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Epilepsy Research|January 9, 2021
Contribution of rare genetic variants to drug response in absence epilepsyKenneth A Myers, Mark F Bennett, Bronwyn E Grinton, et al.BMJ Open|September 28, 2019
Understanding autism spectrum disorder and social functioning in children with neurofibromatosis type 1: protocol for a cross-sectional multimodal studyKristina M Haebich, Natalie A Pride, Karin S Walsh, et al.Journal of Autism and Developmental Disorders|April 21, 2022
Sex- and age-related differences in autistic behaviours in children with neurofibromatosis type 1Anita K Chisholm, Francesca Lami, Kristina M Haebich, et al.Molecular Autism|July 2, 2026
Autism in neurofibromatosis type 1: prevalence, phenotype and clinical implicationsJonathan M Payne, Kristina M Haebich, Anita K Chisholm, et al.Molecular Psychiatry|September 18, 2022
Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain developmentAntony Kaspi, Michael S Hildebrand, Victoria E Jackson, et al.Epilepsia|January 21, 2021
The severe epilepsy syndromes of infancy: A population-based studyKatherine B Howell, Jeremy L Freeman, Mark T Mackay, et al.Neurology|July 22, 2025
Development and Adaptive Function in Individuals With SCN2A-Related DisordersBeatrice Southby Goad, Jill Rodda, Meagan Allen, et al.Pageof 3