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Epilepsia
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December 23, 2023
Developmental epileptic encephalopathy in DLG4-related synaptopathy
Benedetta Kassabian, Amanda M Levy, Elena Gardella, et al.
Epilepsia
|
February 27, 2024
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study
Rebecca Kerestes, Andrew Perry, Lucy Vivash, et al.
American Journal of Human Genetics
|
July 19, 2023
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
Daniel G Calame, Tianyu Guo, Chen Wang, et al.
Human Brain Mapping
|
May 30, 2020
The ENIGMA-Epilepsy working group: Mapping disease from large data sets
Sanjay M Sisodiya, Christopher D Whelan, Sean N Hatton, et al.
Nature Communications
|
July 27, 2022
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression
Sara Larivière, Jessica Royer, Raúl Rodríguez-Cruces, et al.
Epilepsia
|
January 28, 2026
Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants
Sebastian Ortiz, Leonardo Affronte, Chiara Bagliani, et al.
Biorxiv : the Preprint Server for Biology
|
June 22, 2026
Sex-related structural alterations across common epilepsies: a worldwide ENIGMA study
Huantao Wen, Bin Wan, Taha Gholipour, et al.
Brain : a Journal of Neurology
|
August 11, 2022
Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study
Hannah Spitzer, Mathilde Ripart, Kirstie Whitaker, et al.
JAMA Neurology
|
February 24, 2025
Detection of Epileptogenic Focal Cortical Dysplasia Using Graph Neural Networks: A MELD Study
Mathilde Ripart, Hannah Spitzer, Logan Z J Williams, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 29, 2018
Correction: The landscape of epilepsy-related GATOR1 variants
Sara Baldassari, Fabienne Picard, Nienke E Verbeek, et al.
Page
of 62
Search research articles
Search
Showing results (581-590 of 611) with videos related to
Sort By:
Page
of 62
Epilepsia
|
December 23, 2023
Developmental epileptic encephalopathy in DLG4-related synaptopathy
Benedetta Kassabian, Amanda M Levy, Elena Gardella, et al.
Epilepsia
|
February 27, 2024
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study
Rebecca Kerestes, Andrew Perry, Lucy Vivash, et al.
American Journal of Human Genetics
|
July 19, 2023
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
Daniel G Calame, Tianyu Guo, Chen Wang, et al.
Human Brain Mapping
|
May 30, 2020
The ENIGMA-Epilepsy working group: Mapping disease from large data sets
Sanjay M Sisodiya, Christopher D Whelan, Sean N Hatton, et al.
Nature Communications
|
July 27, 2022
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression
Sara Larivière, Jessica Royer, Raúl Rodríguez-Cruces, et al.
Epilepsia
|
January 28, 2026
Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants
Sebastian Ortiz, Leonardo Affronte, Chiara Bagliani, et al.
Biorxiv : the Preprint Server for Biology
|
June 22, 2026
Sex-related structural alterations across common epilepsies: a worldwide ENIGMA study
Huantao Wen, Bin Wan, Taha Gholipour, et al.
Brain : a Journal of Neurology
|
August 11, 2022
Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study
Hannah Spitzer, Mathilde Ripart, Kirstie Whitaker, et al.
JAMA Neurology
|
February 24, 2025
Detection of Epileptogenic Focal Cortical Dysplasia Using Graph Neural Networks: A MELD Study
Mathilde Ripart, Hannah Spitzer, Logan Z J Williams, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 29, 2018
Correction: The landscape of epilepsy-related GATOR1 variants
Sara Baldassari, Fabienne Picard, Nienke E Verbeek, et al.
Page
of 62