Turkish Journal of Pediatrics
- Investigating the risk factors for antibiotic lock therapy failure in pediatric cancer: a single center retrospective analysis
- Screening traumatic life events in preschool aged children: cultural adaptation of Child and Adolescent Trauma Screen (CATS) Caregiver-report 3-6 years version
- Mucormycosis in a pediatric population: a review of 20 cases from southern Turkey
- Comparison of four different non-invasive respiratory support techniques as primary respiratory support in preterm infants
- Characteristics and outcomes of critically ill children transported by ambulance in a Turkish prehospital system: a multicenter prospective cohort study
- Over restrictive elimination of foods in children with food allergy
- The HLA groups and their relationship with clinical features in Turkish children and adolescents with celiac disease
- Clinic and demographic characteristics of pediatric patients with Lichen sclerosus
- Nasopharyngeal carcinoma in a child with Kartagener’s syndrome
- A rare intrauterine onset growth retardation syndrome caused by mosaic 19p13.3 microduplication: evaluation of GH/IGF- 1 axis and GH therapy response
- Evaluation of injury-related under-five mortality in Turkey between 2014-2017
- Endonasal choanal atresia repair; evaluating the surgical results of 58 cases
- Complicated pneumonia due to exogenous toxic substances in children
- Brachial plexopathy as a consequence of nerve root swelling after shoulder trauma in a patient following an acute seizure
- Ophthalmologic approach to babies with cerebral visual impairment
- Shaken baby syndrome resulting in death: a case series
- Oral health status of asthmatic children using inhaled corticosteroids
- Acute hemorrhagic edema of infancy – is it really a mild, benign disease?
- The general movements assessment and effects of an early intervention in an infant with Cri du chat syndrome: a case report
- Headache, cataract, and unilateral visual loss: unusual features of DARS2 variants in LBSL
- Evaluation of micronutrient levels in children and adolescents with obesity and their correlation with the components of metabolic syndrome
- Practice, self-confidence and understanding of pediatric obstructive sleep apnea survey among pediatricians
- Fecal elastase levels in children diagnosed with functional abdominal pain-not otherwise specified
- Whole exome sequencing identifies a novel variant in ABCA3 in an individual with fatal congenital surfactant protein deficiency
- Massive true thymic hyperplasia in a 3-month-old infant: case report and literature review
- Facial colliculus syndrome due to a Herpes simplex virus infection following Herpes labialis
- Health insurance status and outcomes in children, adolescents, and young adults: a systematic review and meta-analysis
- IgE mediated food allergy in Turkey: different spectrum, similar outcome
- Enablers and barriers for enteral feeding with mother’s own milk in preterm very low birth weight infants in a tertiary care neonatal intensive care unit
- The performance of shear wave elastography on evaluating liver changes in obese and overweight children
- Outbreak of late-onset Group B Streptococcal disease with serotype Ib in a Neonatal Intensive Care Unit
- Timeliness of postnatal surgery in newborns with open neural tube defects: a single center experience
- Clinical and molecular characteristics of carnitineacylcarnitine translocase deficiency with c.270delC and a novel c.408C>A variant
- A very rare cause of protein losing enteropathy: Gaucher disease
- Severe isolated sulfide oxidase deficiency with a novel mutation
- Intranasal supernumerary tooth in a child: a case report
- Asthma and risk factors in the first 6 years of life in a population-based cohort
- Assessment of sleep in children with periodic fever, aphthous stomatitis, pharyngitis, and adenitis syndrome
- Developmental parameters and physical fitness in preschool children with Minor Neurological Dysfunction
- Developmental evaluation in children experiencing febrile convulsions
- The causes of parental vaccine refusal: results of a survey from Giresun, Turkey
- Treatment results of modified BFM protocol in pediatric high-risk Burkitt lymphoma
- Expression of MicroRNA 146a, 155, 181 and 223 in febrile seizure
- Clinical profile and long-term outcome of the first seizures in children
- Determining the effect of time dependent and time independent factors on pneumonia of children under five in North west Ethiopia
- Effects of lockdown during corona pandemic on children with neurodevelopmental disorders-A questionnaire-based survey
- Cost of illness of RSV infection in a middle-income tropical country
- Tobacco use among working adolescents and high school students in Turkey: evaluating the effect of the national tobacco control policy
- Autism spectrum disorder in patients with inherited metabolic disorders-a large sample from a tertiary center
- COVID-19-related anxiety in phenylketonuria patients
- Anxiety among the parents of pediatric patients receiving IVIG therapy during the Covid-19 pandemic
- Screen media exposure in pre-school children in Turkey: the relation with temperament and the role of parental attitudes
- Can peripheral blood monocyte percentage and lymphocyte monocyte ratio at diagnosis predict survival in pediatric neuroblastoma patients?
- Cancer and constitutional Mismatch Repair Deficiency syndrome due to homozygous MSH 6 mutation in children with Café au Lait Spots and review of literature
- Ketogenic diet therapy map of Turkey
- Neuropsychiatric lupus in Malaysian children: clinical characteristics, imaging features and 12-month outcomes
- Cardiac arrest due to a fatal dose of propranolol successfully treated with intravenous lipid infusion
- Diphallia: a case report of a rare anomaly evaluated by magnetic resonance imaging
- Ileal atresia and severe cerebral injury after fetoscopic laser photocoagulation treatment for twin-to-twin transfusion syndrome
- Entero-encephalopathy due to FBXL4-related mtDNA depletion syndrome
- Mesenteric tissue oxygenation status on the development of necrotizing enterocolitis
- Motor functions, quality of life and maternal anxiety and depression in children with cerebral palsy of different intelligence levels
- The possible association between neonatal morbidities and amniotic fluid pH and electrolyte levels in infants of preeclamptic mothers
- An unusual neurologic presentation of pediatric neuroinvasive West Nile virus infection: ophthalmoplegia
- Assessment of PD-L1 expression in patients with neuroblastoma and renal tumors
- Umbilical artery to common femoral artery (CFA) transposition, a novel technique for limb salvage in a newborn: a case report
- Comparison of serum anti-neuronal antibody levels in patients having autism spectrum disorder with and without regression
- Evaluation of red meat allergy patients and review of the literature
- The relationship of motor development with sensory processing among infants born very preterm: a prospective case-control study
- Evaluation of retinal nerve fiber layer and choroidal thickness with spectral domain optical coherence tomography in children with sickle cell anemia
- A fatal interstitial lung disease in an anti-melanoma differentiation-associated gene 5 (anti-MDA5) antibody negative patient with juvenile dermatomyositis
- Cockayne syndrome type: a very rare association with hemorrhagic stroke
- Tuberculosis risk in the biologic era: tuberculin skin test conversion rates in children with rheumatologic diseases
- Could plasma based therapies still be considered in selected cases with atypical hemolytic uremic syndrome?
- Predictive factors of high-flow nasal cannula oxygen therapy failure in children with respiratory distress treated in a Pediatric Emergency Department
- Investigation of immunity against Bordetella pertussis in pregnant women and an overview of the vaccination schedule in Turkey
- Cerebral sinovenous thrombosis in children: clinical presentation, locations, and acquired and inherited prothrombotic risk factors
- Turkish reference ranges for the left fetal modified myocardial performance index
- Parental knowledge about familial Mediterranean fever: a cross-sectional study
- The relationship between immature platelet fraction and severity of acute bronchiolitis
- A case of pediatric psoriasis achieving remission after allogenic bone marrow transplantation
- Allergic reactions during childhood vaccination and management
- Clinical characteristics, late effects and outcomes in pineoblastomas in children: a single center experience
- Cost and length of hospital stay for healthcare facility- onset Clostridioides Difficile infection in pediatric wards: a prospective cohort analysis
- The rare reason of pain in hip girdle: Mucolipidosis type 3 gamma
- Short and long term side effect of colistin treatment in preterm infants
- Thiol / disulfide balance and oxidative stress parameters in pediatric patients diagnosed with acute and chronic idiopathic thrombocytopenic purpura
- Evaluation of medication errors in pediatric patients using antibiotics
- Microbiological characteristics and outcomes of children with pleural empyema admitted to a tertiary hospital in southeast China, 2009-2018
- Clinical follow-up of children with high vitamin B12 values: should we worry?
- Hematopoietic stem cell transplantation complicated with EBV associated hemophagocytic lymphohistiocytosis in a patient with DOCK2 deficiency
- Primary spinal multifocal intradural-extramedullary Ewing sarcoma in children: presentation of a case and review of the literature
- Mitochondrial trifunctional protein deficiency as a polyneuropathy etiology in childhood
- Covid-19 in a patient with Familial Hemophagocytic Lymphohistiocytosis in children
- Case report: early onset narcolepsy initially misdiagnosed as obstructive sleep apnea syndrome
- Demographic, ocular and associated neurological findings in corpus callosum malformations
- Assesment of obesogenic factors in school-age children
- Aspirin-induced hepatotoxicity and anemia in children with acute rheumatic fever
- Altered gut microbiota is associated with feeding intolerance in preterm infants
- Burkholderia cepacia complex bacteremia outbreaks among non-cystic fibrosis patients in the pediatric unit of a university hospital
- An examination of the characteristics of mothers neglecting their children
- The relationship between particulate matter and childhood respiratory complaints and peak expiratory flows in Harran agricultural area
- How effective is family counselling on screen exposure of pre-school children?
- Evaluation of ultrasonographic optic nerve sheath diameter and central retinal artery Doppler indices by point-of-care ultrasound in pediatric patients with increased intracranial pressure
- Is there a relationship between joint hypermobility and gastrointestinal disorders in children?
- Brown Vialetto Van Laere syndrome: presenting with left ventricular non-compaction and mimicking mitochondrial disorders
- Unexpected condition in a rare disease: encephalopathy in early-onset sarcoidosis
- The role of plasma exchange in acute liver failure of autoimmune etiology
- Infantile systemic lupus erythematous presenting as nephrotic syndrome in a 12-month-old boy: a case report
- Upward trend in the frequency of community-acquired methicillin-resistant Staphylococcus aureus as a cause of pediatric skin and soft tissue infections over five years: a cross-sectional study
- The functional health status of children with cerebral palsy during the COVID-19 pandemic stay-at-home period: a parental perspective
- Thrombin generation in children with febrile neutropenia
- Transient positivity of anti-tissue transglutaminase IgA autoantibody in febrile children: a case-control study
- The assesment of prothrombotic potential using thrombin generation assay in pediatric patients with nephrotic syndrome: preliminary study
- Rare presentation of levamisole-induced leukoencephalopathy in a pediatric patient: seizure
- Mild encephalopathy with reversible extensive white matter lesions in a child with acute adenoviral infection and a literature review
- A case report of intracranial hypertension and aseptic meningitis: anti-tumor necrosis factor associated or juvenile idiopathic arthritis related
- Vogt Koyanagi Harada syndrome in a 15-year-old girl, steroids side effects and recurrences
- Interaction of functional gastrointestinal disorders with postpartum conditions related to mother and baby
- Neonatal diabetes mellitus due to a new KCNJ11 mutation - 10 years of the patient’s follow-up
- Healthcare workers’ knowledge level regarding anaphylaxis and usage of epinephrine auto-injectors
- Seroprevalence of Anti- N-methyl-D-aspartate receptor antibodies in children with seizures of unknown cause
- Evaluation of serum/salivary levels of carnosine and cotinine in recurrent wheezing of young children with passive smoking
- Clinical and demographic characteristics of childhood neuro-ophthalmology diseases at a tertiary eye care center
- Oral health status in children with familial Mediterranean fever
- Early-auditory intervention in children with hearing loss and neurodevelopmental outcomes: cognitive, motor and language development
- A rare case of juvenile amyotrophic lateral sclerosis
- Sertoli-Leydig cell tumor, thyroid follicular carcinoma and rhabdomyosarcoma of the uterine cervix in a prepubertal girl with pathogenic germline variant in DICER1 gene
- Anaphylaxis to levetiracetam in an adolescent: a very rare occurence
- The role of culture on parenting boys as a potential risk factor in the development of male eating disorders during adolescence in Turkey
- Infantile tremor syndrome secondary to peroral vitamin B12 replacement therapy: a report of two cases with myoclonus
- The comparison and diagnostic accuracy of different types of thermometers
- Pediatric hospital healthcare workers and pertussis; a seroprevalence study
- Relationship between tumor viability during treatment and the clinical outcomes of patients with bladder/prostate rhabdomyosarcoma: a single-center experience
- Tracking postural stability of children and adolescents after a concussion: sport-related versus non-sport-related concussion
- Can early hyperglycemia affect the morbidity/mortality of very low birth weight premature infants?
