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Anne de Saint-Martin

Showing results (41-50 of 80) with videos related to

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Pediatric Neurology|August 2, 2024
Copy Number Variation and Epilepsy: State of the Art in the Era of High-Throughput Sequencing-A Multicenter Cohort StudySarah Baer, Audrey Schalk, Marguerite Miguet, et al.
The Lancet. Neurology|December 11, 2023
Corticosteroids versus clobazam for treatment of children with epileptic encephalopathy with spike-wave activation in sleep (RESCUE ESES): a multicentre randomised controlled trialMarleen M L van Arnhem, Bart van den Munckhof, Alexis Arzimanoglou, et al.
Brain : a Journal of Neurology|September 19, 2019
KCNT1 epilepsy with migrating focal seizures shows a temporal sequence with poor outcome, high mortality and SUDEPMathieu Kuchenbuch, Giulia Barcia, Nicole Chemaly, et al.
Clinical Genetics|November 13, 2022
Putative founder effect of Arg338* AP4M1 (SPG50) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three familiesAurélie Becker, Charlotte Felici, Laëtitia Lambert, et al.
European Journal of Medical Genetics|January 29, 2022
The EPIGENE network: A French initiative to harmonize and improve the nationwide diagnosis of monogenic epilepsiesLionel Arnaud, Marie-Thérèse Abi Warde, Giulia Barcia, et al.
Epilepsy & Behavior : E&B|December 16, 2021
Adaptive behavior and psychiatric comorbidities in KCNB1 encephalopathyClaire Bar, Delphine Breuillard, Mathieu Kuchenbuch, et al.
European Journal of Human Genetics : EJHG|January 8, 2026
Newly identified ARF3 variants strengthen the causal link between Golgi fragmentation and brain malformationsValentina Muto, Giulia Fasano, Francesca Clementina Radio, et al.
Annals of Neurology|April 23, 2015
Intelligence quotient improves after antiepileptic drug withdrawal following pediatric epilepsy surgeryKim Boshuisen, Monique M J van Schooneveld, Cuno S P M Uiterwaal, et al.
Nature Genetics|August 13, 2013
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunctionGaetan Lesca, Gabrielle Rudolf, Nadine Bruneau, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2016
Idiopathic focal epilepsies: the "lost tribe"Deb K Pal, Colin Ferrie, Laura Addis, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Pediatric Neurology|August 2, 2024
Copy Number Variation and Epilepsy: State of the Art in the Era of High-Throughput Sequencing-A Multicenter Cohort StudySarah Baer, Audrey Schalk, Marguerite Miguet, et al.
The Lancet. Neurology|December 11, 2023
Corticosteroids versus clobazam for treatment of children with epileptic encephalopathy with spike-wave activation in sleep (RESCUE ESES): a multicentre randomised controlled trialMarleen M L van Arnhem, Bart van den Munckhof, Alexis Arzimanoglou, et al.
Brain : a Journal of Neurology|September 19, 2019
KCNT1 epilepsy with migrating focal seizures shows a temporal sequence with poor outcome, high mortality and SUDEPMathieu Kuchenbuch, Giulia Barcia, Nicole Chemaly, et al.
Clinical Genetics|November 13, 2022
Putative founder effect of Arg338* AP4M1 (SPG50) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three familiesAurélie Becker, Charlotte Felici, Laëtitia Lambert, et al.
European Journal of Medical Genetics|January 29, 2022
The EPIGENE network: A French initiative to harmonize and improve the nationwide diagnosis of monogenic epilepsiesLionel Arnaud, Marie-Thérèse Abi Warde, Giulia Barcia, et al.
Epilepsy & Behavior : E&B|December 16, 2021
Adaptive behavior and psychiatric comorbidities in KCNB1 encephalopathyClaire Bar, Delphine Breuillard, Mathieu Kuchenbuch, et al.
European Journal of Human Genetics : EJHG|January 8, 2026
Newly identified ARF3 variants strengthen the causal link between Golgi fragmentation and brain malformationsValentina Muto, Giulia Fasano, Francesca Clementina Radio, et al.
Annals of Neurology|April 23, 2015
Intelligence quotient improves after antiepileptic drug withdrawal following pediatric epilepsy surgeryKim Boshuisen, Monique M J van Schooneveld, Cuno S P M Uiterwaal, et al.
Nature Genetics|August 13, 2013
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunctionGaetan Lesca, Gabrielle Rudolf, Nadine Bruneau, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2016
Idiopathic focal epilepsies: the "lost tribe"Deb K Pal, Colin Ferrie, Laura Addis, et al.
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