maternal iron supplementation during the lactation period affect iron status of exclusively breast-fed infants?
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Effects of iron deficiency versus iron deficiency anemia on brainstem auditory evoked potentials in infancy
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Cholestatic hepatitis as a result of severe cortisol deficiency in early infancy: report of two cases and review of literature
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A case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomalies
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Acetaminophen-induced hepatotoxicity in a glutathione synthetase-deficient patient
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Hypocalcemic seizure due to congenital rickets in the first day of life
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Vitamin D receptor gene polymorphisms in Turkish children with vitamin D deficient rickets
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Peripheral blood lymphocyte subsets in children with frequent upper respiratory tract infections
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Mild Clinical Phenotype and Subtle Radiographic Findings in an Infant with Cartilage-Hair Hypoplasia
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Hypertension in Children (12–14 Years) – A Case–Control Study in Bursa, Turkey
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Validation and Reliability Study of the Turkish Version
of the Pediatric Rhinitis Quality of Life Questionnaire
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Plummer-Vinson Syndrome in a 15-Year-Old Boy
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Estimated daily intake of cadmium by children living in the city of Niš, Serbia
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Exposure to house dust endotoxin and allergic sensitization in allergic and nonallergic children living in Adana, Turkey
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Early and severe presentation of vitamin D deficiency and nutritional rickets among hospitalized infants and the effective factors
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3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures
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Acquired partial lipodystrophy associated with varicella
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Neurologic findings of nutritional vitamin B12 deficiency in children
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Common variable immunodeficiency: familial inheritance and autoimmune manifestations in two siblings
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Pediatric cardiac surgery under cardiopulmonary bypass in factor VII deficiency
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Is neonatal antiretroviral therapy a risk factor for NEC occurrence?
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Visceral Larva Migrans Among Children in Kütahya (Turkey) and an Evaluation of Playgrounds for T. canis Eggs
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Hereditary C1q Deficiency: A New Family with C1qA Deficiency
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The Presentation of Celiac Disease in 220 Turkish Children
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Growth Hormone Deficiency Due to Traumatic Brain Injury in a Patient with X-linked Congenital Adrenal Hypoplasia
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Primary immune deficiency disease awareness among a group of Turkish physicians
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Cardiovascular Findings İn A Boy With Arterial Tortuosity Syndrome: Case Report And Review Of The Literature
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Is Basal Serum 17-OH Progesterone A Reliable Parameter To Predict Nonclassical Congenital Adrenal Hyperplasia in Premature Adrenarche?
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Atypical Presentation of Antrochoanal Polyp in A Child
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Disseminated BCG as A Unique Feature of An Infant with Severe Combined Immunodeficiency
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Meningococcal Disease in Children: A Clinical Review
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The Levels of Asymmetric Dimethylarginine, Homocysteine and Carotid Intima-Media Thickness in Hypercholesterolemic Children
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A Study of the Prevalence of Developmental Anomalies of the External Ear among Preschool Children in Sivas, Turkey
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Helicobacter pylori Infection and Peptic Ulcer in Eastern Turkish Children: Is It More Common than Known?
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Assessment of Bone Density in Children with Cerebral Palsy by Areal Bone Mineral Density Measurement
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Albendazole-Induced Dystonic Reaction: A Case Report
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Vitamin D Intoxication
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Tularemia in Children: Evaluation of Clinical, Laboratory and Therapeutic Features of 27 Tularemia Cases
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Vitamin D-Deficient Rickets Mimicking Ankylosing Spondylitis in an Adolescent Girl
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Hypohidrosis and Hyperthermia during Topiramate Treatment in Children
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Takayasu Arteritis in a 4-Year-Old Girl: Case Report and Brief Overview of the Pediatric Literature
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Fever of Unknown Origin in Children: The Experience of One Center in Turkey
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Mevalonate Kinase Deficiency (Hyper IgD Syndrome with Periodic Fever) - Different Faces with Separate Treatments: Two Cases and Review of the Literature
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Transient Acute Flaccid Paralysis and Seizures Associated with Rotavirus Gastroenteritis in a Child
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An Unusual Cause of Secondary Capillary Leak Syndrome in a Child: Rotavirus Diarrhea
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Mild Hemolytic Anemia, Progressive Neuromotor Retardation and Fatal Outcome: A Disorder of Glycolysis, Triose- Phosphate Isomerase Deficiency
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Salmonella Meningitis in a 16-Month-Old Child with AIDS
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Oral Findings and Clinical Implications of Patients with Congenital Neutropenia: A Literature Review
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Acute Disseminated Encephalomyelitis: An Evaluation of 15 Cases in Childhood
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Neurophysiological Follow-Up of Two Siblings with Crigler-Najjar Syndrome Type I and Review of Literature