- Children with cervical lymphadenopathy: reactive or not?
- Enthesitis: an obscured extraintestinal manifestation in pediatric inflammatory bowel disease
- Using lactate dehydrogenase to predict the severity of respiratory distress in term newborn infants with no perinatal asphyxia
- Investigation of the relationship between cord clamping time and risk of hyperbilirubinemia
- Neonatal outcomes of early- and late-onset preeclampsia
- Duration of treatment with oral rehydration salts for vasovagal syncope in children and adolescents
- A novel compound heterozygous variant in CYP19A1resulting in aromatase deficiency with normal ovarian tissue
- High-grade neuroepithelial tumor with medulloepithelioma-like areas out of the central nervous system in an infant with hemihypertrophy: a unique association
- Atypical presentation in patients with 17 α-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature
- Successful treatment of pediatric post-liver transplant Kaposi’s sarcoma with paclitaxel
- Ascites: a loadstar for the diagnosis and management of an intracranial tumor
- Nosocomial pneumonia caused by water-born Legionella pneumophila in a pediatric hematopoietic stem cell transplantation recipient for thalassemia major
- Abusive head trauma: two cases and mini-review of the current literature
- Rituximab-induced serum sickness and anaphylaxis in a child with nephrotic syndrome
- A rare cause of hepatomegaly and dyslipidemia: lysosomal acid lipase deficiency
- Temporal bone hemangioendothelioma as a rare vascular tumor in childhood: case report and review of the literature
- Are homozygous SLC19A3 deletions non-responsive to thiamine/biotin?
- Response to “Neonatal form of biotin-thiamine-responsive basal ganglia disease. Clues to diagnosis”
- SCN1A mutation spectrum in a cohort of Bulgarian patients with GEFS+ phenotype
- The incidence and clinical effects of Bordetella pertussis in children hospitalized with acute bronchiolitis
- The experiences, perceptions and challenges of mothers managing asthma in their children: a qualitative study
- Clinical characteristics of children with congenital anomalies of the kidney and urinary tract and predictive factors of chronic kidney disease
- Turkish validation of the maternal responsiveness global rating scale in slow-to-talk toddlers
- A rare cause of inguinal abscess: perforated appendicitis due to foreign body in Amyand’s hernia
- Takayasu arteritis presenting with spontaneous pneumothorax
- Point-of-care ultrasound use in pediatric intensive care units in Turkey
- Carbapenem and colistin resistance in children with Enterobacteriaceae infections
- A national survey on use of less invasive surfactant administration in Turkey
- Gender-related differences in etiology of organic central precocious puberty
- Local allergic rhinitis: a pediatric perspective
- Assesment of colistin related side effects in premature neonates
- Predictive value of an early amplitude-integrated electroencephalogram for short-term neurologic outcomes in preterm infants
- Immediate adverse reactions to intravenous immunoglobulin in primary immune deficiencies: a single center experience
- Is there any relationship between initial hematological parameters and severity of scorpion envenomation?
- Role of kallistatin in pediatric patients with pulmonary arterial hypertension
- Evaluating the effects of different doses of ursodeoxycholic acid on neonatal jaundice
- Emotional support for parents with premature children admitted to a neonatal intensive care unit: a qualitative phenomenological study
- Management of pediatric cardiac transplantation candidates with pulmonary hypertension and high pulmonary vascular resistance
- Corneal endothelial morphology and anterior segment parameters in children with type 1 diabetes mellitus
- Two cases of Vici syndrome presenting with corpus callosum agenesis, albinism, and severe developmental delay
- Pyloroduodenal intussusception due to diffuse juvenile polyposis in a 3 year-old child: case report
- Zinc deficiency and febrile seizure: a systematic review and meta-analysis
- Effect of long-term glucocorticoid therapy on bone mineral density of the patients with congenital adrenal hyperplasia
- New guidelines for diagnosis of rheumatic fever; do they apply to all populations?
- Congenital myotonia: a review of twenty cases and a new splice-site mutation in the CLCN1 gene
- The remarkable response to ponatinib therapy in a child with blastic phase of chronic myeloid leukemia
- Recurrent debilitating calf pain associated with fasciitis in Familial Mediterranean fever and response to canacinumab
- A mysterious case with abdominal pain and syndrome of inappropriate anti-diuretic hormone secretion
- Variant ataxia-telangiectasia in a child presenting with laryngeal dystonia
- A new location for pediatric immunoglobulin G4 related disease: the biceps muscle
- Low function of natural killer cells in treated classic Menkes disease
- Eczema herpeticum emerging during atopic dermatitis in infancy
- Retrospective evaluation of childhood paraphenylenediamine intoxication due to black henna
- Effect of gestational diabetes on the vitamin D levels in the neonates: a case control study
- Choroid plexus papilloma in extragonadal teratoma with predominantly neurogenic elements: a case report and review of the literature
- Congenital esophageal diverticulum in a very low birth weight infant: case report and review of literature
- Iatrogenic nasal synechiae in a premature newborn
- Neurocognitive abilities in individuals with Down syndrome-a narrative review
- Successful intraosseous adenosine administration in a newborn infant with supraventricular tachycardia
- Peritoneal dialysis as a life-saving procedure in an extremely low birth weight infant: case report and review of the literature
- Healthy eating index in a nationally representative sample of children and adolescents by socio-demographic characteristics: the Weight disorders survey of the CASPIAN-IV Study
- Fecal calprotectin levels in Helicobacter pylori gastritis in children
- Emotion regulation in adolescents with acne vulgaris: correlates of medication adherence, clinical dimensions and psychopathology symptoms: a cross-sectional study
- Serum levels of VEGF and bFGF in infantile hemangiomas treated with propranolol
- Clinical evaluation of the effectiveness of interferential current therapy in the treatment of children with pelvic floor dyssynergia-type constipation: a randomized controlled study
- Evaluation of blood pressure responses to treadmill exercise test in normotensive children of hypertensive parents
- Is being small for gestational age a risk factor for strabismus and refractive errors at 3 years of age?
- A case of fulminant pneumococcus meningoencephalitis progressing with white matter involvement despite two doses of conjugated pneumococcus vaccine
- Uncoupling protein gene UCP1-3826A/G, UCP2 Ins/Del and UCP3-55C/T polymorphisms in obese Turkish children
- The effect of warts on quality of life in Turkish pediatric patients
- Internal carotid artery dissection following blunt head trauma: a pediatric case report and review of the literature
- Clitoromegaly caused by ovarian stimulation in a preterm newborn: ovarian hyperstimulation syndrome of preterm babies
- A rare pediatric case of neurobrucellosis with bilateral optic neuritis
- Pediatric Bell’s palsy: prognostic factors and treatmentoutcomes
- Off-label drug use in pediatric patients: a comparative analysis with nationwide routine prescription data
- Nationwide efforts for trauma-informed care implementation and workforce development in healthcare and related fields: a systematic review
- Life-stage factors associated with overweight severity inadolescents
- Comparative study of various therapeutic modalities for Guillain Barré syndrome in Assiut University Children Hospital
- Sensory profile, ferritin and zinc levels in preschool-aged children with symptoms of attention deficit hyperactivity disorder
- Determinants of outcomes in chronic pediatric peritoneal dialysis: a single center experience
- Risk factors of intravenous immunoglobulin resistance and coronary arterial lesions in Turkish children with Kawasaki disease
- Cord blood delta neutrophil index values of term neonates
- Infection risk after paediatric liver transplantation
- Assessment of motor development using the Alberta Infant Motor Scale in full-term infants
- A novel homozygous nonsense mutation (p.Y78*) in TMPRSS6 gene causing iron-refractory iron deficiency anemia (IRIDA) in two siblings
- Early-onset neonatal sepsis caused by Neisseria meningitidisserogroup B: case report and literature review of a 102-year period
- Dropped head related lamin A/C associated congenital muscular dystrophy case; previously defined as emery-dreifuss muscular dystrophy
- Obstructive jaundice and severe pancreatitis due to the foramen of Winslow hernia with multiple anomalies
- A rare cause of acute abdominal pain in a patient with Primary ciliary dyskinesia with situs inversus totalis
- Gross motor development of preschool children: effects of socioeconomic status and maternal education
- Detection of allele frequencies of common c. 511C>T and c.625G>A variants in the ACADS gene in the Turkish population
- Clinical and laboratory predictors of survival for pediatric patients on non-postcardiotomy extracorporeal membrane oxygenation (ECMO)
- Evaluation of pentraxin 3 level and cardiac functions in psoriatic children
- Mother-child interaction and the development status of children who have been accidentally poisoned
- Factors affecting the success of pediatric extracorporeal shock wave lithotripsy therapy: 26-year experience at a single institution
- Grisel’s syndrome presenting with neck pain: an atypical case
- A rare presentation of adrenal adenoma in infancy: isolated Cushing’s syndrome
- Children with extreme hyperferritinemia are at risk of receiving more chemotherapy than necessary
- Red blood cell variables and correlations with body mass components in boys aged 10-17 years
- Cardiorespiratory parameters in newborns during sedation with chloral hydrate
- Are general movements at 3-5 months correlated and compatible with the Bayley-III at 1,5-2 years age?
- A rare cause of epileptic encephalopathy: a beta-propeller protein associated neurodegeneration case with a new mutation and literature review
- Novel mutation and severe respiratory failure in congenital disorders of glycosylation Type Ix
- Rotavirus encephalopathy with concomitant acute cerebellitis: report of a case and review of the literature
- Peters Plus syndrome: a recognizable clinical entity
- Neonatal iliopsoas abscess presenting with transient cyanosis of a single extremity: a case report and review of the literature
- Diverse clinical characteristics of Aspergillus growth in patients with cystic fibrosis
- Clinical features and treatment of ruptured pulmonary hydatid cyst in children
- Muscle strength and joint health in children with hemophilia: a cross-sectional study
- A rare cause of secondary hemophagocytic lymphohistiocytosis: systemic loxoscelism
- Two patients with glutaric aciduria type 3: a novel mutation and brain magnetic resonance imaging findings
- Extracorporeal shock wave lithotripsy in the management of a 14-year-old girl with chronic calcific pancreatitis
- Type 4 hypersensitivity development in a case due to mifamurtide
- Giant ethmoidal mucocele leading to proptosis and hypertelorism in a pediatric patient with cystic fibrosis: a case report
- Two-year old girl with glial choristoma presented in a thyroglossal duct cyst
- Pacemaker lead-induced tricuspid stenosis treated with percutaneous valvotomy
- Xanthogranulomatous pyelonephritis due to calculi in a 5-year-old girl
- Terlipressin in the treatment of neonatal refractory hypotension caused by septic shock: a case report
- Bleeding characteristics and management of minor surgeries in rare bleeding disorders: report from a Turkish Pediatric Hematology Center
- Coronary artery fistulae and treatment in children
- Bee product efficacy in children with upper respiratory tract infections
- Children with chronic-refractory autoimmune cytopenias: a single center experience
- Orbital complications of pediatric rhinosinusitis: A single institution report
- Circulating Epstein-Barr virus DNA and cell-free DNA in pediatric lymphomas
- Awareness assessment for parents of children with congenital heart diseases regarding fetal echocardiography
- Intratracheal administration of budesonide with surfactant in very low birth weight infants to prevent bronchopulmonary dysplasia
- A partial response to abatacept in a patient with steroid resistant focal segmental glomerulosclerosis
- A neglected cause of recurrent rhabdomyolysis, LPIN1 gene defect: a rare case from Turkey
- Different clinical presentation in a patient with two novel pathogenic variants of the FBXL4 gene
- Neuropsychological outcome in cases with acute disseminated encephalomyelitis
- Pigeon breeder’s disease as a cause of hypersensitivity pneumonia in children
- Maternal and fetal tuberous sclerosis complex: a case report questioning clinical approach
- Kawasaki disease presented with status epilepticus and diffusion MRI abnormalities in the subcortical white matter
- Clinical manifestation and outcomes of children with hypertrophic cardiomyopathy in Kosovo
- Bone marrow involvement in pediatric malignancies: a comparison study of Positron emission tomographycomputed tomography and bone marrow biopsy
- Tetanus; a forgotten infection disease: a report of two cases
- Clinically isolated syndrome and multiple sclerosis in children: a single center study
- A rare case of syndromic severe congenital neutropenia: JAGN1 mutation
- Increased potassium excretion in children with monosymptomatic nocturnal enuresis: could it be related to Kir 4.1- KCNJ10 gene polymorphism?
