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Orrin Devinsky

Showing results (631-640 of 674) with videos related to

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Ebiomedicine|July 3, 2022
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanismFrancesco Miceli, Charissa Millevert, Maria Virginia Soldovieri, et al.
Lancet (London, England)|September 20, 2025
Risk markers for sudden unexpected death in epilepsy: an observational, prospective, multicentre cohort studyManuela Ochoa-Urrea, Xi Luo, Laura Vilella, et al.
Scientific Data|June 27, 2019
iEEG-BIDS, extending the Brain Imaging Data Structure specification to human intracranial electrophysiologyChristopher Holdgraf, Stefan Appelhoff, Stephan Bickel, et al.
Epilepsia|August 5, 2025
Evidence demands action: An invitation to share the burden of proofDanielle M Andrade, Anne T Berg, Arunan Selvarajah, et al.
Nature Neuroscience|August 9, 2022
Publisher Correction: Viral manipulation of functionally distinct interneurons in mice, non-human primates and humansDouglas Vormstein-Schneider, Jessica D Lin, Kenneth A Pelkey, et al.
Epilepsia|March 4, 2025
Dravet syndrome: From neurodevelopmental to neurodegenerative disease?Arunan Selvarajah, Andrea Sabo, Carolina Gorodetsky, et al.
Journal of Medical Genetics|January 26, 2017
<i>STAG1</i> mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disabilityDaphné Lehalle, Anne-Laure Mosca-Boidron, Amber Begtrup, et al.
Nature Neuroscience|August 19, 2020
Viral manipulation of functionally distinct interneurons in mice, non-human primates and humansDouglas Vormstein-Schneider, Jessica D Lin, Kenneth A Pelkey, et al.
Journal of Medical Genetics|July 1, 2016
De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsyIris M de Lange, Katherine L Helbig, Sarah Weckhuysen, et al.
Genes|August 29, 2024
A Genotype/Phenotype Study of <i>KDM5B</i>-Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense VariantsMaria Carla Borroto, Coralie Michaud, Chloé Hudon, et al.
Pageof 68

Showing results (631-640 of 674) with videos related to

Sort By:
Pageof 68
Ebiomedicine|July 3, 2022
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanismFrancesco Miceli, Charissa Millevert, Maria Virginia Soldovieri, et al.
Lancet (London, England)|September 20, 2025
Risk markers for sudden unexpected death in epilepsy: an observational, prospective, multicentre cohort studyManuela Ochoa-Urrea, Xi Luo, Laura Vilella, et al.
Scientific Data|June 27, 2019
iEEG-BIDS, extending the Brain Imaging Data Structure specification to human intracranial electrophysiologyChristopher Holdgraf, Stefan Appelhoff, Stephan Bickel, et al.
Epilepsia|August 5, 2025
Evidence demands action: An invitation to share the burden of proofDanielle M Andrade, Anne T Berg, Arunan Selvarajah, et al.
Nature Neuroscience|August 9, 2022
Publisher Correction: Viral manipulation of functionally distinct interneurons in mice, non-human primates and humansDouglas Vormstein-Schneider, Jessica D Lin, Kenneth A Pelkey, et al.
Epilepsia|March 4, 2025
Dravet syndrome: From neurodevelopmental to neurodegenerative disease?Arunan Selvarajah, Andrea Sabo, Carolina Gorodetsky, et al.
Journal of Medical Genetics|January 26, 2017
<i>STAG1</i> mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disabilityDaphné Lehalle, Anne-Laure Mosca-Boidron, Amber Begtrup, et al.
Nature Neuroscience|August 19, 2020
Viral manipulation of functionally distinct interneurons in mice, non-human primates and humansDouglas Vormstein-Schneider, Jessica D Lin, Kenneth A Pelkey, et al.
Journal of Medical Genetics|July 1, 2016
De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsyIris M de Lange, Katherine L Helbig, Sarah Weckhuysen, et al.
Genes|August 29, 2024
A Genotype/Phenotype Study of <i>KDM5B</i>-Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense VariantsMaria Carla Borroto, Coralie Michaud, Chloé Hudon, et al.
Pageof 68