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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
April 25, 2019
Antagonizing Increased <i>miR-135a</i> Levels at the Chronic Stage of Experimental TLE Reduces Spontaneous Recurrent Seizures
Vamshidhar R Vangoor, Cristina R Reschke, Ketharini Senthilkumar, et al.
Nature Communications
|
September 4, 2015
Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures
Tommy Stödberg, Amy McTague, Arnaud J Ruiz, et al.
Science Translational Medicine
|
May 20, 2021
Gene therapy restores dopamine transporter expression and ameliorates pathology in iPSC and mouse models of infantile parkinsonism
Joanne Ng, Serena Barral, Carmen De La Fuente Barrigon, et al.
Epilepsia
|
February 25, 2020
Biological concepts in human sodium channel epilepsies and their relevance in clinical practice
Andreas Brunklaus, Juanjiangmeng Du, Felix Steckler, et al.
Epilepsy & Behavior : E&B
|
September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part I: Clinical and network analysis approaches
Felix Rosenow, Natascha van Alphen, Albert Becker, et al.
Epilepsy & Behavior : E&B
|
September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part II: Experimental and translational approaches
Sebastian Bauer, Natascha van Alphen, Albert Becker, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 26, 2020
A systems approach delivers a functional microRNA catalog and expanded targets for seizure suppression in temporal lobe epilepsy
Morten T Venø, Cristina R Reschke, Gareth Morris, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification
Tobias Brünger, Ilona Krey, Suyeon Kim, et al.
The Lancet. Neurology
|
July 24, 2018
Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control study
Patrick May, Simon Girard, Merle Harrer, et al.
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of 7
Search research articles
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Showing results (61-70 of 69) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 69 results.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
April 25, 2019
Antagonizing Increased <i>miR-135a</i> Levels at the Chronic Stage of Experimental TLE Reduces Spontaneous Recurrent Seizures
Vamshidhar R Vangoor, Cristina R Reschke, Ketharini Senthilkumar, et al.
Nature Communications
|
September 4, 2015
Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures
Tommy Stödberg, Amy McTague, Arnaud J Ruiz, et al.
Science Translational Medicine
|
May 20, 2021
Gene therapy restores dopamine transporter expression and ameliorates pathology in iPSC and mouse models of infantile parkinsonism
Joanne Ng, Serena Barral, Carmen De La Fuente Barrigon, et al.
Epilepsia
|
February 25, 2020
Biological concepts in human sodium channel epilepsies and their relevance in clinical practice
Andreas Brunklaus, Juanjiangmeng Du, Felix Steckler, et al.
Epilepsy & Behavior : E&B
|
September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part I: Clinical and network analysis approaches
Felix Rosenow, Natascha van Alphen, Albert Becker, et al.
Epilepsy & Behavior : E&B
|
September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part II: Experimental and translational approaches
Sebastian Bauer, Natascha van Alphen, Albert Becker, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 26, 2020
A systems approach delivers a functional microRNA catalog and expanded targets for seizure suppression in temporal lobe epilepsy
Morten T Venø, Cristina R Reschke, Gareth Morris, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification
Tobias Brünger, Ilona Krey, Suyeon Kim, et al.
The Lancet. Neurology
|
July 24, 2018
Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control study
Patrick May, Simon Girard, Merle Harrer, et al.
Page
of 7