The Turkish Journal of Pediatrics 2018 , Vol 60 , Num 3
GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria.

Efficacy of rufinamide in childhood refractory epilepsy.

Glycemic control and health behaviors in adolescents with type 1 diabetes.

The influence of media on the sleep quality in adolescents.

Hereditary spherocytosis: Retrospective evaluation of 65 children.

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.

Birth outcomes after inadvertent use of category X drugs contraindicated in pregnancy: Where is the real risk?.

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 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.

Chelation therapy for secondary neonatal iron over load: Lessons learned from rhesus hemolytic disease.

Granulomatous amebic encephalitis caused by Acanthamoeba in an immuncompetent child.

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.

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