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Neuropediatrics|August 12, 2003
An unusual case of benign reflex myoclonic epilepsy of infancyM A Kurian, M D KingEuropean Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 1, 2018
Review of the phenotype of early-onset generalised progressive dystonia due to mutations in KMT2BK M Gorman, E Meyer, M A KurianPaediatric Drugs|July 12, 2014
Clinical features and pharmacotherapy of childhood monoamine neurotransmitter disordersJ Ng, S J R Heales, M A KurianAdvances and Technical Standards in Neurosurgery|August 17, 2022
Convection-Enhanced Delivery in Children: Techniques and ApplicationsK Aquilina, A Chakrapani, L Carr, et al.Journal of Neurology|February 22, 2025
Genetic therapies for movement disorders - current statusJ Sartorelli, J Ng, A A Rahim, et al.AJNR. American Journal of Neuroradiology|November 3, 2022
Expanding the Spectrum of Early Neuroradiologic Findings in β Propeller Protein-Associated NeurodegenerationA Papandreou, A K S Soo, R Spaull, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 17, 2004
Neonatal seizures and limb malformations associated with liver-specific complex IV respiratory chain deficiencyM A Kurian, E S O'Mahoney, P Rustin, et al.Journal of Inherited Metabolic Disease|April 7, 2004
Straight-chain acyl-CoA oxidase deficiency presenting with dysmorphia, neurodevelopmental autistic-type regression and a selective pattern of leukodystrophyM A Kurian, S Ryan, G T N Besley, et al.Neuroscience and Biobehavioral Reviews|May 22, 2017
A review of psychiatric co-morbidity described in genetic and immune mediated movement disordersK J Peall, M S Lorentzos, I Heyman, et al.Neuropediatrics|November 10, 2004
Short-chain acyl-CoA dehydrogenase deficiency associated with early onset severe axonal neuropathyM A Kurian, L Hartley, Z Zolkipli, et al.Pageof 2