how to cite this article: ghofrani m. approach to the first unprovoked seizure- part ii. iran j child neurol. 2013 autumn; 7(4):1-5. abstract the approach to a child who has experienced a first unprovoked generalized tonic-clonic seizure is challenging and at the same time controversial. how to establish the diagnosis, ways and means of investigation and whether treatment is appropriate, are di...

background and objective: injuries have been identified as one of the most important causes of disability and death in humans, and children are more vulnerable to injuries than adults because of limitations in the detection of risk. the present study aimed to investigate the children aged 1 to 59 months death due to injuries cases in the area covered by the shahid beheshti university of medical...

how to cite this article: tavasoli ar, gharib b, alizadeh h, farshadmoghaddam h, memarian s, ashrafi mr, sharifzade m. brain on fires: super refractory seizure in a 7 year old boy. iran j child neurol. autumn 2016; 10(4):80-85. abstract we present a 7 year old boy afflicted with super-refractory seizure that responded poorly to antiepileptic drugs and sustained a long course of hospitalization ...

how to cite this article: ghofrani m. approach to the first unprovoked seizure- part i. iran j child neurol. 2013 summer; 7(3): 1- 5.   the approach to a child who has experienced a first unprovoked generalized tonic-clonic seizure is challenging and at the same time controversial. how to establish the diagnosis, ways and means of investigation and whether treatment is appropriate, are differen...

Motulsky, A. G., and Kampbell-Kraut, J. M. (1961). Population genetics of glucose-6-phosphate-dehydrogenase deficiency of the red cells. Proceedings of Conference on Genetics in Disease, p. 159. Grune and Stratton, New York and London. Shahidi, N. T., and Diamond, L. K. (1959). Enzyme deficiency in erythrocytes in congenital nonspherocytic hemolytic anemia. Pediatrics, 24, 245. Taj-Eldin, S., A...

how to cite this article: heidari mm , khatami m, pourakrami j. novel point mutations in frataxin gene in iranian patients with friedreich’s ataxia. iran j child neurol. 2014 winter; 8(1):32-36.   objective friedreich’s ataxia is the most common form of hereditary ataxia with autosomal recessive pattern. more than 96% of patients are homozygous for gaa repeat extension on both alleles in the fi...

Andersen, D. H., and Kelly, J. (1956). Endocardial fibro-elastosis: I. endocardial fibro-elastosis associated with congenital malformations of the heart. Pediatrics, 18, 513, Dordick, J. R. (1951). Diffuse endocardial fibrosis and cardiac hypertrophy in infancy: report of two cases in consecutive siblings. American Journal of Clinical Pathology, 21, 743. Forfar, J. O., Miller, R. A., Bain, A. D...