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Showing results (61-70 of 90) with videos related to
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Epilepsia
|
January 5, 2026
Memantine treatment in individuals with GRIN gain-of-function variants is associated with improvements in behavior, development, and seizure frequency
Maike Karnstedt, Riley E Perszyk, Scott J Myers, et al.
Infection
|
February 23, 2023
First detected geographical cluster of BoDV-1 encephalitis from same small village in two children: therapeutic considerations and epidemiological implications
Leonie Grosse, Victoria Lieftüchter, Yannik Vollmuth, et al.
Nature Medicine
|
April 22, 2025
Antisense oligonucleotide treatment in a preterm infant with early-onset SCN2A developmental and epileptic encephalopathy
Matias Wagner, Géza Berecki, Walid Fazeli, et al.
Translational Neuroscience
|
January 29, 2024
Brain expression profiles of two <i>SCN1A</i> antisense RNAs in children and adolescents with epilepsy
Marius Frederik Schneider, Miriam Vogt, Johanna Scheuermann, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
June 11, 2026
Epilepsy surgery in pediatric patients with complex COL4A1/2-associated epilepsy
Jan P Nieke, Ingrid Koerber-Rosso, Lena-Luise Becker, et al.
Brain & Development
|
October 24, 2015
LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs
Saskia M Herbst, Christiane R Proepper, Tobias Geis, et al.
Nature Genetics
|
February 28, 2018
Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy
Daniel Kotlarz, Benjamin Marquardt, Tuva Barøy, et al.
Brain : a Journal of Neurology
|
September 30, 2021
Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset
Nazanin Mirza-Schreiber, Michael Zech, Rory Wilson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 27, 2021
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies
Simona Balestrini, Daniela Chiarello, Maria Gogou, et al.
American Journal of Human Genetics
|
January 17, 2025
Bi-allelic KICS2 mutations impair KICSTOR complex-mediated mTORC1 regulation, causing intellectual disability and epilepsy
Rebecca Buchert, Martin D Burkhalter, Chrisovalantou Huridou, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 90) with videos related to
Sort By:
Page
of 9
Epilepsia
|
January 5, 2026
Memantine treatment in individuals with GRIN gain-of-function variants is associated with improvements in behavior, development, and seizure frequency
Maike Karnstedt, Riley E Perszyk, Scott J Myers, et al.
Infection
|
February 23, 2023
First detected geographical cluster of BoDV-1 encephalitis from same small village in two children: therapeutic considerations and epidemiological implications
Leonie Grosse, Victoria Lieftüchter, Yannik Vollmuth, et al.
Nature Medicine
|
April 22, 2025
Antisense oligonucleotide treatment in a preterm infant with early-onset SCN2A developmental and epileptic encephalopathy
Matias Wagner, Géza Berecki, Walid Fazeli, et al.
Translational Neuroscience
|
January 29, 2024
Brain expression profiles of two <i>SCN1A</i> antisense RNAs in children and adolescents with epilepsy
Marius Frederik Schneider, Miriam Vogt, Johanna Scheuermann, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
June 11, 2026
Epilepsy surgery in pediatric patients with complex COL4A1/2-associated epilepsy
Jan P Nieke, Ingrid Koerber-Rosso, Lena-Luise Becker, et al.
Brain & Development
|
October 24, 2015
LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs
Saskia M Herbst, Christiane R Proepper, Tobias Geis, et al.
Nature Genetics
|
February 28, 2018
Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy
Daniel Kotlarz, Benjamin Marquardt, Tuva Barøy, et al.
Brain : a Journal of Neurology
|
September 30, 2021
Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset
Nazanin Mirza-Schreiber, Michael Zech, Rory Wilson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 27, 2021
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies
Simona Balestrini, Daniela Chiarello, Maria Gogou, et al.
American Journal of Human Genetics
|
January 17, 2025
Bi-allelic KICS2 mutations impair KICSTOR complex-mediated mTORC1 regulation, causing intellectual disability and epilepsy
Rebecca Buchert, Martin D Burkhalter, Chrisovalantou Huridou, et al.
Page
of 9