The Turkish Journal of Pediatrics
Smilar Issues: 55 Record Found
Visceral leishmaniasis and Coombs' positive hemolytic anemia: a rare association in an infant treated with liposomal amphotericin B
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Anemic or not?
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Successful management of severe chronic autoimmune hemolytic anemia with low dose cyclosporine and prednisone in an infant
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Management of renal anemia
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Neutrophil hypersegmentation and thrombocytosis in children with iron deficiency anemia
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A rare cause of anemia and thrombocytopenia in a newborn: congenital malaria
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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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Autoimmune hemolytic anemia as presenting manifestation of primary splenic anaplastic large cell lymphoma
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The validity of pallor as a clinical sign of anemia in cases with beta-thalassemia
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Community-acquired pneumonia and parapneumonic effusions in developing countries
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Plummer-Vinson Syndrome in a 15-Year-Old Boy
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Physiological periostitis in a 2.5-month-old baby
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Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness
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Neonatal gastrointestinal perforation
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A rare cause of mental motor retardation: recessive congenital methemoglobinemia type II
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Two new cases with Pearson syndrome and review of Hacettepe experience
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Seasonal and gender differences in hemoglobin value in infants at 5-7 months of age
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Maternal and Environmental Determinants of Breast-Milk Mercury Concentrations
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Fetal Malnutrition and Its Impacts On Neonatal Outcome In Preterm Infants
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Nasal Congenital Fibrolipomatous Hamartoma in a Premature Infant
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A Community-Based Iron Supplementation Program, “Iron-Like Turkey”, and the Following Prevalence of Anemia among Infants Aged 12-23 Months
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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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Iron deficiency anemia in late-preterm infants
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Scabies mimicking mastocytosis in two infants
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A Report of Adenocarcinoma In Situ and Congenital Pulmonary Airway Malformation in a Three-Day-Old Infant with a Review of the Literature
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Severe Iron Deficiency Anemia and Marked Eosinophilia in Adolescent Girls with the Diagnosis of Human Fascioliasis
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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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Bilateral Congenital Cataracts in an Infant with Klinefelter Syndrome
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A Newborn with Pertussis Accompanying Nephrotic Syndrome
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The Effect of Gynecomastia on Body Image Perception and Gender Roles in Adolescents
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The evaluation of acquired aplastic anemia in children and unexpected frequency of varicella-zoster virus association: a single-center study
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The Seasonal Variations of Respiratory Syncytial Virus Infections in Turkey: A 2-year Epidemiological Study
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Molecular Diagnosis of Fanconi Anemia with Next-Generation Sequencing in a Case with Subtle Signs and a Negative Chromosomal Breakage Test
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“Silent” β-thalassemia mutation (promoter nt-101 C > T) with increased hemoglobin A2
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Gender differences in defense mechanisms, ways of coping with stress and sense of identity in adolescent suicide attempts
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Ceftriaxone-induced hemolytic anemia in a child successfully managed with intravenous immunoglobulin
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Recessive congenital methemoglobinemia in immediate generations
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A case report of a 4-year-old child with glucose-6-phosphate dehydrogenase deficiency: An evidence based approach to nutritional management
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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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Restless leg syndrome in children with celiac disease
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Hereditary spherocytosis: Retrospective evaluation of 65 children
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Arrhythmia in thiamine responsive megaloblastic anemia syndrome
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Severe iron deficiency anemia and anasarca edema due to excessive cow`s milk intake
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Fanconi anemia: a single center experience of a large cohort
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Outcome of allogeneic Hematopoietic Stem Cell Transplantation on Diamond-Blackfan anemia using busulfan-based myeloablative regimen
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A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome
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A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome
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An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment
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Red blood cell variables and correlations with body mass components in boys aged 10-17 years
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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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Evaluation of retinal nerve fiber layer and choroidal thickness with spectral domain optical coherence tomography in children with sickle cell anemia
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A case of pediatric psoriasis achieving remission after allogenic bone marrow transplantation
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Pyruvate kinase deficiency mimicking congenital dyserythropoietic anemia type I
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Lactoferrin as treatment for iron-deficiency anemia in children: a systematic review
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