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Neurology. Genetics|November 23, 2016
De novo FGF12 mutation in 2 patients with neonatal-onset epilepsyIlaria Guella, Linda Huh, Marna B McKenzie, et al.American Journal of Human Genetics|August 5, 2017
De Novo Mutations in YWHAG Cause Early-Onset EpilepsyIlaria Guella, Marna B McKenzie, Daniel M Evans, et al.American Journal of Human Genetics|July 4, 2017
Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic EncephalopathyAnna Lehman, Samrat Thouta, Grazia M S Mancini, et al.Pediatrics|June 3, 2015
Recovery From Central Nervous System Acute Demyelination in ChildrenJulia O'Mahony, Ruth Ann Marrie, Audrey Laporte, et al.Intensive Care Medicine|October 26, 2020
Neuromuscular blockade in patients with ARDS: a rapid practice guidelineWaleed Alhazzani, E Belley-Cote, M H Møller, et al.The Journal of Clinical Investigation|April 10, 2018
Humanized mouse model of Rasmussen's encephalitis supports the immune-mediated hypothesisHania Kebir, Lionel Carmant, François Fontaine, et al.Neurosurgery|June 30, 2015
Resective Epilepsy Surgery for Tuberous Sclerosis in Children: Determining Predictors of Seizure Outcomes in a Multicenter Retrospective Cohort StudyAria Fallah, Shaun D Rodgers, Alexander G Weil, et al.Malaria Journal|May 25, 2022
Recommendations for environmental risk assessment of gene drive applications for malaria vector controlJohn B Connolly, John D Mumford, Debora C M Glandorf, et al.Frontiers in Neurology|June 6, 2019
Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset EpilepsyMichelle Demos, Ilaria Guella, Conrado DeGuzman, et al.Neurology|January 21, 2009
Incidence of acquired demyelination of the CNS in Canadian childrenB Banwell, J Kennedy, D Sadovnick, et al.Pageof 29