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Annals of Clinical and Translational Neurology
|
May 23, 2026
White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy
Amanda G Sandoval Karamian, Tianjia Zhu, Hao Huang, et al.
Frontiers in Neurology
|
April 20, 2023
Investigating the genetic contribution in febrile infection-related epilepsy syndrome and refractory status epilepticus
Danielle deCampo, Julie Xian, Alexis Karlin, et al.
Epilepsia
|
November 11, 2025
Clinical trajectories and medication response in TBC1D24-related epilepsies
Ealing Mondragon, Jan H Magielski, Bintou Bane, et al.
Epilepsia
|
January 28, 2016
Seizures as presenting and prominent symptom in chorea-acanthocytosis with c.2343del VPS13A gene mutation
Felix Benninger, Zaid Afawi, Amos D Korczyn, et al.
Genetics in Medicine Open
|
June 3, 2024
Clinical variants in <i>Caenorhabditis elegans</i> expressing human STXBP1 reveal a novel class of pathogenic variants and classify variants of uncertain significance
Christopher E Hopkins, Kathryn McCormick, Trisha Brock, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 10, 2026
Monogenic epilepsies exhibit distinct sleep endophenotypes
Katharina S Bochtler, Alexander I Batterman, Hyun Yong Koh, et al.
Developmental Medicine and Child Neurology
|
May 20, 2024
Child neurology telemedicine: Analyzing 14 820 patient encounters during the first year of the COVID-19 pandemic
Michael C Kaufman, Julie Xian, Peter D Galer, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
November 20, 2008
Obstetric events as a risk factor for febrile seizures: a community-based twin study
Ingo Helbig, Kate M Lawrence, Mary M Connellan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 9, 2024
A structurally precise mechanism links an epilepsy-associated <i>KCNC2</i> potassium channel mutation to interneuron dysfunction
Jerome Clatot, Christopher B Currin, Qiansheng Liang, et al.
Journal of Child Neurology
|
November 22, 2013
Broad phenotypic heterogeneity due to a novel SCN1A mutation in a family with genetic epilepsy with febrile seizures plus
Hadassa Goldberg-Stern, Sharon Aharoni, Zaid Afawi, et al.
Page
of 30
Search research articles
Search
Showing results (81-90 of 294) with videos related to
Sort By:
Page
of 30
Annals of Clinical and Translational Neurology
|
May 23, 2026
White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy
Amanda G Sandoval Karamian, Tianjia Zhu, Hao Huang, et al.
Frontiers in Neurology
|
April 20, 2023
Investigating the genetic contribution in febrile infection-related epilepsy syndrome and refractory status epilepticus
Danielle deCampo, Julie Xian, Alexis Karlin, et al.
Epilepsia
|
November 11, 2025
Clinical trajectories and medication response in TBC1D24-related epilepsies
Ealing Mondragon, Jan H Magielski, Bintou Bane, et al.
Epilepsia
|
January 28, 2016
Seizures as presenting and prominent symptom in chorea-acanthocytosis with c.2343del VPS13A gene mutation
Felix Benninger, Zaid Afawi, Amos D Korczyn, et al.
Genetics in Medicine Open
|
June 3, 2024
Clinical variants in <i>Caenorhabditis elegans</i> expressing human STXBP1 reveal a novel class of pathogenic variants and classify variants of uncertain significance
Christopher E Hopkins, Kathryn McCormick, Trisha Brock, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 10, 2026
Monogenic epilepsies exhibit distinct sleep endophenotypes
Katharina S Bochtler, Alexander I Batterman, Hyun Yong Koh, et al.
Developmental Medicine and Child Neurology
|
May 20, 2024
Child neurology telemedicine: Analyzing 14 820 patient encounters during the first year of the COVID-19 pandemic
Michael C Kaufman, Julie Xian, Peter D Galer, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
November 20, 2008
Obstetric events as a risk factor for febrile seizures: a community-based twin study
Ingo Helbig, Kate M Lawrence, Mary M Connellan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 9, 2024
A structurally precise mechanism links an epilepsy-associated <i>KCNC2</i> potassium channel mutation to interneuron dysfunction
Jerome Clatot, Christopher B Currin, Qiansheng Liang, et al.
Journal of Child Neurology
|
November 22, 2013
Broad phenotypic heterogeneity due to a novel SCN1A mutation in a family with genetic epilepsy with febrile seizures plus
Hadassa Goldberg-Stern, Sharon Aharoni, Zaid Afawi, et al.
Page
of 30