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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.
Annals of Neurology
|
October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1
Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
Epilepsia
|
February 18, 2025
Amitriptyline use in individuals with KCNQ2/3 gain-of-function variants: A retrospective cohort study
Matthias De Wachter, Charissa Millevert, Joost Nicolai, et al.
Brain : a Journal of Neurology
|
June 5, 2026
Kv7.2 loss-of-function causes early hyperexcitability and network remodelling
Nina Dirkx, Marcus Kaji, Els De Vriendt, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 5, 2019
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study
Roberto Di Marco, Ann Hallemans, Giulia Bellon, et al.
Epilepsia
|
August 6, 2023
Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo-controlled clinical trial
Joseph Sullivan, Lieven Lagae, J Helen Cross, et al.
Lancet (London, England)
|
December 22, 2019
Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial
Lieven Lagae, Joseph Sullivan, Kelly Knupp, et al.
JAMA Neurology
|
May 2, 2022
Efficacy and Safety of Fenfluramine for the Treatment of Seizures Associated With Lennox-Gastaut Syndrome: A Randomized Clinical Trial
Kelly G Knupp, Ingrid E Scheffer, Berten Ceulemans, et al.
Epilepsia
|
October 5, 2022
Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox-Gastaut syndrome: Interim analysis of an open-label extension study
Kelly G Knupp, Ingrid E Scheffer, Berten Ceulemans, et al.
Human Mutation
|
July 26, 2006
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients
Arvid Suls, Kristl G Claeys, Dirk Goossens, et al.
Page
of 14
Search research articles
Search
Showing results (91-100 of 137) with videos related to
Sort By:
Page
of 14
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.
Annals of Neurology
|
October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1
Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
Epilepsia
|
February 18, 2025
Amitriptyline use in individuals with KCNQ2/3 gain-of-function variants: A retrospective cohort study
Matthias De Wachter, Charissa Millevert, Joost Nicolai, et al.
Brain : a Journal of Neurology
|
June 5, 2026
Kv7.2 loss-of-function causes early hyperexcitability and network remodelling
Nina Dirkx, Marcus Kaji, Els De Vriendt, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 5, 2019
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study
Roberto Di Marco, Ann Hallemans, Giulia Bellon, et al.
Epilepsia
|
August 6, 2023
Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo-controlled clinical trial
Joseph Sullivan, Lieven Lagae, J Helen Cross, et al.
Lancet (London, England)
|
December 22, 2019
Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial
Lieven Lagae, Joseph Sullivan, Kelly Knupp, et al.
JAMA Neurology
|
May 2, 2022
Efficacy and Safety of Fenfluramine for the Treatment of Seizures Associated With Lennox-Gastaut Syndrome: A Randomized Clinical Trial
Kelly G Knupp, Ingrid E Scheffer, Berten Ceulemans, et al.
Epilepsia
|
October 5, 2022
Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox-Gastaut syndrome: Interim analysis of an open-label extension study
Kelly G Knupp, Ingrid E Scheffer, Berten Ceulemans, et al.
Human Mutation
|
July 26, 2006
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients
Arvid Suls, Kristl G Claeys, Dirk Goossens, et al.
Page
of 14