- Outcomes and prognostic factors for pediatric cancer patients admitted to an intensive care unit in a university hospital
- Ambulatory arterial stiffness index is increased in obese children
- Congenital afibrinogenemia in a 4-year-old girl complicated with acute lymphoblastic leukemia
- Mild encephalopathy with reversible splenial lesion associated with echovirus 6 infection: a case report and review of the literature
- Acute necrotizing encephalopathy with organic psychosis: a pediatric case report
- Does magnetic resonance imaging increase core body temperature in children? Results of the administration of propofol and ketofol: a randomized clinical study
- Aortic balloon valvuloplasty and mid-term results in newborns: a single center experience
- Performance of SNAPPE-II score in neonatal sepsis: an experience from a tertiary care center
- Wernicke’s encephalopathy manifesting with diplopia after ileojejunostomy: report of a pediatric case with Hirschsprung disease
- Pediatric case of persistent hiccups associated with hypertrophic olivary degeneration
- Osteoarticular involvement of brucellosis in pediatric patients: clinical and laboratory characteristics
- Sacroiliitis associated with familial Mediterranean fever in childhood: a case series and review of literature
- Persistence of right umbilical vein: a singular case
- Children with lymphoma presenting with hemophagocytic lymphohistiocytosis
- The corrected QT interval prolongation in adolescents with cardiac iron overload β-thalassemia major
- Clinical and laboratory awareness for an under recognized pathogen in newborn meningitis: Mycoplasma Hominis: a case report
- Canakinumab in colchicine resistant familialMediterranean fever and other pediatric rheumatic diseases
- Treatment of maple syrup urine disease with high flow hemodialysis in a neonate
- Multimodality imaging findings of visceral myopathy in a child presenting with palpable abdominal mass
- Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis
- Clearance of jaundice after the modified Kasai’s operation predicts survival outcomes in patients with biliary atresia
- Nasal nitric oxide levels in primary ciliary dyskinesia, cystic fibrosis and healthy children
- Is serum procalcitonin level a reliable indicator in early diagnosis of congenital pneumonia?
- Body mass index is decreased in children and adolescents with postural tachycardia syndrome
- Does stable sitting influence upper limb function in children with cerebral palsy?
- A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism
- Effects of the storage of breast milk at different temperatures on total antioxidant capacity, total oxidant status, and paraoxonase-1 level
- Retinopathy of prematurity risk factors: Does human milk prevent retinopathy of prematurity?
- The effectiveness of serum amyloid A for prediction of neonatal cholestasis associated with parenteral nutrition in premature infants
- The pathogens and curative effects analysis of perianal abscess of infants under 3 months
- Bilateral Wilms tumors: Treatment results from a single center
- Is there any relation between connective tissue growth factor and scar tissue in vesicoureteral reflux?
- Prolonged QT dispersion is associated with pediatric syncope
- Acute lymphoblastic leukemia presenting as nephromegaly in a child: A rare case report
- Intrathecal baclofen use in the management of tetanus related spasm: A case report
- Successful radiofrequency ablation of accessory pathway associated with left atrial appendage aneurysm in a low birthweight premature patient
- Response to “Effect of iron supplementation during infancy period”
- Pulmonary complications following hematopoietic stem cell transplantation in children
- Severe iron deficiency anemia and anasarca edema due to excessive cow’s milk intake
- BK virus associated nephropathy and severe pneumonia in a kidney transplanted adolescent with Schimke immuneosseous-dysplasia
- Asymptomatic giant congenital left atrial aneurysm
- A rare clinical association: Barth syndrome and cystic fibrosis
- More than Ophelia syndrome: Multiple paraneoplastic syndromes in pediatric Hodgkin lymphoma
- Effect of iron supplementation during infancy period
- Invasive fungal infection in children with hematologic malignancy
- Tocilizumab treatment in juvenile idiopathic arthritis patients: A single center experience
- Renal features of Bardet Biedl syndrome: A single center experience
- Detection and molecular characterization of uncommon rotavirus group A genotype G12 among hospitalized children in Chennai
- Evaluation of growth in children and adolescents after renal transplantation
- A novel de novo KCNQ2 mutation in a child with treatmentresistant early-onset epileptic encephalopathy
- Alpha methyl acyl CoA racemase deficiency: Diagnosis with isolated elevated liver enzymes
- Fetal intrapericardial teratomas
- Comparison of i-gel, LMA-supreme, LMA-classic and LMAproseal as conduits of endotracheal intubation in newborns and infants: A manikin study
- The relationship between prenatal testosterone and developmental stuttering in boys
- Cigarette smoking in adolescents with type 1 diabetes mellitus and congenital adrenal hyperplasia
- The impact of 21-hydroxylase deficiency on cardiac repolarization changes in children with 21-hydroxylasedeficient congenital adrenal hyperplasia
- Clinical signs and symptoms of toxic serum digoxin levels in neonates
- A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome
- Neonatal form of biotin-thiamine-responsive basal ganglia disease. Clues to diagnosis
- Bismuth intoxication resulting in acute kidney injury in a pregnant adolescent girl
- Clinical, electrophysiological findings and evaluation of prognosis of patients with Guillain-Barré syndrome
- Comparison of diastolic function in children with transfusion dependent beta thalassemia major by tissue and conventional doppler imaging indices and its correlation with serum ferritin levels
- First report of human ehrlichiosis in Turkey
- A rare chromosomal disorder in a newborn: Trisomy 3q
- Giant axonal neuropathy: A differential diagnosis of consideration
- An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment
- Self-introduced intravesical magnets in a 3-year-old boy: Case report
- Hemophagocytic lymphohistiocytosis associated with oxcarbazepine
- Kawasaki disease complicated by peripheral gangrene and a ventricular septal defect: An unusual association
- Noninvasive respiratory support via nasal cannula in premature infants: Is it really safe?
- Etiology of vaginal discharge in sexually inactive adolescents
- Priapism: A rare presentation of precursor B-Cell acute lymphoblastic leukemia
- Clinical findings and genetic analysis of the patients with IL-12Rβ1 deficiency from southeast Turkey
- Outcome of allogeneic Hematopoietic Stem Cell Transplantation on Diamond-Blackfan anemia using busulfan-based myeloablative regimen
- IPEX syndrome: an easily-missed diagnosis of a life threatening condition
- Coexistence or a related condition: an infant with retinoblastoma and Gaucher disease
- A synchronous occurrence of bifocal intracranial germinoma and bilateral testicular epidermoid cyst in an adolescent patient with Klinefelter’s syndrome
- Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations
- Comparison of neonatal reference intervals for 23 biochemical analytes in the cord blood-A single center study in South Korea
- The relationships between nomophobia, alexithymia and metacognitive problems in an adolescent population
- Nitrogen balance of very preterm infants with extrauterine growth restriction
- The predictive value of procalcitonin, C-reactive protein, presepsin, and soluble-triggering receptor expressed on myeloid cell levels in bloodstream infections in pediatric patients with febrile neutropenia
- Clinical features and laboratory findings in children hospitalized with acute Epstein-Barr virus infection: a crosssectional study in a tertiary care hospital
- Comparison between the motor function of school-aged children with normal birth weight and children with low birth weight: a cross-sectional study
- The effects of enteral artificial amniotic fluid-containing erythropoietin on short term outcomes of preterm infants
- Correlation of the Bayley scales of infant-toddler development-3rd edition and neuro-sensory motor assessment in preterm infants during the first year of life.
- Thrombotic thrombocytopenic purpura as a rare cause of anemia with thrombocytopenia in childhood: report of 2 cases
- Infant lymphoblastic leukemia: a single centers 10 year experience
- Charcot-Marie-Tooth 1A concurrent with anaplastic ependymoma in a toddler: when an acute event unmasks a chronic condition
- A rare cause of vomiting in an adolescent: gastric Burkitt’s lymphoma
- Excision of the atrial Wilms’ tumor thrombus without sternotomy, atriotomy and cardiovascular By-pass
- Concomitance of Familial Mediterranean Fever and Gitelman syndrome in an adolescent
- Perforation of Meckel’s diverticulum in a very low birth weight neonate with severe pneumoperitoneum and review of literature
- A novel evaluation of genetic polymorphism in BCG adenitis
- Acute ischemic stroke following water immersion seizure: a case report
- Thirty years of the newborn screening program in Central Serbia: the missed cases of congenital hypothyroidism
- Chronic recurrent multifocal osteomyelitis in children: a single center experience over five years
- Atypical phenotype of an old disease or typical phenotype of a new disease: deficiency of adenosine deaminase 2
- Exercise-induced anaphylaxis: a case report and review of the literature
- Fanconi anemia: a single center experience of a large cohort
- Expression of the Toll-like receptors 2 gene as a genetic determinant of the formation of newborns multiple organ failure syndrome
- Two years of newborn screening for cystic fibrosis in Turkey: Çukurova experience
- Telomere length comparison between oral cells and blood cells among neonates
- Eleven-year surveillance of acute flaccid paralysis in southwestern Iran
- Impulse oscillometry reference values and correlation with predictors in Turkish preschool children
- Factors affecting mortality in children with dilated cardiomyopathy
- The potential utility of real-time PCR of the 16S-rRNA gene in the diagnosis of neonatal sepsis
- The contribution of morphine sulfate to the development of necrotizing enterocolitis in preterm infants: a matched casecontrol study
- Stevens-Johnson syndrome and toxic epidermal necrolysis: a report of six cases
- Reversible cardiomyopathy-tachycardiomyopathy in children
- Relationships between screen time, internet addiction and other lifestyle behaviors with obesity among secondary school students in the Turkish Republic of Northern Cyprus
- An adolescent case of extensive Behçet’s disease successfully treated with Infliximab
- The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome
- A novel LEMD3 pathogenic variant in a son and mother with osteopoikilosis
- Could you say that was an atrial flutter or not?
- Alpha gal specific IgE positivity due to tick bites and red meat allergy: the first case report in Turkey
- Medicolegal evaluation of a maternal filicide attempt: a case report
- Optic neuropathies in childhood: a review of etiology and treatment
- Cranial MR characteristics of Cerebral Palsy cases and correlation of findings with clinical results
- Unusual and early onset IPEX syndrome: a case report
- The case of pyridoxine dependent epilepsy misdiagnosed as non-ketotic hyperglycinemia
- Netherton syndrome previously misdiagnosed as hyper IgE syndrome caused by a probable mutation in SPINK5 C
- What triggered massive hemoptysis in Goodpasture syndrome with isolated pulmonary involvement in a 14-year-old boy?
- Complete atrioventricular block associated with clozapine intoxication: case report
- Systemic hypertension followed by insidious stroke in a 12-year-old boy with childhood neurofibromatosis type 1 presenting with renal and cerebral artery vasculopathy
- Benign migratory glossitis
- Maternal adipose tissue, antenatal steroids, and Respiratory Distress syndrome: complex relations
- Thymic output changes in children with clinical findings signaling a probable primary immunodeficiency
- Is antibiotic lock therapy effective for the implantable longterm catheter-related bloodstream infections in children?
- Childhood sclerosing cholangitis associations in a Tunisian tertiary care hospital: a many-faceted disease
- Bi-allelic mutations in PRUNE lead to neurodegeneration with spinal motor neuron involvement and hyperCKaemia
- A case of craniopagus parasiticus: an antenatal diagnosis by ultrasound screening at 16 weeks of gestation and a literature review of recently reported cases
- A novel mutation in SLC2A1 gene causing GLUT-1 deficiency syndrome in a young adult patient
- Pathological findings of central nervous system, two GM1 gangliosidosis autopsy cases
- A pediatric case of Ortner’s syndrome caused by heritable pulmonary arterial hypertension and review of the literature
- Response to: Arthropathy-like findings and a carpal tunnel syndrome as the presenting features of Scheie syndrome: Three cases from the same family
- The lung microbiome in neonates
- A comparison of bone mineral density in adolescent swimmers, pentathletes and figure skaters
- Long term follow-up of children with chronic hepatitis B: a single center experience
- Congenital heart disease and thyroid dysfunction in Down syndrome reported at Children’s Hospital, Lahore, Pakistan
- Rapid onset of altered mental status with progressive autonomic instability and hypoventilation in a 2-year-old male
- Schwartz Jampel syndrome responding positively to carbamazepine therapy: a case report and a novel mutation
- A neonate with tracheobronchial cobblestone mucosa presenting with acute severe hypercapnia
- Spontaneously resolved uterine prolapse in a neonate with spina bifida
- Pediatric primary anaplastic ganglioglioma with malignant neuronal component
- Systolic dysfunction of systemic ventricle in patients who underwent a Fontan operation
- Systemic onset juvenile idiopathic arthritis: a single center experience
- Fibrodysplasia ossificans progressiva – can we diagnose it right at the outset?
