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Richard J Leventer

Showing results (41-50 of 146) with videos related to

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JIMD Reports|February 3, 2026
Metabolic Stroke: Atypical Presentation of Succinic Semialdehyde Dehydrogenase DeficiencySharmila Kiss, Richard J Leventer, Cormac Duff, et al.
Annals of Clinical and Translational Neurology|January 12, 2021
Gradient of brain mosaic RHEB variants causes a continuum of cortical dysplasiaWei Shern Lee, Sara Baldassari, Mathilde Chipaux, et al.
Epilepsia|December 17, 2022
Intrinsic and secondary epileptogenicity in focal cortical dysplasia type IIEmma Macdonald-Laurs, Aaron E L Warren, Wei Shern Lee, et al.
Brain Communications|February 19, 2021
Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencingChloe A Stutterd, Stefanie Brock, Katrien Stouffs, et al.
Cerebral Cortex (New York, N.Y. : 1991)|October 27, 2020
Structural Neuroplastic Responses Preserve Functional Connectivity and Neurobehavioural Outcomes in Children Born Without Corpus CallosumVanessa Siffredi, Maria G Preti, Valeria Kebets, et al.
Neurology. Genetics|October 30, 2016
Heterozygous mutations in <i>HSD17B4</i> cause juvenile peroxisomal D-bifunctional protein deficiencyDavid J Amor, Ashley P L Marsh, Elsdon Storey, et al.
Neuroimage. Clinical|June 15, 2021
Intra- and inter-hemispheric structural connectome in agenesis of the corpus callosumMinghui Shi, Lorena G A Freitas, Megan M Spencer-Smith, et al.
Neurology. Genetics|March 18, 2024
Ectopic HCN4 Provides a Target Biomarker for the Genetic Spectrum of mTORopathiesMatthew Coleman, Paulo Pinares-Garcia, Sarah E Stephenson, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 26, 2021
Clinical seizure manifestations in the absence of synaptic connectionsEmma Macdonald-Laurs, Catherine A Bailey, Sarah Barton, et al.
Annals of Clinical and Translational Neurology|January 4, 2018
Neuropathology of childhood-onset basal ganglia degeneration caused by mutation of <i>VAC14</i>Chloe Stutterd, Peter Diakumis, Melanie Bahlo, et al.
Pageof 15

Showing results (41-50 of 146) with videos related to

Sort By:
Pageof 15
JIMD Reports|February 3, 2026
Metabolic Stroke: Atypical Presentation of Succinic Semialdehyde Dehydrogenase DeficiencySharmila Kiss, Richard J Leventer, Cormac Duff, et al.
Annals of Clinical and Translational Neurology|January 12, 2021
Gradient of brain mosaic RHEB variants causes a continuum of cortical dysplasiaWei Shern Lee, Sara Baldassari, Mathilde Chipaux, et al.
Epilepsia|December 17, 2022
Intrinsic and secondary epileptogenicity in focal cortical dysplasia type IIEmma Macdonald-Laurs, Aaron E L Warren, Wei Shern Lee, et al.
Brain Communications|February 19, 2021
Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencingChloe A Stutterd, Stefanie Brock, Katrien Stouffs, et al.
Cerebral Cortex (New York, N.Y. : 1991)|October 27, 2020
Structural Neuroplastic Responses Preserve Functional Connectivity and Neurobehavioural Outcomes in Children Born Without Corpus CallosumVanessa Siffredi, Maria G Preti, Valeria Kebets, et al.
Neurology. Genetics|October 30, 2016
Heterozygous mutations in <i>HSD17B4</i> cause juvenile peroxisomal D-bifunctional protein deficiencyDavid J Amor, Ashley P L Marsh, Elsdon Storey, et al.
Neuroimage. Clinical|June 15, 2021
Intra- and inter-hemispheric structural connectome in agenesis of the corpus callosumMinghui Shi, Lorena G A Freitas, Megan M Spencer-Smith, et al.
Neurology. Genetics|March 18, 2024
Ectopic HCN4 Provides a Target Biomarker for the Genetic Spectrum of mTORopathiesMatthew Coleman, Paulo Pinares-Garcia, Sarah E Stephenson, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 26, 2021
Clinical seizure manifestations in the absence of synaptic connectionsEmma Macdonald-Laurs, Catherine A Bailey, Sarah Barton, et al.
Annals of Clinical and Translational Neurology|January 4, 2018
Neuropathology of childhood-onset basal ganglia degeneration caused by mutation of <i>VAC14</i>Chloe Stutterd, Peter Diakumis, Melanie Bahlo, et al.
Pageof 15