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Edouard Hirsch

Showing results (101-110 of 128) with videos related to

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Epilepsia|July 6, 2017
Response to the numbering of seizure typesRobert S Fisher, J Helen Cross, Carol D'Souza, 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.
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.
Human Genetics|July 3, 2016
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2Lyndal Henden, Saskia Freytag, Zaid Afawi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 8, 2021
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patientsMarie Le Roux, Magalie Barth, Sophie Gueden, et al.
Human Molecular Genetics|February 19, 2015
Galanin pathogenic mutations in temporal lobe epilepsyMichel Guipponi, Amina Chentouf, Kristin E B Webling, et al.
European Journal of Human Genetics : EJHG|May 30, 2020
Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesiaDiane Doummar, Christel Dentel, Romane Lyautey, et al.
Seizure|May 17, 2020
EEG in fitness to drive evaluations in people with epilepsy - Considerable variations across EuropeRune Markhus, Oliver Henning, Ellen Molteberg, et al.
Seizure|April 23, 2016
Current practices in long-term video-EEG monitoring services: A survey among partners of the E-PILEPSY pilot network of reference for refractory epilepsy and epilepsy surgeryTeia Kobulashvili, Julia Höfler, Judith Dobesberger, et al.
Brain : a Journal of Neurology|December 14, 2018
GRIN2A-related disorders: genotype and functional consequence predict phenotypeVincent Strehlow, Henrike O Heyne, Danique R M Vlaskamp, et al.
Pageof 13

Showing results (101-110 of 128) with videos related to

Sort By:
Pageof 13
Epilepsia|July 6, 2017
Response to the numbering of seizure typesRobert S Fisher, J Helen Cross, Carol D'Souza, 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.
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.
Human Genetics|July 3, 2016
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2Lyndal Henden, Saskia Freytag, Zaid Afawi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 8, 2021
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patientsMarie Le Roux, Magalie Barth, Sophie Gueden, et al.
Human Molecular Genetics|February 19, 2015
Galanin pathogenic mutations in temporal lobe epilepsyMichel Guipponi, Amina Chentouf, Kristin E B Webling, et al.
European Journal of Human Genetics : EJHG|May 30, 2020
Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesiaDiane Doummar, Christel Dentel, Romane Lyautey, et al.
Seizure|May 17, 2020
EEG in fitness to drive evaluations in people with epilepsy - Considerable variations across EuropeRune Markhus, Oliver Henning, Ellen Molteberg, et al.
Seizure|April 23, 2016
Current practices in long-term video-EEG monitoring services: A survey among partners of the E-PILEPSY pilot network of reference for refractory epilepsy and epilepsy surgeryTeia Kobulashvili, Julia Höfler, Judith Dobesberger, et al.
Brain : a Journal of Neurology|December 14, 2018
GRIN2A-related disorders: genotype and functional consequence predict phenotypeVincent Strehlow, Henrike O Heyne, Danique R M Vlaskamp, et al.
Pageof 13