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Abstracts of the 39th Annual Meeting of the Society of Neuropediatrics
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Oexle, K
Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature
Oh, J
Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4
Ohlenbusch, A
Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders
Ohlmann, JAK
Panic attacks in girls with double cortex syndrome: ictal amaurosis
Olbert, C
Diagnostics and management of pediatric headaches at a University Hospital
Olze, A
Panic attacks in girls with double cortex syndrome: ictal amaurosis
Omran, H
Rare cause of oculomotor palsy
Vitamin B in paediatric neurology
Ketogenic diet in children with pharmacoresistant epilepsy
Opladen, T
Neurometabolic changes in patients with subacute sclerosing panencephalitis
Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene
Tetrahydrobiopterin deficiencies: an international survey of clinical and biochemical features, treatment strategies and follow-up of 626 patients
Otzelberger, B
Quality of life and mental health of neuropediatric patients