- Mental health of Syrian refugee adolescents: how far have we come?
- The role of cardiac troponin T in detection of cardiac damage and long term mortality in children with chronic renal disease
- Vedolizumab treatment in a patient with X-linked agammaglobulinemia, is it safe and efficient?
- Extracorporeal membrane oxygenation for the support of pediatric patients with acute fulminant myocarditis
- Multifocal mesenchymal hamartoma of the chest wall in a newborn
- Clinical experiences in Turkish paediatric patients with chronic recurrent multifocal osteomyelitis
- Heart rate variability in juvenile systemic lupus erythematosus patients
- Reliability and validity of the pediatric feeding and swallowing disorders family impact scale for Turkish children with cerebral palsy by endoscopic evaluation
- Acute ophthalmoparesis and persistent mydriasis: expanding the clinical spectrum of anti-GQ1b positive cranial neuropathy in a 5.5-year-old girl
- Pediatric mesenteric panniculitis: three cases and a review of the literature
- The possible concomitant use of aeroallergen and food panels for skin prick testing might enhance the risk of generalized allergic reactions in children
- Letter to the editor: Speech problems and speech delay: possible underdiagnosis of selective mutism
- Early onset inflammatory bowel disease: manifestations, genetics and diagnosis
- Serum Bcl-2, caspase-9 and soluble FasL levels as perinatal markers in late preterm pregnancies with intrauterine growth restriction
- Characteristics, diagnosis, and treatment modality of pediatric patients with cystic echinococcosis: a single centre experience
- Cardiometabolic risk factors in Turkish children with hepatosteatosis
- The factors related to mother's beliefs and behaviors concerning the prevention of poisoning among children under the age of five, using the Health Belief Model
- Complete and sustained resolution of calcinosis universalis in a juvenile dermatomyositis case with mycophenolate mofetil
- Familial reciprocal non robertsonian translocation t(14;22) resulting in 22q11.2 deletion syndrome
- Assessment of pediatric cricopharyngeal achalasia with high resolution manometry
- Impact of the mandatory Hepatitis A immunization program: before and after the vaccine in Ankara, Central of Turkey
- Long-term follow-up results of patients with ADCK4 mutations who have been diagnosed in the asymptomatic period: effects of early initiation of CoQ10 supplementation
- Hematological disturbances in Down syndrome: single centre experience of thirteen years and review of the literature
- A targeted salvage therapy with Brentuximab vedotin in heavily treated refractory or relapsed pediatric Hodgkin lymphoma patients before and after stem cell transplantation
- From Uganda to Italy: a case of nephrotic syndrome secondary to Plasmodium infection, Quartan malarial nephropathy and kidney failure
- Syncope due to acute rheumatic fever with pacemaker-like syndrome
- Elemental mercury intoxication in 7 patients admitted to a pediatric rheumatology clinic
- An infant with intradural extramedullary synovial sarcoma: the youngest case in the literature
- The effect of 2000 ıu/day vitamin D supplementation on insulin resistance and cardiovascular risk parameters in vitamin D deficient obese adolescents
- Response to “Speech problems and speech delay: possible underdiagnosis of selective mutism”
- Ewing sarcoma in an infant and review of the literature
- Congenital long-QT syndrome in type 1 diabetes: a unique association
- Ataxia, tremor, intellectual disability: a case of STXBP1 encephalopathy with a new mutation
- The factors related to mother's beliefs and behaviors concerning the prevention of poisoning among children under the age of five, using the Health Belief Model
- Impacts of phototherapy on DNA damage and total oxidant/ antioxidant status in jaundiced newborns
- Kawasaki disease in Turkish children: a single center experience with emphasis on intravenous immunoglobulin resistance and giant coronary aneurysms
- GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria
- Efficacy of rufinamide in childhood refractory epilepsy
- Hereditary spherocytosis: Retrospective evaluation of 65 children
- Birth outcomes after inadvertent use of category X drugs contraindicated in pregnancy: Where is the real risk?
- A case of atypically located leiomyoma mimicking axillary lymphadenomegaly
- A case of myeloid sarcoma presenting with an orbital mass, hearing loss, and multiple cranial neuropathies
- Polyarteritis nodosa in case of familial Mediterranean fever
- An infant case of renovascular hypertension in moyamoya disease treated by angioplasty
- The influence of media on the sleep quality in adolescents
- Granulomatous amebic encephalitis caused by Acanthamoeba in an immuncompetent child
- Chelation therapy for secondary neonatal iron over load: Lessons learned from rhesus hemolytic disease
- Arthropathy-like findings and a carpal tunnel syndrome as the presenting features of Scheie syndrome: Three cases from the same family
- Arrhythmia in thiamine responsive megaloblastic anemia syndrome
- Advantage of the subcutaneous immunoglobulin replacement therapy in primary immunodeficient patients with or without secondary protein loss
- High alert medications administration errors in neonatal intensive care unit: A pediatric tertiary hospital experience
- Gelsolin levels in patients with bronchiolitis
- Attitudes of physicians concerning vaccines not included in the national immunization schedule
- Neonatal atrial flutter: Three cases and review of the literature
- A case of steroid-resistance Hashimoto's encephalopathy presenting with sensorimotor polyneuropathy
- A novel mutation of the MYH7 gene in a patient with hypertrophic cardiomyopathy
- A case of steroid-resistance Hashimoto's encephalopathy presenting with sensorimotor polyneuropathy
- Glycemic control and health behaviors in adolescents with type 1 diabetes
- Perioperative factors associated with hyperglycemia after pediatric cardiac surgery and impact of hyperglycemia on morbidity and mortality
- Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome
- Investigation of antiviral resistance and escape mutations in children with naive chronic hepatitis B patients and their parents
- Does microbial resistance profile change in community-based intra-abdominal infections? Evaluation of the culture results of patients with appendicitis
- Plasma lipoxin A4 levels in childhood chronic spontaneous urticaria
- Frequency and findings of the acquired anorectal disease in the pediatric population with chronic constipation
- Asymptomatic intracranial hemorrhage in a newborn with congenital factor VII deficiency and successful treatment with recombinant activated factor VII
- A girl with Henoch Schönlein purpura associated with acute rheumatic fever and review of literature
- Coexistence of 2 rare autosomal recessively inherited disorders manifesting with immune deficiency; IL-12 receptor β1 and biotinidase deficiencies
- A novel mutation of interleukin-1 receptor antagonist (IL1RN) in a DIRA patient from Turkey: Diagnosis and treatment
- Ultrasound guided percutaneous central venous catheters in neonatal intensive care unit
- Outcome of out-of-hospital cardiopulmonary arrest in children: A multicenter cohort study
- Fever-induced Brugada syndrome in a 9-year-old boy presenting with acute chest pain
- Glycogen storage disease type 0 due to a novel frameshift mutation in glycogen synthase 2 (GYS2) gene in a child presenting with fasting hypoglycemia and postprandial hyperglycemia
- Sustained hyperferritinemia in a child with macrophage activation syndrome secondary to systemic juvenile idiopathic arthritis - perforinopathy: case based review
- Meconium periorchitis: An incidentally diagnosed rare entity during inguinal herniorraphy
- Pulmonary thromboendarterectomy in pediatric patients: Report of three cases
- Effects of Lactobacillus rhamnosus GG as a probiotic on neonatal hyperbilirubinemia
- Evaluation of psychological characteristics of Turkish children with type 1 diabetes mellitus from two demographically and geographically distinct regions
- Father’s role in infantile anorexia
- An extreme entity in differential diagnosis of musculoskeletal involvement-fibrodysplasia ossificans progressiva: a case based review
- Exhaled breath condensate magnesium levels of infants with bronchiolitis
- Treatment of severe leptospirosis with therapeutic plasma exchange in a pediatric patient
- Non-immune hydrops fetalis: A retrospective analysis of 151 autopsies performed at a single center
- Folate deficiency in patients with classical galactosemia: A novel finding that needs to be considered for dietary treatments
- C o g n i t i v e a n d b e h a v i o r a l i m p a i r m e n t i n m i l d hyperphenylalaninemia
- Prevalence and seasonal distribution of viral etiology of respiratory tract infections in inpatients and outpatients of the pediatric population: 10 year follow-up
- Evaluation of pediatric patients with an oncologic emergency: Single center experience
- Complications of cardiac catheterization in children with congenital heart disease
- Association of lactate/albumin ratio level to organ failure and mortality in severe sepsis in a pediatric intensive care unit in Egypt
- Evaluating the basic life support knowledge among schoolteachers: A cross-sectional survey in Kayseri, Turkey
- Home accident or physical abuse: Evaluation of younger children presenting with trauma, burn and poisoning in the Pediatric Emergency Department
- Evaluation of left ventricular functions with two-dimensional speckle-tracking echocardiography (2D-STE) and N-terminal ProBNP in diabetic children
- Respiratory viral infection’s frequency and clinical outcome in symptomatic children with cancer: A single center experience from a middle-income country
- Rotavirus gastroenteritis-associated urinary tract calculus in an infant
- Does inhaled salbutamol before surfactant therapy have any beneficial effect?
- A case of aquagenic syringeal acrokeratoderma with involvement of periungual area of the hand
- A patient heterozygous for R92Q mutation with periodic fever and aphthous stomatitis, pharyngitis, and adenitis (PFAPA) syndrome-like phenotype
- A child with idiopathic facial aseptic granuloma
- Secondary hemophagocytic lymphohistiocytosis in a child with Leptospira infection: A case report
- Prevalence and severity of malnutrition in pediatric neurology outpatients with respect to underlying diagnosis and comorbid nutrition and feeding related problems
- Togetherness of Ebstein anomaly and giant hairy nevus in a neonate: first case in the literature
- Aneurysmal bone cyst in the inferior nasal turbinate in a pediatric patient: A case report
- Clinical manifestations in trisomy 9 mosaicism
- Safety of subcutaneous allergen immunotherapy in children: A retrospective review and bird eye to literature
- A rare case of cephalothoracopagus janiceps conjoined twins
- A case series of hematohidrosis: A puzzling medical phenomenon
- Management of NSAID-related pyloric obstruction in a child using endoscopic balloon dilatation: A case report
- A rare cause of fatal cardiac arrhythmia: Inhalation of butane gas
- Primary cutaneous lymphoma in children: A report of four cases
- Posttraumatic stress disorder symptoms in children exposed to circumcision under general or local anesthesia
- Tufted angioma arising at the site of hepatitis B vaccination: A case report
- Percutaneous retrieval of umbilical vein catheter fragment in an infant two months after embolization
- Pulmonary artery sling anomaly presenting with unilateral lung hyperinflation: A case report
- The first pediatric case of leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL) from Turkey
- Ogilvie syndrome presenting with septic shock
- Low hemoglobin A1c levels in a patient with diabetic ketoacidosis: Fulminant type 1 diabetes mellitus
- Stuck tunneled central venous catheters in children: Four cases removed by angiography assistance
- The stress levels of parents of premature infants and related factors in Nenoatal Intensive Care Units
- Association of dysglycemia with mortality in children receiving parenteral nutrition in pediatric intensive care unit
- Acute pancreatitis in children: A single center experience over ten years
- A rare cause of neonatal hypertension: Congenital mesoblastic nephroma
- Evaluation of Restless Legs syndrome and growing pains in children with familial Mediterranean fever
- Speech delay in toddlers: Are they only “late talkers”?
- Acute renal failure due to severe hypercalcemia and nephrocalcinosis treated with two doses of pamidronate in an infant with Williams-Beuren syndrome
- Frequency of thiopurine S-methyltransferase gene variations in Turkish children with acute leukemia
- Corticosteroid phobia among parents of asthmatic children
- A “glue sniffer” teenager with anuric renal failure and hepatitis
- Reliability of ultrasonography and the Alvarado scoring system in acute appendicitis
- Positional installation of contrast (PIC) and Redo-PIC cystography for diagnosis of occult vesicoureteral reflux
- Comparison between high-flow nasal oxygen cannula and conventional oxygen therapy after extubation in pediatric intensive care unit
- Apolipoprotein E allelic variants and cerebral palsy
- Radiological nodule behavior: A critical parameter in the surgical management of pediatric pulmonary metastases
- Measuring awareness about child abuse and neglect: Validity and reliability of a newly developed tool-child abuse and neglect awareness scale
- Evaluation of autonomic nervous system functions in frame of heart rate variability in children with inflammatory bowel disease in remission
- A rare cause of facial nerve palsy in a young infant: Kawasaki disease
- Chylous ascites after lymphadenectomy in a Wilms’ tumor patient
- Is the BCS1L variant c.232A>G truly responsible for a GRACILE-like condition?
