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Human Mutation
|
February 5, 2009
Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy
Cécile Saint-Martin, Grégory Gauvain, Georgeta Teodorescu, et al.
JAMA Neurology
|
December 3, 2019
Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens: A Randomized Clinical Trial
Rima Nabbout, Arun Mistry, Sameer Zuberi, et al.
Epilepsia
|
March 12, 2025
Long-term safety and effectiveness of fenfluramine in children and adults with Dravet syndrome
Ingrid E Scheffer, Rima Nabbout, Lieven Lagae, et al.
Epilepsy Research
|
October 21, 2022
EEG parameters as endpoints in epilepsy clinical trials - An expert panel opinion paper
Jeffrey Buchhalter, Caroline Neuray, Jocelyn Y Cheng, et al.
Frontiers in Neurology
|
September 9, 2020
Slow Titration of Cannabidiol Add-On in Drug-Resistant Epilepsies Can Improve Safety With Maintained Efficacy in an Open-Label Study
Gianluca D'Onofrio, Mathieu Kuchenbuch, Caroline Hachon-Le Camus, et al.
Epilepsia Open
|
December 18, 2020
Complete hemispherotomy leads to lateralized functional organization and lower level of consciousness in the isolated hemisphere
Thomas Blauwblomme, Athena Demertzi, Jean-Marc Tacchela, et al.
The Journal of Pediatrics
|
February 28, 2021
Fetal Brain Magnetic Resonance Imaging Findings Predict Neurodevelopment in Children with Tuberous Sclerosis Complex
Hanna M Hulshof, Emma M H Slot, Maarten Lequin, et al.
Epilepsy & Behavior : E&B
|
August 5, 2021
Treatment with fenfluramine in patients with Dravet syndrome has no long-term effects on weight and growth
Antonio Gil-Nagel, Joseph Sullivan, Berten Ceulemans, et al.
Neurology. Genetics
|
April 12, 2016
Novel GABRG2 mutations cause familial febrile seizures
Morgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Epilepsia
|
February 14, 2016
Epilepsy in young Tsc1(+/-) mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex
Svetlana Gataullina, Eric Lemaire, Fabrice Wendling, et al.
Page
of 31
Search research articles
Search
Showing results (201-210 of 310) with videos related to
Sort By:
Page
of 31
Human Mutation
|
February 5, 2009
Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy
Cécile Saint-Martin, Grégory Gauvain, Georgeta Teodorescu, et al.
JAMA Neurology
|
December 3, 2019
Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens: A Randomized Clinical Trial
Rima Nabbout, Arun Mistry, Sameer Zuberi, et al.
Epilepsia
|
March 12, 2025
Long-term safety and effectiveness of fenfluramine in children and adults with Dravet syndrome
Ingrid E Scheffer, Rima Nabbout, Lieven Lagae, et al.
Epilepsy Research
|
October 21, 2022
EEG parameters as endpoints in epilepsy clinical trials - An expert panel opinion paper
Jeffrey Buchhalter, Caroline Neuray, Jocelyn Y Cheng, et al.
Frontiers in Neurology
|
September 9, 2020
Slow Titration of Cannabidiol Add-On in Drug-Resistant Epilepsies Can Improve Safety With Maintained Efficacy in an Open-Label Study
Gianluca D'Onofrio, Mathieu Kuchenbuch, Caroline Hachon-Le Camus, et al.
Epilepsia Open
|
December 18, 2020
Complete hemispherotomy leads to lateralized functional organization and lower level of consciousness in the isolated hemisphere
Thomas Blauwblomme, Athena Demertzi, Jean-Marc Tacchela, et al.
The Journal of Pediatrics
|
February 28, 2021
Fetal Brain Magnetic Resonance Imaging Findings Predict Neurodevelopment in Children with Tuberous Sclerosis Complex
Hanna M Hulshof, Emma M H Slot, Maarten Lequin, et al.
Epilepsy & Behavior : E&B
|
August 5, 2021
Treatment with fenfluramine in patients with Dravet syndrome has no long-term effects on weight and growth
Antonio Gil-Nagel, Joseph Sullivan, Berten Ceulemans, et al.
Neurology. Genetics
|
April 12, 2016
Novel GABRG2 mutations cause familial febrile seizures
Morgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Epilepsia
|
February 14, 2016
Epilepsy in young Tsc1(+/-) mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex
Svetlana Gataullina, Eric Lemaire, Fabrice Wendling, et al.
Page
of 31