Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|March 22, 2014
Do the clinical features in infantile-onset saccade initiation delay (congenital ocular motor apraxia) correlate with brain magnetic resonance imaging findings?Michael S Salman, Kristin M Ikeda
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 10, 2010
Disconnections in infantile-onset saccade initiation delay: a hypothesisMichael S Salman, Kristin M Ikeda
Epilepsy & Behavior Case Reports|April 6, 2017
Evolution of epilepsy in hemimegalencephaly from infancy to adulthood: Case report and review of the literatureKristin M Ikeda, Seyed M Mirsattari
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 20, 2013
The syndrome of infantile-onset saccade initiation delayMichael S Salman, Kristin M Ikeda
Brain Topography|October 14, 2024
Validation of On-Head OPM MEG for Language Laterality AssessmentLindsey Power, Timothy Bardouille, Kristin M Ikeda, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 3, 2026
Exploring the efficacy and safety of perampanel in epilepsia partialis continua: A case seriesSetareh Lahsaee, Kristin M Ikeda, Stephanie Woodroffe, et al.
International Journal of MS Care|October 17, 2015
Plasma Exchange in a Patient with Tumefactive, Corticosteroid-Resistant Multiple SclerosisKristin M Ikeda, Donald H Lee, J Alexander Fraser, et al.
British Journal of Haematology|June 23, 2025
Lamotrigine and anti-seizure medications in HLH: A systematic reviewYaswanta K Gummadi, Ashley E Sutherland, Kristin M Ikeda, et al.
Neurocritical Care|December 29, 2016
Isoflurane Use in the Treatment of Super-Refractory Status Epilepticus is Associated with Hippocampal Changes on MRIKristin M Ikeda, Robert Connors, Donald H Lee, et al.
Molecular Syndromology|June 28, 2021
Potential Pitfalls in Pre-implantation Genetic Diagnosis in a Patient with Tuberous Sclerosis and Isolated Mosaicism for a <i>TSC2</i> Variant in Renal TissueKristin M Ikeda, Andrew A House, Dervla M Connaughton, et al.
Pageof 2