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Epilepsia Open|September 18, 2025
Current practices and trends in surgical decision-making for children with Lennox-Gastaut syndrome: A cross-sectional survey by the Pediatric Epilepsy Research ConsortiumMichelle Y Chiu, Cynthia G Keator, Aaron E L Warren, et al.Nature Communications|May 5, 2026
Global mitochondrial connectivity map reveals the landscape of yeast functional assemblies and conserved protein communitiesMatthew Jessulat, Sadhna Phanse, Hiroyuki Aoki, et al.Nature|February 6, 2009
Association of reactive oxygen species levels and radioresistance in cancer stem cellsMaximilian Diehn, Robert W Cho, Neethan A Lobo, et al.Brain : a Journal of Neurology|February 5, 2013
K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivityNancy Mokbel, Biljana Ilkovski, Michaela Kreissl, et al.Epilepsia|December 28, 2020
Design and implementation of electronic health record common data elements for pediatric epilepsy: Foundations for a learning health care systemZachary M Grinspan, Anup D Patel, Renée A Shellhaas, et al.Annals of Neurology|April 14, 2016
Mutation-specific effects on thin filament length in thin filament myopathyJosine M de Winter, Barbara Joureau, Eun-Jeong Lee, et al.American Journal of Human Genetics|May 14, 2013
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegiaEmily C Oates, Alexander M Rossor, Majid Hafezparast, et al.Orphanet Journal of Rare Diseases|November 19, 2015
Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birthEmily J Todd, Kyle S Yau, Royston Ong, et al.Science (New York, N.Y.)|November 20, 2020
Fire and biodiversity in the AnthropoceneLuke T Kelly, Katherine M Giljohann, Andrea Duane, et al.Brain : a Journal of Neurology|December 16, 2014
Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2Alexander M Rossor, Emily C Oates, Hannah K Salter, et al.Pageof 83