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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.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 27, 2021
SYNGAP1-DEE: A visual sensitive epilepsyTommaso Lo Barco, Anna Kaminska, Roberta Solazzi, et al.
Epilepsia|December 8, 2018
Quantitative analysis and EEG markers of KCNT1 epilepsy of infancy with migrating focal seizuresMathieu Kuchenbuch, Pascal Benquet, Anna Kaminska, 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.
Neurology. Genetics|February 28, 2025
Acid Ceramidase Deficiency: New Insights on SMA-PME Natural History, Biomarkers, and <i>In Cell</i> Enzyme Activity AssaySilvestre Cuinat, Paul Rollier, Katheryn Grand, et al.
Movement Disorders Clinical Practice|April 7, 2025
STARDEV Study: Neurodevelopmental Trajectory and Long-Term Outcomes of Patients with Startle Disease/HyperekplexiaDiane Pina, Agathe Roubertie, Marie-Aude Spitz, et al.
Epilepsia Open|May 10, 2025
Genetic etiologies with a large NGS panel in a monocentric cohort of 1000 patients with pediatric onset epilepsiesGiulia Barcia, Nicole Chemaly, Stéphanie Gobin-Limballe, et al.
Neurology. Genetics|December 25, 2019
Epilepsy with migrating focal seizures: KCNT1 mutation hotspots and phenotype variabilityGiulia Barcia, Nicole Chemaly, Mathieu Kuchenbuch, et al.
Epilepsia|February 27, 2024
Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsiesDeclan Gallagher, Eduardo Pérez-Palma, Tobias Bruenger, et al.
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