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Developmental Medicine and Child Neurology|June 14, 2022
Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practiceIngrid E Scheffer, Caitlin A Bennett, Deepak Gill, et al.Epilepsia|March 19, 2009
Neuropsychological and functional MRI studies provide converging evidence of anterior language dysfunction in BECTSLeasha M Lillywhite, Michael M Saling, A Simon Harvey, et al.Epilepsy Research|August 5, 2017
The effect of the ketogenic diet on the developing skeletonPeter J Simm, Jillian Bicknell-Royle, Jock Lawrie, et al.Brain : a Journal of Neurology|April 3, 2018
The ventrolateral medulla and medullary raphe in sudden unexpected death in epilepsySmriti Patodia, Alyma Somani, Megan O'Hare, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 5, 2019
Nomenclature of Genetically Determined Myoclonus Syndromes: Recommendations of the International Parkinson and Movement Disorder Society Task ForceSterre van der Veen, Rodi Zutt, Christine Klein, et al.Neurology|September 25, 2023
Movement Disorders in Patients With Genetic Developmental and Epileptic EncephalopathiesSterre van der Veen, Gabrielle T W Tse, Alessandro Ferretti, et al.IEEE Transactions on Bio-Medical Engineering|January 25, 2018
Consistency of Long-Term Subdural Electrocorticography in HumansEwan S Nurse, Sam E John, Dean R Freestone, et al.Human Molecular Genetics|February 25, 2006
SRPX2 mutations in disorders of language cortex and cognitionPatrice Roll, Gabrielle Rudolf, Sandrine Pereira, et al.Developmental Medicine and Child Neurology|April 28, 2015
Favourable response to ketogenic dietary therapies: undiagnosed glucose 1 transporter deficiency syndrome is only one factorNatasha E Schoeler, Judith Helen Cross, Suzanne Drury, et al.Neurology|August 15, 2002
X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARXIngrid E Scheffer, R H Wallace, F L Phillips, et al.Pageof 74