The Turkish Journal of Pediatrics 2018 , Vol 60 , Num 1
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.

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.

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