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Ebiomedicine
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July 3, 2022
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism
Francesco 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 study
Manuela 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 electrophysiology
Christopher Holdgraf, Stefan Appelhoff, Stephan Bickel, et al.
Epilepsia
|
August 5, 2025
Evidence demands action: An invitation to share the burden of proof
Danielle 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 humans
Douglas 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 disability
Daphné 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 humans
Douglas 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 epilepsy
Iris 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 Variants
Maria Carla Borroto, Coralie Michaud, Chloé Hudon, et al.
Page
of 68
Search research articles
Search
Showing results (631-640 of 674) with videos related to
Sort By:
Page
of 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 mechanism
Francesco 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 study
Manuela 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 electrophysiology
Christopher Holdgraf, Stefan Appelhoff, Stephan Bickel, et al.
Epilepsia
|
August 5, 2025
Evidence demands action: An invitation to share the burden of proof
Danielle 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 humans
Douglas 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 disability
Daphné 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 humans
Douglas 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 epilepsy
Iris 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 Variants
Maria Carla Borroto, Coralie Michaud, Chloé Hudon, et al.
Page
of 68