- Determinants of childhood diarrhea among under-five year old children in Nigeria: A population-based study using the 2013 demographic and health survey data
- Changes of primary headache related white matter lesions in pediatric patients
- Oral health status in patients with mucopolysaccharidoses
- Perfusion index and pleth variability index in the first hour of life according to mode of delivery
- A novel Y160C mutation of Keratin 10 gene in a Chinese male infant with epidermolytic hyperkeratosis
- Doxylamine succinate overdose: Slurred speech and visual hallucination
- Autism spectrum disorder and beta thalassemia minor: A genetic link?
- An asthmatic child with allergic bronchopulmonary aspergillosis (ABPA)
- Changes in trajectories of physical growth in a domestic adoptees sample: A preliminary study
- Foot hexadactyly, social implications and management in the African setting: Case report
- Percutaneous embolization of congenital portosystemic venous shunt in an infant with respiratory distress
- The association between monosymptomatic enuresis and allergic diseases in children
- Venous thromboembolism in two adolescents with Down syndrome
- Aluminum exposure in premature babies related to total parenteral nutrition and treatments
- Response to ''Is the BCS1L variant c.232A>G truly responsible for a GRACILE-like condition?''
- Focusing on the clinical diagnosis and risk of hairy polyp: A report of 7 cases
- Outbreak of varicella in preschool children despite one-dose vaccination
- Restless leg syndrome in children with celiac disease
- Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region
- Acute peripheral facial paralysis following varicella infection: An uncommon complication
- Investigation of the frequency of iron insufficiency among infants in a population in which routine iron supplementation is implemented
- Phenytoin induced dystonia
- Multiple cranial nerve schwannomas and meningiomas as a hallmark sign of neurofibromatosis type 2 in a child
- Hemolytic uremic syndrome and IgA nephropathy in a child: Coincidence or not?
- Anauxetic dysplasia: A rare clinical entity
- A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings
- Transcatheter retrieval of embolized catheter using venovenous loop in a neonate
- Psychiatric morbidity and quality of life in children and adolescents with cystic fibrosis
- Allergen variability and house dust mite sensitivity in pre-school children with allergic complaints
- The value of nasopharyngeal aspirate, gastric aspirate and bronchoalveolar lavage fluid in the diagnosis of childhood tuberculosis
- Assessment of central venous catheterization and complications in a tertiary pediatric intensive care unit
- Knowledge levels related to allergen specific immunotherapy and perspectives of parents whose children were diagnosed with asthma and/or allergic rhinitis in Turkey
- Clinical and molecular evaluation of 16 patients with Rett syndrome
- A rare reason in a child with feeding intolerance: Intravaginal struvite stone
- C1q nephropathy among children with nephrotic syndrome: Ten-year experience from a pediatric nephrology unit
- High frequency oscillatory ventilation versus conventional mechanical ventilation in pediatric acute respiratory distress syndrome: A randomized controlled study
- Evaluation of surgically treated breast masses in children
- Left upper lobe atelectasis due to plastic bronchitis
- Comparison of weight estimation methods and evaluation of usability of Broselow Luten tape in Turkish children
- A case report of a 4-year-old child with glucose-6-phosphate dehydrogenase deficiency: An evidence based approach to nutritional management
- Persistent hyperglycemia in a neonate: Is it a complication of therapeutic hypothermia?
- Unilateral pityriasis rosea in a child: A rare clinical presentation
- The use of nasal trumpet as a non-invasive treatment method in congenital nasal stenosis
- Association of STAT4 gene single nucleotide polymorphisms with Iranian juvenile-onset systemic lupus erythematosus patients
- Rational drug use for acute bronchiolitis in emergency care
- A pheochromocytoma case diagnosed as adrenal incidentaloma
- Isolated thoracoschisis: Case report
- Truncus arteriosus with double aortic arch: A rare association
- Non-suicidal self-injury behaviors’ features and relationship with adolescents’ daily life activities and mental status
- Incidence, risk factors and treatment outcomes of drug extravasation in pediatric patients in China
- Successful treatment of a childhood synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) syndrome with subcutaneous methotrexate: A case report
- Low serum IGF-1 and increased cytokine levels in tracheal aspirate samples are associated with bronchopulmonary dysplasia
- The long-term neurodevelopmental outcomes of infants born full-term with low birth weight
- SNAPPE-II and risk of neonatal morbidities in very low birth weight preterm infants
- Drug reaction with eosinophilia and systemic symptoms in a child on multiple antiepileptics
- The seizure semiology consistent with frontal lobe symptomatogenic zone in children
- Evaluation of complicated and uncomplicated parapneumonic effusion in children
- Complete androgen insensitivity syndrome associated with bilateral sertoli cell adenomas and unilateral paratesticular leiomyoma: A case report
- A celiac case mimicking mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)
- Parapharyngeal giant ganglioneuroma with multifocal bone involvement in a pediatric female patient
- Low pertussis antibody levels in maternal and umbilical cord blood samples in Turkey
- Establishing reference values for amplitude-integrated electroencephalography in preterms below 35 weeks of gestational age: A prospective observational cohort study
- A case of Langerhans cell histiocytosis mimicking child abuse
- Familial mutation in Caffey disease with reduced penetrance: A case report
- Treatment of a patient with Kawasaki disease associated with selective IgA deficiency by continuous infusion of cyclosporine A without intravenous immunoglobulin
- A Turkish BCS1L mutation causes GRACILE-like disorder
- Change of Helicobacter pylori prevalence in a decade among children undergoing endoscopy
- Complications with rotavirus: A single center experiences
- Type of setting for the inpatient adolescent with an eating disorder: Are specialized inpatient clinics a must or will the pediatric ward do?
- Increasing vitamin D deficiency in children from 1995 to 2011
- Association between maternal depression and wheezing in preschool children
- Fibrous hamartoma of infancy: A case report with typical ultrasonographic findings
- Response to cimetidine in a 1-year-old child with PFAPA syndrome
- Recognizing immunodeficiency in children with recurrent infections: What are the predictive factors?
- Fonsecaea pedrosoi: rare cause of dental infection and maxillary osteomyelitis in child with acute lymphoblastic leukemia
- The subclinical effect of celiac disease on the heart and the effect of gluten-free diet on cardiac functions
- Mental health problems in children with uncomplicated epilepsy; relation with parental anxiety
- Gender differences in defense mechanisms, ways of coping with stress and sense of identity in adolescent suicide attempts
- Is white matter affected in adolescents with anorexia nervosa? A study using magnetization transfer imaging
- Accidental cisplatin overdose in a child: Successful management with repetitive plasmapheresis and use of chemoprotective agents
- The need for mechanical ventilation in a child exposed to a laundry detergent pod
- Infectious diseases, autoimmunity and midline defect in patient with novel bi-allelic mutation in IL12RBI gene
- Neuromyelitis optica mimics the morphology of spinal cord tumors
- Pediatric bladder/prostate rhabdomyosarcoma: Eight cases from a single center
- Nail changes secondary to hand-foot-mouth disease
- Severe theophylline poisoning treated with continuous venovenous hemodialysis in a child
- Familial Mediterranean fever associated with optic neuritis, successfully treated with anti-interleukin 1 agents
- Neurological findings spectrum in Celiac disease
- "Silent" ?-thalassemia mutation (promoter nt-101 C > T) with increased hemoglobin A2
- Fatal paraphenylenediamine poisoning due to black henna
- Occurrence of paratubal cysts in childhood: An analysis of 26 cases
- Pulmonary vascular anomalies: a review of clinical and radiological findings of cases presenting with different complaints in childhood
- A late-diagnosed phenylketonuria case presenting with autism spectrum disorder in early childhood
- Attention deficit hyperactivity disorder and other disruptive behavior disorders are risk factors for recurrent epistaxis in children: A prospective case-controlled study
- Serum IL-13 levels at diagnosis and remission in children with malignant lymphoma
- Screening 5 and 6 year-old children starting primary school for development and language
- Are the methylenetetrahydrofolate reductase 1298 and 677 gene polymorphisms related to optic glioma and hamartoma risk in neurofibromatosis type 1 patients?
- Prepubertal vaginal discharge: Vaginoscopy to rule out foreign body
- Congenital malaria: Importance of diagnosis and treatment in pregnancy
- Effects of physiotherapy combined with sirolimus in a patient with vascular malformation: A case report
- Nasal chondromesenchymal hamartoma, a rare pediatric tumor: Case report
- Ceftriaxone-induced hemolytic anemia in a child successfully managed with intravenous immunoglobulin
- Successful treatment of refractory listeria meningitis and bacteremia with trimethoprim-sulfamethoxazole in an immunocompetent child
- An unexpected diagnostic course of systemic lupus erythematosus
- Horseshoe kidney with growth retardation: Don't forget Turner syndrome
- Aberrant cervical thymus and the role of ultrasonography: A case report
- Carotid intima-media thickness and arterial stiffness as early markers of atherosclerosis in pediatric celiac disease
- Clinical accuracy of non-contact infrared thermometer from umbilical region in children: A new side
- Serum vitamin D levels during activation and remission periods of patients with juvenile idiopathic arthritis and familial Mediterranean fever
- Horseshoe kidney with growth retardation: Don't forget Turner syndrome
- Evaluation of the removal reasons of totally implantable venous devices in children: a retrospective study
- Parotidectomy outcomes, diagnosis and complications on pediatric patients; Twelve years of experiences in a tertiary care center
- Venlafaxine intoxication in an adolescent presenting with severe lactic acidosis
- Different clinical spectrum of leptospirosis
- Functional outcomes of mandibular distraction for the relief of severe airway obstruction and feeding difficulties in neonates with Pierre Robin sequence
- Stepwise diet management in pediatric gastrointestinal graft versus host disease
- Is anti-Mullerian hormone an indicator of potential polycystic ovary syndrome in prepubertal girls with simple obesity?
- Kawasaki disease shock syndrome: a rare and severe complication of Kawasaki disease
- Genotypic and phenotypic features of the cystinosis patients from the South Eastern part of Turkey
- Clarithromycin resistance and 23S rRNA gene point mutations of Helicobacter pylori infection in children
- Oxygen therapy via high flow nasal cannula in pediatric intensive care unit
- Local hypertrichosis: A rare complication of a temporary henna tattoo
- Two newborn babies with generalized arterial calcification of infancy, two new mutations
- Multisystem langerhans cell histiocytosis with thymic involvement diagnosed with anterior mediastinal mass in a 2-month-old boy
- Surgical and clinical strategies in the management of thyroid medullary carcinoma in children with and without ret proto- oncogene mutations
- An unusual manifestation: Papillary thyroid carcinoma in a patient with ataxia-telengiectasia
- A case with atrophic autoimmune thyroiditis-related hypothyroidism causing multisystem involvement in early childhood
- Intravesical catheter knotting: an unusual complication of suprapubic catheterization
- Transient tachypnea of the newborn: are there bedside clues for predicting the need of ventilation support?
