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Mathieu Milh

Showing results (71-80 of 138) with videos related to

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Epilepsia|April 3, 2020
A knock-in mouse model for KCNQ2-related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairmentMathieu Milh, Pierre Roubertoux, Najoua Biba, et al.
Epilepsy & Behavior : E&B|December 14, 2020
Real-life use of videos in pediatric epilepsy consultationsBlandine Dozières-Puyravel, Louis Dufour, Caroline Hachon Le Camus, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 18, 2015
Severe phenotypic spectrum of biallelic mutations in PRRT2 geneMarion Delcourt, Florence Riant, Josette Mancini, et al.
Epilepsia|June 9, 2025
Broadening the phenotype associated with pathogenic variants in the FGF12 gene: From developmental and epileptic encephalopathy to drug-responsive epilepsy with favorable cognitive outcomeClément Pierret, Florence Riccardi, Julien Neveu, 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 StudyGianluca D'Onofrio, Mathieu Kuchenbuch, Caroline Hachon-Le Camus, et al.
Brain Sciences|August 6, 2021
Expansion of the Genotypic and Phenotypic Spectrum of WASF1-Related Neurodevelopmental DisorderSiddharth Srivastava, Erica L Macke, Lindsay C Swanson, et al.
Journal of Neurology|May 6, 2019
Can histologically normal epileptogenic zone share common electrophysiological phenotypes with focal cortical dysplasia? SEEG-based study in MRI-negative epileptic patientsStanislas Lagarde, Julia Scholly, Irina Popa, et al.
Brain : a Journal of Neurology|September 16, 2008
Key clinical features to identify girls with CDKL5 mutationsNadia Bahi-Buisson, Juliette Nectoux, Haydeé Rosas-Vargas, et al.
Epilepsia|February 18, 2025
Amitriptyline use in individuals with KCNQ2/3 gain-of-function variants: A retrospective cohort studyMatthias De Wachter, Charissa Millevert, Joost Nicolai, et al.
Neurology|April 5, 2015
GRID2 mutations span from congenital to mild adult-onset cerebellar ataxiaMarie Coutelier, Lydie Burglen, Emeline Mundwiller, et al.
Pageof 14

Showing results (71-80 of 138) with videos related to

Sort By:
Pageof 14
Epilepsia|April 3, 2020
A knock-in mouse model for KCNQ2-related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairmentMathieu Milh, Pierre Roubertoux, Najoua Biba, et al.
Epilepsy & Behavior : E&B|December 14, 2020
Real-life use of videos in pediatric epilepsy consultationsBlandine Dozières-Puyravel, Louis Dufour, Caroline Hachon Le Camus, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 18, 2015
Severe phenotypic spectrum of biallelic mutations in PRRT2 geneMarion Delcourt, Florence Riant, Josette Mancini, et al.
Epilepsia|June 9, 2025
Broadening the phenotype associated with pathogenic variants in the FGF12 gene: From developmental and epileptic encephalopathy to drug-responsive epilepsy with favorable cognitive outcomeClément Pierret, Florence Riccardi, Julien Neveu, 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 StudyGianluca D'Onofrio, Mathieu Kuchenbuch, Caroline Hachon-Le Camus, et al.
Brain Sciences|August 6, 2021
Expansion of the Genotypic and Phenotypic Spectrum of WASF1-Related Neurodevelopmental DisorderSiddharth Srivastava, Erica L Macke, Lindsay C Swanson, et al.
Journal of Neurology|May 6, 2019
Can histologically normal epileptogenic zone share common electrophysiological phenotypes with focal cortical dysplasia? SEEG-based study in MRI-negative epileptic patientsStanislas Lagarde, Julia Scholly, Irina Popa, et al.
Brain : a Journal of Neurology|September 16, 2008
Key clinical features to identify girls with CDKL5 mutationsNadia Bahi-Buisson, Juliette Nectoux, Haydeé Rosas-Vargas, et al.
Epilepsia|February 18, 2025
Amitriptyline use in individuals with KCNQ2/3 gain-of-function variants: A retrospective cohort studyMatthias De Wachter, Charissa Millevert, Joost Nicolai, et al.
Neurology|April 5, 2015
GRID2 mutations span from congenital to mild adult-onset cerebellar ataxiaMarie Coutelier, Lydie Burglen, Emeline Mundwiller, et al.
Pageof 14