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Developmental Medicine and Child Neurology|January 20, 2019
Utility and safety of plasma exchange in paediatric neuroimmune disordersMichael Eyre, Yael Hacohen, Kate Lamb, et al.Brain : a Journal of Neurology|July 27, 2012
A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutationsPinki Munot, Dawn E Saunders, Dianna M Milewicz, et al.Developmental Medicine and Child Neurology|November 21, 2012
The clinical utility of an SCN1A genetic diagnosis in infantile-onset epilepsyAndreas Brunklaus, Liam Dorris, Rachael Ellis, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 24, 2012
Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigensYael Hacohen, Sukhvir Wright, Patrick Waters, et al.Seizure|January 29, 2016
Effectiveness of antiepileptic therapy in patients with PCDH19 mutationsJan Lotte, Thomas Bast, Peter Borusiak, et al.Pageof 2