journal of pediatric neurology سال:2012 - دوره:10

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journal of pediatric neurology
سال:2012 - دوره:10 - شماره:1

A case of congenital muscular dystrophy similar to fukuyama-type with a missense mutation in the fukutin gene - صفحه:63-66 A case of galactosialidosis with renal failure and hippocampal sclerosis - صفحه:45-48 A case of isolated oculomotor nerve palsy in a girl - صفحه:49-51 Isolated sulfite oxidase deficiency,a rare neurodegenerative disorder which mimics hypoxic-ischemic encephalopathy - صفحه:67-71 Linear scleroderma en coup de sabre - صفحه:73-74 Novel cytochrome B gene mutations causing mitochondrial disease in autism - صفحه:35-40 Post-pump chorea: Choreoathetosis after cardiac surgery with hypothermia and extracorporeal circulation - صفحه:57-61 Primary amenorrhea in a 17-year-old patient with chronic hydrocephalus from an ependymoma - صفحه:41-44 Retinal astrocytic hamartomas in tuberous sclerosis complex - صفحه:75-76 Sturge-Weber syndrome: A rare entity - صفحه:77-78 The prevalence,burden and cognizance of migraine in adolescent girls - صفحه:29-34 Trans-cranial Doppler in prediction of adverse outcome in asphyxiated neonates - صفحه:7-14 Transmission disequilibrium test and haplotype analysis of the MCP-1 -2518G/A polymorphism with Tourette syndrome in Chinese Han trios - صفحه:1-5 Understanding autism in Saudi Arabia: A qualitative analysis of the community and cultural context - صفحه:15-22 Vagus nerve stimulator-induced apneas and hypopneas in a child with refractory seizures - صفحه:53-56