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Developmental Medicine and Child Neurology|June 25, 2013
An investigation into the relationship between vigabatrin, movement disorders, and brain magnetic resonance imaging abnormalities in children with infantile spasmsChoong Yi Fong, John P Osborne, Stuart W Edwards, et al.Neurology(R) Neuroimmunology & Neuroinflammation|October 11, 2024
Pediatric MOG-Ab-Associated Encephalitis: Supporting Early Recognition and TreatmentNee Na Kim, Dimitrios Champsas, Michael Eyre, et al.Neurology|June 13, 2024
Validation of the 2023 International Diagnostic Criteria for MOGAD in a Selected Cohort of Adults and ChildrenJames A Varley, Dimitrios Champsas, Timothy Prossor, 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.Plos One|November 16, 2017
Childhood tuberculosis is associated with decreased abundance of T cell gene transcripts and impaired T cell functionCheryl Hemingway, Maurice Berk, Suzanne T Anderson, et al.The Lancet. Neurology|January 27, 2023
Diagnosis of myelin oligodendrocyte glycoprotein antibody-associated disease: International MOGAD Panel proposed criteriaBrenda Banwell, Jeffrey L Bennett, Romain Marignier, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 18, 2024
Long term outcome in non-multiple sclerosis paediatric acquired demyelinating syndromesEvangeline Wassmer, Charly Billaud, Michael Absoud, et al.Neurology|January 9, 2026
Investigating the Frequency and Outcome of Central Vein Sign and Paramagnetic Rim Lesions in Children With MOGADRiccardo Nistri, Laura Cacciaguerra, Simone Sacco, et al.Nature Communications|April 8, 2025
Enabling new insights from old scans by repurposing clinical MRI archives for multiple sclerosis researchPhilipp Goebl, Jed Wingrove, Omar Abdelmannan, et al.Brain : a Journal of Neurology|June 18, 2010
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)Philippa B Mills, Emma J Footitt, Kevin A Mills, et al.Pageof 9