journal of pediatric neurology سال:2010 - دوره:8

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journal of pediatric neurology
سال:2010 - دوره:8 - شماره:2

ARX and SHH gene mutation analyses revealed no mutation in patients with agenesis/dysgenesis of the corpus callosum - صفحه:157-162 Biochemical parameters predictive of neuronal damage in children with neonatal hypoxic ischemia - صفحه:135-149 Carbonic anhydrase II deficiency syndrome: A report of 18 new Saudi Arabian cases - صفحه:163-174 Caudal regression syndrome with vestigial tail and esophageal duplication cyst - صفحه:237-240 Cognitive function and event related potentials in children with beta-thalassemia - صفحه:187-192 Deep cerebral venous thrombosis: Rare cause of stroke in children - صفحه:215-218 Depersonalization disorder in pre-adolescent child of acute disseminated encephalomyelitis - صفحه:211-214 Failure of diffusion weighted MRI to detect severe hypoxic-ischemic encephalopathy in a child - صفحه:231-235 Hallervorden spatz disease: A case report - صفحه:219-222 Hemimegalencephaly with microgyric - Agyric cortex - صفحه:241-242 Inverted duplication of chromosome 15 (dic15q11) diagnosed by FISH in a patient with neurological problems - صفحه:205-209 Joubert syndrome and related disorders: Report of five Tunisian cases - صفحه:199-204 Polymorphisms of the ABCA1 and PON1 genes in determining the predisposition to ischemic stroke in children - صفحه:151-156 Polyunsaturated fatty acids in children with idiopathic intractable epilepsy: Serum levels and therapeutic response - صفحه:175-185 Ptosis as unusual presentation of a cerebral arteriovenous malformation - صفحه:227-229 Rasmussen's encephalitis: A case report - صفحه:223-226 The Churg-Strauss syndrome - صفحه:131-133 Tissue plasminogen activator in children with idiopathic and intractable epilepsies - صفحه:193-197