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Sameer M Zuberi

Showing results (51-60 of 123) with videos related to

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Epilepsia|February 5, 2023
Comorbidities and predictors of health-related quality of life in Dravet syndrome: A 10-year, prospective follow-up studyPhoebe Makiello, Tony Feng, Benjamin Dunwoody, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 16, 2025
Trauma, coping, and adjustment when parenting a child with Dravet syndromeAnthony Mercier, Liam Dorris, Andreas Brunklaus, et al.
Epilepsia Open|December 9, 2021
Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in EuropeElena Cardenal-Muñoz, Stéphane Auvin, Vicente Villanueva, et al.
Brain Communications|January 17, 2024
Long-term predictors of developmental outcome and disease burden in <i>SCN1A</i>-positive Dravet syndromeTony Feng, Phoebe Makiello, Benjamin Dunwoody, et al.
Epilepsy & Behavior : E&B|April 22, 2017
The humanistic and economic burden of Dravet syndrome on caregivers and families: Implications for future researchMark P Jensen, Andreas Brunklaus, Liam Dorris, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 16, 2010
Hepatic coma culminating in severe brain damage in a child with a SCN1A mutationDaniella Nishri, Lubov Blumkin, Dorit Lev, et al.
Epilepsia|July 15, 2021
Time to onset of cannabidiol treatment effects in Dravet syndrome: Analysis from two randomized controlled trialsJennifer Madan Cohen, Daniel Checketts, Eduardo Dunayevich, 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.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2015
Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 familiesAndreas Brunklaus, Rachael Ellis, Helen Stewart, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 18, 2021
Vaccination and childhood epilepsiesDana Craiu, Zvonka Rener Primec, Lieven Lagae, et al.
Pageof 13

Showing results (51-60 of 123) with videos related to

Sort By:
Pageof 13
Epilepsia|February 5, 2023
Comorbidities and predictors of health-related quality of life in Dravet syndrome: A 10-year, prospective follow-up studyPhoebe Makiello, Tony Feng, Benjamin Dunwoody, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 16, 2025
Trauma, coping, and adjustment when parenting a child with Dravet syndromeAnthony Mercier, Liam Dorris, Andreas Brunklaus, et al.
Epilepsia Open|December 9, 2021
Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in EuropeElena Cardenal-Muñoz, Stéphane Auvin, Vicente Villanueva, et al.
Brain Communications|January 17, 2024
Long-term predictors of developmental outcome and disease burden in <i>SCN1A</i>-positive Dravet syndromeTony Feng, Phoebe Makiello, Benjamin Dunwoody, et al.
Epilepsy & Behavior : E&B|April 22, 2017
The humanistic and economic burden of Dravet syndrome on caregivers and families: Implications for future researchMark P Jensen, Andreas Brunklaus, Liam Dorris, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 16, 2010
Hepatic coma culminating in severe brain damage in a child with a SCN1A mutationDaniella Nishri, Lubov Blumkin, Dorit Lev, et al.
Epilepsia|July 15, 2021
Time to onset of cannabidiol treatment effects in Dravet syndrome: Analysis from two randomized controlled trialsJennifer Madan Cohen, Daniel Checketts, Eduardo Dunayevich, 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.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2015
Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 familiesAndreas Brunklaus, Rachael Ellis, Helen Stewart, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 18, 2021
Vaccination and childhood epilepsiesDana Craiu, Zvonka Rener Primec, Lieven Lagae, et al.
Pageof 13