- Clinical and genetic features of IL12Rb1 deficiency: Single center experience of 18 patients
- Pediatric langerhans cell histiocytosis: single center experience over a 17-year period
- Anti-cyclic citrullinated peptide antibodies are not frequently observed in children with type 1 diabetes mellitus: a single- center study
- The first childhood case with coexisting Hashimoto thyroiditis, vitiligo and autoimmune hepatitis
- Idiopathic giant cell myocarditis in a newborn: case report
- Reliability of cerebral oximeter in non-invasive diagnosis and follow-up of hypercapnia
- Efficacy of asthma education program on asthma control in children with uncontrolled asthma
- Consensus statement on diagnosis, treatment and follow-up of cow’s milk protein allergy among infants and children in Turkey
- Changing epidemiology of non-cystic fibrosis bronchiectasis Original
- High frequency of pertussis in older children and adolescents with prolonged cough in Turkey
- Predictors of self-esteem in adolescents with a psychiatric referral
- Diagnosis of cystic fibrosis with chloride meter (Sherwood M926S chloride analyzer®) and sweat test analysis system (CFΔ collection system®) compared to the Gibson Cooke method
- Long term azithromycin therapy in patients with cystic fibrosis
- The comparison of general movements assessment and neurological examination during early infancy
- Associations of lean and fat mass measures with whole body bone mineral content and bone mineral density in female adolescent weightlifters and swimmers
- An unusual case of neuroblastoma: a 17-year-old adolescent presented with bilateral diffuse lung metastasis at initial diagnosis
- A novel mutation in a case of pseudohypoparathyroidism type Ia
- Neonatal lupus erythematosus: Report of a case with cutaneous, hematological and hepatobiliary findings
- Neck epidermoid cyst mimicking tuberculosis at ultrasound: Case report and review of literature
- Severe hyperphosphatemia after oral laxative administration in a 7-year-old patient
- Recessive congenital methemoglobinemia in immediate generations
- Late-diagnosed phenylketonuria in an eight-year-old boy with dyslexia and attention-deficit hyperactivity disorder
- A novel de novo mutation involving the MLL2 gene in a Kabuki syndrome patient presenting with seizures
- An unusual complication of endotracheal intubation: ingestion of a bulb in a premature neonate
- Microorganisms isolated from cultures and infection focus and antibiotic treatments in febrile neutropenic children from Şanlıurfa, Turkey
- A pediatric case of Fascioliasis with eosinophilic pneumonia
- Evaluation of central nervous system in patients with glycogen storage disease type 1a
- Parental perception and child’s nutritional status Original
- A new emerging problem in pediatric emergency units: Synthetic cannabinoids
- Increased mean platelet volume in children with sepsis as a predictor of mortality
- Paracetamol infusion-related severe hypotension and cardiac arrest in a child
- Corynebacterium propinquum bronchopneumonia in a child with ataxia telangiectasia
- Rosai-Dorfman disease of vertebra: Case report and literature review
- The efficacy and safety of naproxen in acute rheumatic fever: The comparative results of 11-year experience with acetylsalicylic acid and naproxen
- Hepatitis A virus epidemiology in Turkey as universal childhood vaccination begins: seroprevalence and endemicity by region
- Cerebrovascular complication of infective endocarditis complicated with abdominal trauma
- Asthma control test and pediatric asthma quality of life questionnaire association in children with poor asthma control
- Waist to height ratio: a simple screening tool for nonalcoholic fatty liver disease in obese children
- Factors affecting survival in neonatal surgery unit in a tertiary care university hospital during 26 years
- Bone marrow aspiration complications: Iliopsoas abscess and sacroiliac osteomyelitis
- Gonadoblastoma in a patient with 46, XY complete gonadal dysgenesis
- Coexistence of early onset sarcoidosis and partial interferon-? receptor 1 deficiency
- Cardiac nodal and cardiac autonomic functions in children with vasovagal syncope
- Peutz-Jeghers syndrome: an unusual cause of recurrent intussusception in a 7-year-old boy
- Comparison of risk scoring systems in congenital heart surgery
- Detection of gastroesophageal reflux in children with cerebral palsy using combined multichannel intraluminal impedance- ph procedure
- Seizures and diagnostic difficulties in hyperinsulinism- hyperammonemia syndrome
- Primary intrarenal neuroblastoma in a 13-month-old girl presenting as a Wilms' tumor with pulmonary metastasis
- Aspartate aminotransferase-to-platelet ratio index in children with cholestatic liver diseases to assess liver fibrosis
- Importance of neurologic and cutaneous signs in the diagnosis of Schimke immuno-osseous dysplasia
- Systemic onset juvenile idiopathic arthritis with macrophage activation syndrome and coronary artery dilatation misdiagnosed as Kawasaki disease
- A rare hydrocephalus complication: cortical blindness
- Hypersensitivity pneumonia in a schoolchild admitted to the hospital's asthma clinic
- Can Burkitt's Lymphoma and Hodgkin's Lymphoma occur in siblings simultaneously?
- Pediatric tuberculosis in Turkey: a review of 8-years period in a tertiary care hospital
- Development of a screening tool for children's growing pains: validation, reliability control and clinical evaluation
- Total oxidant status, total antioxidant capacity and ischemia modified albumin levels in children with celiac disease
- A case of hyperkinetic movement disorder associated with LGI1 antibodies
- DRESS syndrome presents as leukoencephalopathy
- Childhood epilepsy with occipital paroxysm: classification, atypical evolution and long-term prognosis in 35 patients
- Bonzai intoxication in children: our experience with 17 cases
- Clinical features and treatment results in children with anaplastic large cell lymphoma
- Prolonged pacifier usage in infancy does not cause eating behavior problem later
- The perceptions of pediatricians regarding their self-efficacy in child neglect and abuse
- A rare but important adverse effect of tacrolimus in a heart transplant recipient: diabetic ketoacidosis
- Empiric treatment of children with gastroesophageal reflux- like symptoms: Effect of proton pump inhibitors
- Clinical and neuroradiologic variability of Aicardi-Goutiéres syndrome: Two siblings with RNASEH2C mutation and a boy with TREX1 mutation
- Hypersensitivity pneumonia in a schoolchild admitted to the hospital's asthma clinic
- Development of a screening tool for children's growing pains: validation, reliability control and clinical evaluation
- A presentation of Lyme disease: pseudotumor cerebri
- Meriç Kaymak-Cihan1, Olcay Kandemir2, Klara Dalva3, Neriman Sarı4, Nilgün Kurucu4, İnci Ergürhan-İlhan4
- A 7-year study of the distribution of nosocomial candidemia in children with cancer
- An aggressive parenteral nutrition protocol improves growth in preterm infants
- Platelets and platelet-derived growth factor in closure of the ductus arteriosus
- Determination of Helicobacter pylori antibiotic resistance patterns in pediatric gastroenterology patients: the Hacettepe experience
- Risk factors for persistence of coronary artery abnormalities in Turkish children with Kawasaki disease
- Turkish cases of early infantile epileptic encephalopathy: two novel mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene
- Molecular diagnosis of Fanconi anemia with next-generation sequencing in a case with subtle signs and a negative chromosomal breakage test
- TSEN54 gene-related pontocerebellar hypoplasia type 2 presenting with exaggerated startle response: report of two cases in a family
- A pediatric case of acute meningitis due to Streptococcus pneumoniae serotype 33D
- A giant hydatid cyst atypically located in the left ventricle
- Blue-colored sweating: four infants with apocrine chromhidrosis
- Intralobar pulmonary sequestration associated with congenital broncho-esophageal fistula
- An easily missed diagnosis: 17-alpha-hydroxylase/17,20-lyase deficiency
- Sapropterin dihydrochloride treatment in Turkish hyperphenylalaninemic patients under age four
- The prognostic role of prenatal MRI volumetric assessment in fetuses with isolated ventriculomegaly
- A new insight into food addiction in childhood obesity
- Conventional and advanced MR imaging in infantile Refsum disease
- Prevalence of and risk factors for otitis media with effusion in primary school children: case control study in Erzurum, Turkey
- Chanarin–Dorfman syndrome: a novel mutation in a Turkish girl
- Evaluation of the likelihood of reflux developing in patients with recurrent upper respiratory infections, recurrent sinusitis or recurrent otitis seen in ear-nose-throat outpatient clinics
- Human herpesvirus 6 infection mimicking measles: two pediatric cases
- Idiopathic central diabetes insipidus presenting in a very low birth weight infant successfully managed with lyophilized sublingual desmopressin
- Angiomatoid fibrous histiocytoma: case report and review of the literature
- Spasmodic torticollis associated with sertraline in a child and an adolescent
- Circulating fibroblast growth factor 23 in children on peritoneal dialysis is associated with effective dialysis
- Association between teething and independent walking in healthy children
- Chronic lip swelling as the sole presentation of Crohn’s disease: three case reports
- Primary laryngeal lymphoma in a child
- Datura stramonium poisoning in a child
- Resolution of food-induced anaphylaxis in DOCK8-deficient patients following bone marrow transplantation
- The effect of gynecomastia on body image perception and gender roles in adolescents
- Two cases of hereditary benign telangiectasia in Turkey: sporadic occurrence with punctate telangiectasias surrounded by anemic- halos
- Mannose-binding lectin may affect pregnancy outcome
- Tuberculous liver abscess in an immunocompetent child with pulmonary tuberculosis as a cause of fever of unknown origin
- Brainstem auditory evoked potentials in late preterm infants at term-equivalent age
- Neonates with inborn errors of metabolism: spectrum and short-term outcomes at a tertiary care hospital
- Acute lobar nephronia: value of unique magnetic resonance imaging findings in diagnosis and management
- Early or later prophylactic INSURE in preterm infants of less than 30 weeks’ gestation
- Decreased bone ultrasound velocity in premature infants conceived with assisted reproduction
- Parental perceptions concerning the effect of center-based childcare on quality of life for healthy 2- to 4-year-old children
- Eight different viral agents in childhood acute gastroenteritis Original
- Semiological seizure classification of epileptic seizures in children admitted to video-EEG monitoring unit
- Systems-level analysis of genome wide association study results for a pilot juvenile idiopathic arthritis family study
- Atypical clinical manifestations of hepatitis a among children aged 1-16 years in South-Eastern Region of Turkey
- Incidence and follow-up outcomes of developmental hip dysplasia of newborns in the Western Mediterranean Region
- A neonate with intestinal volvulus without malrotation exhibiting early jaundice with a suspected fetal onset
- Cetirizine and albendazole induced dystonia in a child
- Predictive factor for first wheezing episode
- Embolization of a complex pulmonary arteriovenous fistula and coarctation treatment with covered stent at the same session
- Prognostic factors and treatment results of pediatric Hodgkin's lymphoma: A single center experience
- Pyloric atresia-junctional epidermolysis bullosa syndrome showing novel c.4505-4508insACTC mutations in integrin b4 gene (ITGB4)
- Acute colchicine intoxication complicated with complete AV block
- A case of xanthogranulomatous pyelonephritis mimicking Wilms tumor
- Early rehabilitation of a child with intensive care unit acquired weakness secondary to membranoproliferative glomerulonephritis: A case report
- Is compliance with gluten-free diet sufficient? Diet composition of celiac patients
- Prognostic factors and treatment results of pediatric Hodgkin's lymphoma: A single center experience
- Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation
- Optic neuritis as a presenting symptom of Mycoplasma pneumoniae infection
- Serum vitamin B12, folic acid, and homocysteine levels in children with febrile seizure
- Pyridoxine-dependent epilepsy in two Turkish patients in Turkey and review of the literature
- Comparison of risk factors in newborn hearing screening in a developing country
- Clinical features and long-term outcomes of idiopathic urethrorrhagia
- Scientific publications in pediatrics over the last ten years in Turkey and worldwide
- Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities
- A lethal danger in the home: turpentine poisoning
- ST-segment elevation following lightning strike: case report and review of the literature
- A rare case of primary inoculation tuberculosis seen after varicella
- Occurrence of Wilms' tumor in a child with hereditary spherocytosis
- Autologous cord blood transplantation in neuroblastoma
- Evaluation of childhood brucellosis in the central Black Sea region
- Postmortem clinical examination by experienced clinical geneticists as an alternative to conventional autopsy for assessment of fetal and perinatal deaths in countries with limited resources
- Toilet training age and influencing factors: a multicenter study
- Intractable colitis associated with chronic granulomatous disease in a young girl
- Report of a case of neonatal chylothorax that responded to long-term octreotide treatment, and review of the literature
- A newborn with trisomy 13 presenting with cloacal exstrophy
- Simultaneous presentation of malignant peripheral nerve sheath tumor and moyamoya disease associated with neurofibromatosis type 1 in a child
- Ocular morbidities of premature children with mild or no retinopathy of prematurity
- Interventional cardiac catheterization in infants weighing less than 2500 g
- Polymorphisms in FAS and CASP8 genes may contribute to the development of ALPS phenotype: a study in 25 patients with probable ALPS
- Comparison of the BD GeneOhm VanR assay and a chromogenic agar-based culture method in screening for vancomycin-resistant enterococci in rectal specimens of pediatric hematology-oncology patients
- Occurrence of Wilms' tumor in a child with hereditary spherocytosis
- Cardiac thrombus developing after an accidental high-voltage electric shock in a child
- Evaluation of late effects of postoperative radiotherapy in patients with medulloblastoma
- Melanotic neuroectodermal tumor of infancy in the skull: a case report
- Early-term delivery and adverse neonatal outcomes at a tertiary center in Turkey
- Late preterm infants: Week by week outcomes of morbidity and mortality
- Acute tubulointerstitial nephritis: a case series and long- term renal outcomes
- Physical activity intensities during school time in healthy prepubertal boys and BMI
- Sinus tachycardia related to tacrolimus after kidney transplantation in children and young adults
- Celiac disease in patients with Williams-Beuren syndrome
- The first case of Raoultella terrigena infection in an infant
- Epidermal cyst in the patent processus vaginalis: An unusual inguinal mass in a girl
- Celiac disease, phylloid hypomelanosis and autoimmune thyroiditis: a case report
- Reply
- Hereditary benign telangiectasia?