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Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report
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Usefulness of long-term video-EEG monitoring in children at a tertiary care center
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Allergic diseases in children with primary immunodeficiencies
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Acute tubulointerstitial nephritis-uveitis (TINU) syndrome developed secondary to paracetamol and codeine phosphate use: two case reports
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Successful noninvasive mechanical ventilation in a child on prolonged and life-threatening invasive mechanical ventilation after Fontan operation
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Effect of Supplementary Zinc on Body Mass Index, Pulmonary Function and Hospitalization in Children with Cystic Fibrosis
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Erythema Nodosum in Children: Evaluation of 39 Patients
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Enterobius Granuloma: An Unusual Cause of Omental Mass in an 11-Year-Old Girl
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A Rare Cause of Abdominal Lymphadenopathy – Tularemia: Report of Two Pediatric Cases
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Severe Iron Deficiency Anemia and Marked Eosinophilia in Adolescent Girls with the Diagnosis of Human Fascioliasis
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Psoas Abscess with Septic Arthritis of the Hip: A Case Report
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Molecular Epidemiology and Antibiotic Susceptibility Pattern of Acinetobacter baumannii Isolated from Children in a Turkish University Hospital
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Neonatal Multiple Sulfatase Deficiency with a Novel Mutation and Review of the Literature
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Effects of Seasonal Variation and Maternal Clothing Style on Vitamin D Levels of Mothers and Their Infants
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Neuroleptic Malignant Syndrome Associated with Metoclopramide in a Child
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Association between Vitamin D Deficiency and Disease Activity in Juvenile Idiopathic Arthritis
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Primary Laryngeal Lymphoma in a Child
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A Presentation of Lyme Disease: Pseudotumor Cerebri.
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The effect of growth hormone treatment on head circumference in growth hormone-deficient children
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The frequency of autoimmune thyroid disorders in juvenile idiopathic arthritis
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Ataxia with vitamin E deficiency associated with deafness
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A causal relationship between UDP-glucuronosyltransferase 1A1 promoter polymorphism and idiopathic hyperbilirubinemia in Turkish newborns
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Treatment results of chronic hepatitis B in children: a retrospective study
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Late Vitamin K Deficiency Bleeding in an Infant with Choledochal Cyst
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Primary Epstein-Barr Virus Infection in 2-Year-Old Children: Report of 3 Cases
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Evaluation Of Sixteen Children With Pseudotumor Cerebri
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Glucose-6-Phosphate Dehydrogenase Activity, Structure, Molecular Characteristics and Role in Neonatal Hyperbilirubinemia in Cord Blood in Çukurova Region
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A Rare Tumor of Nasal Bone in a Child: Osteoblastoma
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Prevalence of Selective Immunoglobulin A Deficiency in Healthy Turkish School Children
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Impact of Maternal Vitamin D Status during Pregnancy on Neonatal Vitamin D Status
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Acute Cerebellar Ataxia associated with Enteric Fever in a Child: A Case Report
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Posterior Reversible Encephalopathy Syndrome due to Pulse Methylprednisolone Therapy in a Child
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Hypocalcemic seizure in an adolescent with Down syndrome: a manifestation of unrecognized celiac disease
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Intractable Colitis Associated with Chronic Granulomatous Disease in Young Girl
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An Easily Missed Diagnosis: 17-Alpha-Hydroxylase/17,20-Lyase Deficiency
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Clinical and genetic features of IL12Rb1 deficiency: Single center experience of 18 patients
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Infectious diseases, autoimmunity and midline defect in a patient with a novel bi-allelic mutation in IL12RB1 gene
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Serum vitamin D levels during activation and remission periods of patients with juvenile idiopathic arthritis and familial Mediterranean fever
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Late-diagnosed phenylketonuria in an eight-year-old boy with dyslexia and attention-deficit hyperactivity disorder
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Coexistence of early onset sarcoidosis and partial interferon-γ receptor 1 deficiency
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Recognizing immunodeficiency in children with recurrent infections: What are the predictive factors?
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Increasing vitamin D deficiency in children from 1995 to 2011
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Treatment of a patient with Kawasaki disease associated with selective IgA deficiency by continuous infusion of cyclosporine A without intravenous immunoglobulin
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Predictors of methotrexate response in Turkish children with oligoarticular and polyarticular juvenile idiopathic arthritis
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p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency
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Systems-level analysis of genome wide association study results for a pilot juvenile idiopathic arthritis family study
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Vitamin D receptor gene polymorphisms in children with kidney stone disease
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Subtype frequencies, demographic features, and remission rates in juvenile idiopathic arthritis – 265 cases from a Turkish center
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Is there clinical value in counting nucleated red blood cells and platelet indices in primary immunodeficiency disease?
