Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Seizure|August 14, 2012
Prevalence of active epilepsy in rural Tanzania: a large community-based survey in an adult populationEwan Hunter, Jane Rogathi, Simukai Chigudu, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|October 7, 2016
Slow wave sleep and accelerated forgettingKathryn E Atherton, Anna C Nobre, Alpar S Lazar, et al.
Neuropathology and Applied Neurobiology|March 20, 2015
Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial diseaseNichola Z Lax, John Grady, Alex Laude, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 11, 2024
Neurophysiological and imaging biomarkers of lower motor neuron dysfunction in motor neuron diseases/amyotrophic lateral sclerosis: IFCN handbook chapterCindy Shin-Yi Lin, James Howells, Seward Rutkove, et al.
Seizure|December 2, 2011
Co-morbidity of epilepsy in Tanzanian children: a community-based case-control studyKathryn Burton, Jane Rogathe, Roger G Whittaker, et al.
Brain : a Journal of Neurology|December 23, 2011
Sensory neuronopathy in patients harbouring recessive polymerase γ mutationsNichola Z Lax, Roger G Whittaker, Philippa D Hepplewhite, et al.
NMR in Biomedicine|April 9, 2025
Measurement of Twitch Dynamics in Response to Exercise Induced Changes in Mitochondrial Disease Using Motor Unit Magnetic Resonance Imaging (MUMRI): A Proof-of-Concept StudyMatthew G Birkbeck, Mathew Elameer, Linda Heskamp, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2009
A nonsynaptic mechanism underlying interictal discharges in human epileptic neocortexAnita K Roopun, Jennifer D Simonotto, Michelle L Pierce, et al.
Annals of Neurology|September 19, 2015
Epilepsy in adults with mitochondrial disease: A cohort studyRoger G Whittaker, Helen E Devine, Grainne S Gorman, et al.
Plos One|September 28, 2017
Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndromeMallory C Shields, Matthew R Bowers, McKenzie M Fulcer, et al.
Pageof 5