- Antenatal hydronephrosis: a single center’s experience and follow-up strategies
- Panton-Valentine leukocidin positive Staphylococcus aureus infection in childhood: a case report
- Rare vascular pathology sinus pericranii; becomes symptomatic with pseudotumor cerebri
- Late presentation of congenital diaphragmatic hernia
- Did the child have fever of unknown origin?
- Hereditary benign telangiectasia Response to "Letter to the editor" by Ozsoylu entitled "Hereditary benign telangiectasia?"
- Aspiration of an interesting foreign body: Myiasis
- The importance of physical examination findings and the use of physostigmine
- Transient hypogammaglobulinemia of infancy: predictive factors for late recovery
- Testicular cavernous hemangioma presenting as an ipsilateral lesion in a child with multicystic dysplastic kidney
- The relation between mean platelet volume and mortality in critical pediatric patients
- A fatal case caused by massive honey bee stings
- Unilateral nevoid telangiectesia: report of two pediatric cases
- Comparison of endotracheal aspirate and non-bronchoscopic bronchoalveolar lavage in the diagnosis of ventilatorassociated pneumonia in a pediatric intensive care unit
- Breast milk Beta-glucuronidase levels in hyperbilirubinemia
- A case with some clinical findings overlapping to Rubinstein-Taybi, Rubinstein-Taybi-like syndrome or multiple pterygium syndrome: Coincidental findings or a new entity
- Molecular genetic analyses of cystinuria type 1 in 24 turkish patients
- Cutis marmorata telangiectatica congenita. An unusual cause of lower extremity hypoplasia
- Subadventitial hematoma of a patent ductus arteriosus and thrombus formation within the aorta secondary to cardiac catheterization
- Seroprevalence of Helicobacter pylori in a pediatric population
- Central nervous system involvement of polyarteritis nodosa: A case report
- Lupus anticoagulant and protein S deficiency in a child who developed disseminated intravascular coagulation in association with varicella
- Dermatomyositis with membranous nephropathy
- Chronic idiopathic neutropenia associated with gingival enlargement
- A practical GnRH analogue (triptorelin) stimulation test to distinguish constitutional delay of puberty from hypogonadotropic hypogonadism in prepubertal boys
- Fluoride content of infant formulas and market milk in Turkey
- Unilateral late-onset tibia vara associated with bilateral proximal femoral growth disturbance in monozygotic twins: Case report
- Rapidly progressive bronchiectasis complicating ulcerative colitis in a child
- Serum ferritin, iron levels and iron binding capacity in asymmetric SGA babies
- Bleomycin-induced hyperpigmentation and hypersensitivity reactions to etoposide and vinblastine in a child with endodermal sinus tumor.
- Monotherapy with meropenem versus combination therapy with piperacillin plus amikacin therapy for neutropenic fever in children with lymphoma and solid tumors
- Combined use of chemotherapy and 131 I-metaiodobenzylguanidine in the treatment of advanced-stage neuroblastoma.
- MR imaging of pelvic and thigh muscles in congenital muscular dystrophy
- Chronic inflammatory bowel disease in a patient with common variable immunodeficiency
- Pediatricians' opinions about the problems between the departments of pediatrics and child psychiatry and possible solutions
- The role of pulmonary artery anatomy in repair of tetralogy of fallot
- Antenatal diagnosis of postductal coarctation of the aorta: A case report
- The de Barsy syndrome
- HLAs in children with minimal change disease and other types of nephrotic syndrome in the Southern Part of Turkey
- Diastolic forward blood flow in the pulmonary arteries of normal children: A Doppler echocardiographic study
- Transcatheter closure of secundum atrial septal defects, a ventricular septal defect, and a patent arterial duct
- Prevalence of asthma-associated symptoms in Turkish children
- Noninvasive diagnosis and surgical management in total anomalous pulmonary venous return draining into the coronary sinus: Report of 2 cases
- Systemic lupus erythematosus presenting with generalized lymphadenopathy : A case report
- Henna-induced hemolytic anemia and acute renal failure
- Pseudohypoparathyroidism type IA and II with severe neuropsychic manifestations
- Endovascular stent implantation in congenital heart defects
- Screening for tuberculosis in a primary school in Ankara
- Assessment of protein-energy malnutrition in children with chronic arthritis
- Anomalous origin of one pulmonary artery branch from ascending aorta ("so-called hemitruncus"): report of an additional case treated surgically.
- Gaucher disease type I: Analysis of two cases with thalassemic facies and pulmonary arteriovenous fistulas
- Complex partial seizure mimicking psychotic reaction in an adolescent
- The impact of pre-and perinatal factors on attention-deficit and disruptive behavior disorders
- Overdiagnosis of pneumonia in children
- Thoracoschisis associated with diaphragmatic hernia in a 31-week-old stillbirth
- A case of osteopetrosis with pelvic ectopic spleen: An unusual association
- Preliminary pediatric transesophageal echocardiography experiences
- Socioeconomically advantaged infants attending a university well-child clinic in Ankara: Are they breast-feeding optimally
- Fiberoptic flexible bronchoscopy via the laryngeal mask airway in children
- A case of Netherton's syndrome with cerebral infarction.
- Noncompaction of the right ventricle following Senning repair
- Abetalipoproteinemia: A case report
- Bilateral subpleural ectopic brain tissue in a 23-week-old fetus
- Complications of the two major operations of Hirschsprung's disease: a single center experience
- Megakaryocyte emperipolesis in a child with chronic neutropenia: An unusual coexistence
- Serum lipid peroxidation levels in small-for-gestational-age babies
- Prevalence of asthma and other allergic disorders among schoolchildren in Diyarbakır, Turkey
- A study of the prevalence of having fractures and the affecting factors in young male adults throughout chiidhood and adolescence
- Two male patients with nevoid basal cell carcinoma syndrome from Turkey
- Prenatal echocardiographic diagnosis of situs inversus totalis and transposition of the great arteries: A case report
- Pulmonary arteriovenous fistula in the newborn: A case report of Rendu-Osler-Weber syndrome and a review of the literature
- Atrial septal aneurysm in children
- A new case of Balci's syndrome (corneal opacity, microphthalmia, microcephaly, mental retardation, and generalized muscular spasticity associated with congenital heart disease).
- A case of Sandifer's syndrome with hand tremor
- Estimation of pulmonary artery pressure by contrast-enhanced Doppler signals and comparison with catheter-measured pressures
- The role of heterotopic gastric mucosa with or without colonization of Helicobacter pylori upon the diverse symptomatology of Meckel's diverticulum in children.
- Fiberoptic phototherapy versus conventional daylight phototherapy for hyperbilirubinemia of term newborn
- Giant cell pneumonia in a leukemic child in remission: A case report
- Severe hemolytic anemia after repair of primum septal defect and cleft mitral valve
- Familial arthropathy with camptodactyly: Reports of two families
- Height prognosis in children with late-diagnosed congenital hypothyroidism
- Intraperitoneal involvement in rhabdomyosarcoma CT findings in a child
- Low plasma apolipoprotein A-I level: New prognostic criterion in childhood cirrhosis
- Familial microtia in four generations with variable expressivity and incomplete penetrance in association with type I syndactyly
- An open trial and discontinuation study of fluoxetine in children and adolescents with obsessive-compulsive disorder
- Hodgkin's disease and renal paraneoplastic syndromes in childhood
- Arylsulfatase a pseudodeficiency incidence in Turkey
- Occurrence of an aortic arch anomaly in two siblings born to a diabetic mother
- Intermediate-term follow-up results of pulmonary balloon valvuloplasty in children
- Clinical trial to evaluate immunogenicity and safety of inactivated hepatitis A vaccination starting at 2-month-old children
- Prune-belly syndrome associated with extra-abdominal abnormalities in a 7-year-old boy
- Asplenia in a patient with Fanconi's anemia-like congenital aplastic anemia
- Pulmonary hemosiderosis with juvenile rheumatoid arthritis: A case report
- Salmonella septic arthritis in a patient with acute idiopathic thrombocytopenic pupura treated with steroid
- Are the stool characteristics of preterm infants affected by infant formulas ?
- A case of primary chylous ascites resolved within 4 months by exclusive breast-feeding
- Juvenile rheumatoid arthritis presented with thrombocytopenia
- Alternative diagnostic method for streptococcal pharyngitis: Breese scoring system
- Drug-resistant tuberculosis in Turkish children
- Triplets with growth failure, microcephaly, mental retardation, nail hypoplasia and corpus callosum agenesis: Is it a variant of Coffin-Siris or a new syndrome?
- Alimentary tract duplications in children: Report of 26 years' experience
- Poststreptococcal reactive arthritis: Clinical course and outcome in 15 patients
- Allogeneic bone marrow transplantation for children with myelodysplastic syndrome
- Juvenile hyaline fibromatosis in one Turkish child
- Dual-probe pH monitoring for the assessment of gastroesophageal reflux in the course of chronic hoarseness in children
- Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome) in a Turkish child
- Thoracic ectopic kidney in a child: A case report
- Acute lymphoblastic leukemia in a child with Wilson disease
- Serratia marcescens: An emerging microorganism in the neonatal intensive care unit
- Hemophilic arthropathy: Evaluation of clinical and radiological characteristics and disability
- Polymorphisms of surfactant protein A genes and the risk of bronchopulmonary dysplasia in preterm infants
- Ivemark syndrome: Asplenia with kidney collecting duct cysts and polysplenia with cerebellar cyst
- Ventricular diastolic filling indices in pulmonary stenosis
- Body stalk anomaly in monozygotic twinning: A case report
- Fludarabine, cytarabine, G-CSF and idarubicin (FLAG-IDA) for the treatment of relapsed or poor risk childhood acute leukemia
- A case of isotretinoin embryopathy with bilateral anotia and Taussig-Bing malformation
- Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations
- Unguarded tricuspid orifice diagnosed by echocardiography: A clinical study
- Teratoid Wilms' tumor: A case report
- Biphasic pulmonary blastoma in a child
- Hereditary angioedema: Case report of a family
- Clinical features of 21 patients with lissencephaly type I (agyria-pachygyria)
- Preoperative diagnosis of bronchial atresia presenting with recurrent respiratory symptoms in an infant
- Intraabdominal lymphangiomyoma in an infant with protein-losing enteropathy and hemihypertrophy
- Reactogenicity and immunogicity of a new measles-mumps-rubella vaccine containing RIT 4385 mumps virus strain in healthy Turkish children
- Neonatal tetanus in the Southeast of Turkey: Risk factors, and clinical and prognostic aspects review of 73 cases, 1990-1999
- Familial müllerian agenesis
- The relationship between osteocalcin levels and sexual stages of puberty in male children
- Polysplenia syndrome with hepatic artery of superior mesenteric artery origin and a circumaortic renal vein
- Triosephosphate isomerase deficiency with elevated sweat chloride test : Report of a case
- Analysis of 2017 holter records in pediatric patients
- Complications of pediatric cardiac catheterization: 18-month study
- Dilatation of a restrictive interatrial communication using a balloon angioplasty catheter
- Thymic enlargement in childhood
- Congenital generalized infantile myofibromatosis and neonatal hemochromatosis: An autopsy case report
- Carnitinuria in rickets due to vitamin D deficiency
- Congenital sick sinus syndrome with breath holding and severe syncope episodes during infancy: A case report
- Neonatal morbidity and mortality associated with maternal HELLP syndrome
- Double meningocele: Case report
- Pseudomonas sepsis with neutrophagocytosis in a premature newborn
- The clinical outcome of childhood masturbation
- A rare coexistence of two gastric outlet obstructive lesions: Infantile hypertrophic pyloric stenosis and organoaxial gastric volvulus
- Serum levels of antioxidant vitamins (alpha tocopherol, beta carotene, and ascorbic acid) in children with bronchial asthma
- Balloon dilatation angioplasty of stenosed systemic-pulmonary artery shunts
- Malignant fibrous histiocytoma in a child (A case report and review of the literature)
- Severe lymphopenia in tuberculosis (A mere coincidence or a significant association?)
