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The Turkish Journal of Pediatrics 2018 , Vol 60 , Num 3
Original Article
GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author Efficacy of rufinamide in childhood refractory epilepsy Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author Glycemic control and health behaviors in adolescents with type 1 diabetes Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author The influence of media on the sleep quality in adolescents Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author Hereditary spherocytosis: Retrospective evaluation of 65 children Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author Advantage of the subcutaneous immunoglobulin replacement therapy in primary immunodeficient patients with or without secondary protein loss Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author High alert medications administration errors in neonatal intensive care unit: A pediatric tertiary hospital experience Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author Gelsolin levels in patients with bronchiolitis Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author Attitudes of physicians concerning vaccines not included in the national immunization schedule Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author Birth outcomes after inadvertent use of category X drugs contraindicated in pregnancy: Where is the real risk? Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author
Case Report
Neonatal atrial flutter: Three cases and review of the literature Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author A case of steroid-resistance Hashimoto's encephalopathy presenting with sensorimotor polyneuropathy Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author A novel mutation of the MYH7 gene in a patient with hypertrophic cardiomyopathy Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author A case of atypically located leiomyoma mimicking axillary lymphadenomegaly Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author A case of myeloid sarcoma presenting with an orbital mass, hearing loss, and multiple cranial neuropathies Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author Polyarteritis nodosa in case of familial Mediterranean fever Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author An infant case of renovascular hypertension in moyamoya disease treated by angioplasty Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author Chelation therapy for secondary neonatal iron over load: Lessons learned from rhesus hemolytic disease Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author Granulomatous amebic encephalitis caused by Acanthamoeba in an immuncompetent child Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author Arthropathy-like findings and a carpal tunnel syndrome as the presenting features of Scheie syndrome: Three cases from the same family Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author
Short Report
Arrhythmia in thiamine responsive megaloblastic anemia syndrome Turkish Abstract Abstract Full Text:PDF Similar Articles Mail to Author
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