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Investigation of the frequency of iron insufficiency among infants in a population in which routine iron supplementation is implemented
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Advantage of the subcutaneous immunoglobulin replacement therapy in primary immunodeficient patients with or without secondary protein loss
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Folate deficiency in patients with classical galactosemia: A novel finding that needs to be considered for dietary treatments
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Asymptomatic intracranial hemorrhage in a newborn with congenital factor VII deficiency and successful treatment with recombinant activated factor VII
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Coexistence of 2 rare autosomal recessively inherited disorders manifesting with immune deficiency; IL-12 receptor β1 and biotinidase deficiencies
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A novel mutation of interleukin-1 receptor antagonist (IL1RN) in a DIRA patient from Turkey: Diagnosis and treatment
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Sustained hyperferritinemia in a child with macrophage activation syndrome secondary to systemic juvenile idiopathic arthritis - perforinopathy: case based review
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A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism
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Severe iron deficiency anemia and anasarca edema due to excessive cow`s milk intake
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Clinical findings and genetic analysis of the patients with IL-12Rβ1 deficiency from southeast Turkey
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Atypical phenotype of an old disease or typical phenotype of a new disease: deficiency of adenosine deaminase 2
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Tocilizumab treatment in juvenile idiopathic arthritis patients: A single center experience
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The impact of 21-hydroxylase deficiency on cardiac repolarization changes in children with 21-hydroxylasedeficient congenital adrenal hyperplasia
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Alpha methyl acyl CoA racemase deficiency: Diagnosis with isolated elevated liver enzymes
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The case of pyridoxine dependent epilepsy misdiagnosed as non-ketotic hyperglycinemia
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The effect of 2000 ıu/day vitamin D supplementation on insulin resistance and cardiovascular risk parameters in vitamin D deficient obese adolescents
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Systemic onset juvenile idiopathic arthritis: a single center experience
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Thymic output changes in children with clinical findings signaling a probable primary immunodeficiency
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A novel mutation in SLC2A1 gene causing GLUT-1 deficiency syndrome in a young adult patient
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Detection of allele frequencies of common c. 511C>T and c.625G>A variants in the ACADS gene in the Turkish population
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A novel homozygous nonsense mutation (p.Y78*) in TMPRSS6 gene causing iron-refractory iron deficiency anemia (IRIDA) in two siblings
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Wernicke`s encephalopathy manifesting with diplopia after ileojejunostomy: report of a pediatric case with Hirschsprung disease
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Effect of gestational diabetes on the vitamin D levels in the neonates: a case control study
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Children with chronic-refractory autoimmune cytopenias: a single center experience
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A neglected cause of recurrent rhabdomyolysis, LPIN1 gene defect: a rare case from Turkey
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A novel compound heterozygous variant in CYP19A1 resulting in aromatase deficiency with normal ovarian tissue
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A rare cause of hepatomegaly and dyslipidemia: lysosomal acid lipase deficiency
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Atypical presentation in patients with 17 α-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature
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Evaluation of serum/salivary levels of carnosine and cotinine in recurrent wheezing of young children with passive smoking
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Whole exome sequencing identifies a novel variant in ABCA3 in an individual with fatal congenital surfactant protein deficiency
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Severe isolated sulfide oxidase deficiency with a novel mutation
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Effect of maternal and infant vitamin D supplementation on vitamin D levels of breastfed infants
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Cancer and constitutional Mismatch Repair Deficiency syndrome due to homozygous MSH 6 mutation in children with Café au Lait Spots and review of literature
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Hematopoietic stem cell transplantation complicated with EBV associated hemophagocytic lymphohistiocytosis in a patient with DOCK2 deficiency
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Mitochondrial trifunctional protein deficiency as a polyneuropathy etiology in childhood
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Iron deficiency is not always innocent in childhood: a rare diagnosis of collagenous gastritis
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Recommendations on phenylketonuria in Turkey
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Association between serum vitamin A, D and E status and respiratory distress syndrome in preterm infants – a propensity score matching analysis
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AA amyloidosis presenting with acute kidney injury, curable or not?
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Pyruvate kinase deficiency mimicking congenital dyserythropoietic anemia type I
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Evaluation of patients diagnosed with phenylketonuria and biotinidase deficiency by the newborn screening program: a ten-year retrospective study
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Significance of intestinal alkaline phosphatase in predicting histological activity of pediatric inflammatory bowel disease
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Cerebral developmental venous anomalies in children with mismatch repair deficiency
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Spontaneous hyphema in juvenile idiopathic arthritis uveitis
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