- Postoperative graft thrombosis in Fontan procedure
- Iron status in breast-fed full-term infants
- Partial splenic embolization in beta-thalassemia major : A case report
- Depression in children with hemophilic arthropathy and poliomyelitis: A preliminary report
- Neurological soft signs and EEG findings in children and adolescents with Gilles de la Tourette syndrome
- Inguinoscrotal hematocele of the newborn
- Interferon-alpha treatment for chronic hepatitis C in children
- Propranolol for primary and secondary prophylaxis of variceal bleeding in children with cirrhosis
- Solitary rectal ulcer syndrome in children
- Cyclic neutropenia complicated by renal AA amyloidosis
- Allergic bronchopulmonary aspergillosis in two patients with cystic fibrosis
- Bacterial nosocomial infections in mechanically ventilated children
- Regressed retinopathy of prematurity in children aged 5-8 years in Sivas, Turkey
- Serum levels of eosinophilic cationic protein (ECP), myeloperoxidase (MPO), lipid peroxidation products, interleukin (IL)-5 and interferon (IFN)-$gamma$ in children with bronchial asthma at acute asthma attack and remission
- Associated brain abnormalities in patients with corpus callosum anomalies
- Tropisetron in the prevention of chemotherapy-induced acute emesis in pediatric patients
- Stenotrophomonas maltophilia pneumonia in a premature infant
- Human leukocyte antigens in Turkish pediatric celiac patients
- A Turkish family with Greig cephalopolysyndactyly syndrome
- Congenital primary hypoparathyroidism presented with extensive cutaneous and subcutaneous calcifications
- Gastric perforation presenting as bilateral scrotal pneumatoceles
- Cyclosporin A plus prednisone treatment of steroid-sensitive frequently relapsing nephrotic syndrome in children
- Primary intracranial germ cell tumors in children : A report of eight cases and review of the literature
- Tracheal rupture: A rare complication related to foreign body aspiration
- Guanosine triphosphate cyclohydrolase I deficiency: A rare cause of hyperphenylalaninemia
- Cryptosporidium parvum prevalence in a group of Turkish children
- Rhabdomyosarcoma of the biliary tree
- Biphenotypic characteristics, cell size and prognosis in childhood acute myeloblastic leukemia
- Methylenetetrahydrofolate reductase (MTHFR) C677T mutation in Turkish patients with thrombosis
- Cerebrospinal fluid pleocytosis in acute lymphoblastic leukemia without central nervous system relapse: A report of three cases
- A warm antibody mediated acute hemolytic anemia with reticulocytopenia in a four-month-old girl requiring immunosuppressive therapy
- Leukocytoclastic vasculitis in a child with epidermolysis bullosa simplex
- Four different hernias are encountered in the anterior part of the diaphragm
- A case with acute leukemia presenting with cardiac tamponade
- A case of hemophilia a associated with Hodgkin's disease
- Neonatal outcome following early onset preterm premature rupture of the membranes - A case controlled study
- Congenital microvillus atrophy in a 4-month-old girl
- Cardiac dysrhythmia that simulates seizure disorder in two children
- Bronchiectasis due to ciliary aplasia in Turner's syndrome
- Relationship between high leukocyte count and cell size in childhood acute myeloblastic leukemia
- MRI of fibromatosis colli
- Serum leptin levels during childhood and adolescence: Relationship with age, sex, adiposity and puberty
- Prevalence of asthma symptoms among Turkish cypriot school children
- Neurological crisis mimicking acute pancreatitis in tyrosinemia type I
- Hemostatic system in early respiratory distress syndrome: Reduced fibrinolytic state?
- Autoimmune hemolytic anemia with warm antibodies in children: Retrospective analysis of 51 cases
- Blood levels of leukotrienes ( LTC4, D4, E4, B4 ) and synthesis of leukotriene B4 by peripheral leukocytes in children with acute A and B hepatitis
- Hepatitis as the presenting symptom of childhood systemic lupus erythematosus
- Two female siblings from Turkey with langer mesomelic dysplasia ( Homozygous Leri-Weill dyschondrosteosis syndrome )
- Psoriasis in a patient with neurofibromatosis
- CEA, CA125 and CA19-9 levels in congenital gastrointestinal anomalies
- Safety, tolerability and immunogenicity of a Haemophilus influenzae type b vaccine containing aluminum phosphate adjuvant administered at 2, 3 and 4 months of age
- Psychiatric symptoms among Turkish adolescents
- Benign rheumatoid nodules of childhood
- Sacroiliitis in familial Mediterranean fever: An unusual presentation in childhood
- Changes of hemostatic factors in patients with hemoglobinopathies
- Profile of bone marrow iron stores in childhood iron deficiency anemia
- The impact of the sexual maturation stage on body mass index in adolescent girls
- Vascular ring formed by right aortic arch with aberrant left subclavian artery and left ligamentum arteriosum: A rare cause of respiratory distress in newborn infants
- Gastric antral stricture in a patient with chronic granulomatous disease
- Fatal acidosis in a neonate with Pearson syndrome
- The accuracy of antenatal fetal echocardiography
- Percutaneus transvenous balloon mitral valvuloplasty: Mid-term results in adolescents
- Torsade de pointes associated with encephalitis
- Tumoral calcinosis ( A case report )
- Eosinophilic fasciitis-progression to linear scleroderma ( A case report )
- Neural tube defects in Turkey: Prevalence, distribution and risk factors
- Respiratory distress due to esophageal perforation caused by ball point ingestion
- Increased gastric juice leukotriene B4, C4 and E4 concentrations in children with Helicobacter pylori colonization
- Scimitar syndrome with absence of the right pulmonary artery ( A case report )
- Rh disease: Intrauterine intravascular fetal blood transfusion by cordocentesis
- Late infantile acid maltase deficiency ( A case report )
- Wilson's disease patients with normal ceruloplasmin levels
- Vascular hamartoma of the mediastinum ( A case report )
- Failure of granulocyte colony-stimulating factor and granulocyte-macrophage colony-stimulating factor in a patient with Kostmann syndrome
- An uncommon association of H-type tracheoesophageal fistula with infantile hypertrophic pyloric stenosis
- Two siblings with Bloom's syndrome exhibit different clinical features: Possible effect of sex
- Epidemiology and antibiotic resistance of gram-negative urinary pathogens in pediatric patients
- Intermittent chemotherapy for miliary tuberculosis in children
- Echocardiographic diagnosis of sinus valsalva aneurysm rupture in two pediatric patients
- Frequency of antinuclear antibodies and rheumatoid factor in healthy Turkish children
- Prevalence of GB virus C / hepatitis G virus infection in pediatric patients receiving multiple transfusions in Southern Turkey
- The evaluation of ocular trauma in children between ages 0-12
- The split notochord syndrome with dorsal enteric fistula, meningomyelocele and imperforate anus
- Identity confusion and depression in groups of adolescents having psychiatric and physical symptoms
- Cartilaginous hamartoma of the chest wall with secondary aneurysmal cyst-like areas in an infant ( A case report )
- Neonatal sublingual traumatic ulceration (Riga-Fede disease ): A case report
- Ursodeoxycholic acid therapy in children with cholestatic liver disease
- Congenital malaria ( A case report )
- A case of a four - day - old male with carpenter's syndrome with transposition of great arteries
- Lupus vulgaris secondary to single BCG vaccination ( A case report )
- İntermittent - low dose G - CSF treatment in a patient with chronic neutropenia
- Urinary calcium excretion of children living in the east region of Turkey
- Balloon atrial septostomy under echocardiographic guıdance ( Case report )
- Congenital sialidosis
- DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis
- The role of paf and leukotrienes in bioincompatibility of cuprophane membranes in hemodialysis
- Occult pneumococcal septicemia and pneumococcal pneumonia complicating pneumatoceles in a previously healthy child
- Echocardiographic assessment of left and right ventricular diastolic functions in children with dilated cardiomyopathy
- Detection of early anthracycline - induced cardiotoxicity in childhood cancer with dobutamine stress echocardiography
- Long - term follow - up of hepatitis B virus carriers with normal transaminases levels
- Complete atrioventricular heart block in congenital hypothyroidism
- Pro - inflammatory cytokines, lymphocyte subsets and intravenous immunoglobulin therapy in guillain - barre syndrome
- Peroneal nerve injuries as a complication of injection
- Hydatid cyst mimicking pulmonary hematoma in a patient with hemophilia a
- Magnetic resonance imaging ( MR ) findings in isolated growth hormone deficiency
- Plaque radiotherapy in the management of retinoblastoma
- Cherubism: A radiological and clinical presentation
- Salmonella gastroenteritis in children
- Evaluation of renal functions in children with congenital heart disease before and after cardiac angiography
- Bilateral proptosis caused by orbital myositis ( A case report )
- Balloon dilation of stenotic nonvalved conduits after fontan operation
- Isovaleric acidemia ( clinical presentation of 6 cases )
- Plasma thrombomodulin levels in early respiratory distress syndrome
- Latex sensitivity among hospital employees and atopic children
- Recurrent meningitis associated with congenital paravertebral dermal sinus tract
- Myelodysplastic syndrome in a child with a history of medulloblastoma
- The effects of L - carnitine on respiratory function tests in children undergoing chronic hemodialysis
- A comparison of different filters for white cell reduction
- Diploid - triploid and tetraploid mosaicism in a child with cryptogenic cirrhosis and membranous glomerulonephritis: A causal relationship or coincidental association?
- In utero defecation: A new concept
- Congenital epulis of the newborn ( A case report )
- The results of long - term growth hormone replacement therapy in Turkish children with growth hormone deficiency
- Autosomal recessive polycystic kidney disease: Mapping to chromosomal region of 6p21 - CEN in a turkish child
- Citrullinemia ( Clinical experience with 23 cases )
- İntraventricular hemorrhage in preterm newborns
- Serum malondialdehyde concentration as a measure of oxygen free radical damage in preterm infants
- Scurvy ( A case report )
- An acute vasculitis resembling polyarteritis nodosa
- Fatal outcome of infantile oxalosis: Case reports from three families and a review of literature
- Bruce treadmill test in healthy turkish children: Endurance time, heart rate, blood pressure and electrocardiographic changes
- Blockade of acute grade IV skin and eye graft - versus - host disease by anti - interleukin -2 receptor monoclonal antibody in genoidentical bone marrow transplantation setting
- A sex - specific difference in homozygosity for HLA - DR53 in newborns
- Kearns - sayre syndrome ( A case report )
- Demographic features and psychosocial problems in single - parent families: 1985 to 1995
- Left ventricular diastolic abnormalities in children with Beta - Thalassemia major: A doopler echocardiographic study
- Persistent diffuse peritonitis in children
- Congenital cystic adenomatoid malformation ( Report of two cases and review of the literature )
- Two siblings with fetal hydantoin syndrome
- A diffuse form of neurofibroma of bladder in a child with von recklinghausen disease
- Subcutaneous granuloma annulare and IgA-IgG2 deficiency
- Use of localized proton nuclear magnetic resonance spectroscopy in canavan' s disease
- Extrapontine myelinolysis in a nine-year-old child
- A multicenter child maltreatment study: Twenty-eight cases followed-up on a multidisciplinary basis
- Noninvasive cardiac evaluation of young patient with cystic fibrosis
- Recombinant interferon-alfa-2A with or without steroid pretreatment in children with chronic hepatitis B
- Early assessment of pulmonary involvement in limited scleroderma ( A case report )
- Rh blood group system in Turkey
- A family presenting goltz syndrome ( Focal dermal hypoplasia ) in three generations
- Attention deficit hyperactivity disorder ( ADHD ): A practical scale for pediatricians
- A case of truncus arteriosus type II
- Alpha-2-macroglobulin levels in early respiratory distress syndrome
- Acute rheumatic fever with threee major criteria: Polyarthritis, carditis and chorea (A case report)
- Toxic methemoglobinemia after injection of prilocaine in a newborn ( A case report )
- The clinical predictors of intrauterine fetal death
- Herpes encephalitis in children ( MRI assessment )
- Turkish experience with rhabdomyosarcoma: An analysis of 255 patients for 20 years
- Fc$gamma$ receptor allotypes in children with bacterial meningitis ( A preliminary study )
- ISSN: 0041-4301
- Yayın Aralığı: Yılda 6 Sayı
- Başlangıç: 1958
- Yayıncı: Hacettepe Üniversitesi Çocuk Sağlığı Enstitüsü Müdürlüğü
49.3b 16b