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Rima Nabbout

Showing results (121-130 of 310) with videos related to

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Epilepsy Research|July 9, 2016
Patients with dravet syndrome in the era of stiripentol: A French cohort cross-sectional studyPaola De Liso, Nicole Chemaly, Jacques Laschet, et al.
Epilepsia Open|March 8, 2021
Impact of the COVID-19 lockdown on patients and families with Dravet syndromeIsabella Brambilla, José Ángel Aibar, Anne Sophie Hallet, et al.
European Journal of Medical Genetics|May 26, 2022
Defining causal variants in rare epilepsies: an essential team effort between biomedical scientists, geneticists and epileptologistsAmy McTague, Andreas Brunklaus, Giulia Barcia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2021
Deep phenotyping unstructured data mining in an extensive pediatric database to unravel a common KCNA2 variant in neurodevelopmental syndromesMarie Hully, Tommaso Lo Barco, Anna Kaminska, et al.
Developmental Medicine and Child Neurology|August 23, 2014
Seizures and epilepsy in hypoglycaemia caused by inborn errors of metabolismSvetlana Gataullina, Pascale Delonlay, Eric Lemaire, et al.
The New England Journal of Medicine|May 25, 2017
Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet SyndromeOrrin Devinsky, J Helen Cross, Linda Laux, et al.
Orphanet Journal of Rare Diseases|January 23, 2020
A systematic review on the burden of illness in individuals with tuberous sclerosis complex (TSC)Johann Philipp Zöllner, David Neal Franz, Christoph Hertzberg, et al.
Epilepsia Open|November 8, 2021
A European pilot study in Dravet Syndrome to delineate what really matters for the patients and familiesNicole Chemaly, Mathieu Kuchenbuch, Théo Teng, et al.
Orphanet Journal of Rare Diseases|December 20, 2024
Multi-stakeholder sessions on major innovation topics in rare disease clinical trialsDaniel Bodden, Stefanie Schoenen, Stephanie Wied, et al.
European Journal of Medical Genetics|October 18, 2024
Exploring the clinical spectrum of CNTNAP2-related neurodevelopmental disorders: A case series and a literature appraisalGiulia Barcia, Giovanna Scorrano, Marlène Rio, et al.
Pageof 31

Showing results (121-130 of 310) with videos related to

Sort By:
Pageof 31
Epilepsy Research|July 9, 2016
Patients with dravet syndrome in the era of stiripentol: A French cohort cross-sectional studyPaola De Liso, Nicole Chemaly, Jacques Laschet, et al.
Epilepsia Open|March 8, 2021
Impact of the COVID-19 lockdown on patients and families with Dravet syndromeIsabella Brambilla, José Ángel Aibar, Anne Sophie Hallet, et al.
European Journal of Medical Genetics|May 26, 2022
Defining causal variants in rare epilepsies: an essential team effort between biomedical scientists, geneticists and epileptologistsAmy McTague, Andreas Brunklaus, Giulia Barcia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2021
Deep phenotyping unstructured data mining in an extensive pediatric database to unravel a common KCNA2 variant in neurodevelopmental syndromesMarie Hully, Tommaso Lo Barco, Anna Kaminska, et al.
Developmental Medicine and Child Neurology|August 23, 2014
Seizures and epilepsy in hypoglycaemia caused by inborn errors of metabolismSvetlana Gataullina, Pascale Delonlay, Eric Lemaire, et al.
The New England Journal of Medicine|May 25, 2017
Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet SyndromeOrrin Devinsky, J Helen Cross, Linda Laux, et al.
Orphanet Journal of Rare Diseases|January 23, 2020
A systematic review on the burden of illness in individuals with tuberous sclerosis complex (TSC)Johann Philipp Zöllner, David Neal Franz, Christoph Hertzberg, et al.
Epilepsia Open|November 8, 2021
A European pilot study in Dravet Syndrome to delineate what really matters for the patients and familiesNicole Chemaly, Mathieu Kuchenbuch, Théo Teng, et al.
Orphanet Journal of Rare Diseases|December 20, 2024
Multi-stakeholder sessions on major innovation topics in rare disease clinical trialsDaniel Bodden, Stefanie Schoenen, Stephanie Wied, et al.
European Journal of Medical Genetics|October 18, 2024
Exploring the clinical spectrum of CNTNAP2-related neurodevelopmental disorders: A case series and a literature appraisalGiulia Barcia, Giovanna Scorrano, Marlène Rio, et al.
Pageof 31