Volume 60 Issue 1 (2018)

Published: February 28, 2018

Original Articles

Clinical and molecular evaluation of 16 patients with Rett syndrome
The value of nasopharyngeal aspirate, gastric aspirate and bronchoalveolar lavage fluid in the diagnosis of childhood tuberculosis
C1q nephropathy among children with nephrotic syndrome: Ten-year experience from a pediatric nephrology unit
Investigation of the frequency of iron insufficiency among infants in a population in which routine iron supplementation is implemented
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
Knowledge levels related to allergen specific immunotherapy and perspectives of parents whose children were diagnosed with asthma and/or allergic rhinitis in Turkey
Outbreak of varicella in preschool children despite one-dose vaccination
Assessment of central venous catheterization and complications in a tertiary pediatric intensive care unit
Restless leg syndrome in children with celiac disease

Case Reports

A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings
Hemolytic uremic syndrome and IgA nephropathy in a child: Coincidence or not?
A rare reason in a child with feeding intolerance: Intravaginal struvite stone
Anauxetic dysplasia: A rare clinical entity
Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region
Acute peripheral facial paralysis following varicella infection: An uncommon complication
Pediatric primary anaplastic ganglioglioma with malignant neuronal component
Multiple cranial nerve schwannomas and meningiomas as a hallmark sign of neurofibromatosis type 2 in a child
Phenytoin induced dystonia
Transcatheter retrieval of embolized catheter using venovenous loop in a neonate