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Sameer Zuberi

Showing results (21-30 of 36) with videos related to

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Archives of Disease in Childhood|October 20, 2018
Surveillance for variant CJD: should more children with neurodegenerative diseases have autopsies?Christopher Verity, Anne Marie Winstone, Robert Will, et al.
JAMA Neurology|December 3, 2019
Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens: A Randomized Clinical TrialRima Nabbout, Arun Mistry, Sameer Zuberi, et al.
Neurology|July 27, 2018
Glutamate receptor δ2 serum antibodies in pediatric opsoclonus myoclonus ataxia syndromeGeorgina Berridge, David A Menassa, Teresa Moloney, et al.
Frontiers in Neurology|July 7, 2022
International Consensus Recommendations for the Assessment and Management of Individuals With CDKL5 Deficiency DisorderSam Amin, Marie Monaghan, Angel Aledo-Serrano, et al.
Epilepsia|November 23, 2007
Spectrum of epilepsy in terminal 1p36 deletion syndromeNadia Bahi-Buisson, Eva Guttierrez-Delicado, Christine Soufflet, et al.
Brain : a Journal of Neurology|April 3, 2023
Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' conditionHelena Martins Custodio, Lisa M Clayton, Ravishankara Bellampalli, et al.
Epilepsia|July 30, 2019
Classification as autonomic versus sensory seizuresRobert S Fisher, Helen Cross, Carol D'Souza, et al.
Epilepsia|May 11, 2019
2017 International League Against Epilepsy classifications of seizures and epilepsy are steps in the right directionRobert S Fisher, Helen Cross, Carol D'Souza, et al.
Seizure|January 22, 2025
Top Ten epilepsy research priorities: A UK priority setting partnershipAnna C Norton, Caoimhe Twohig-Bennett, Maxine Smeaton, et al.
Epilepsia|November 18, 2025
Cognitive stagnation and executive function deficits in young children with SCN1A+ Dravet syndrome: Detailed characterization of onset, progression, and impact in the ENVISION natural history studyJoseph Sullivan, M Scott Perry, Ingrid E Scheffer, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Archives of Disease in Childhood|October 20, 2018
Surveillance for variant CJD: should more children with neurodegenerative diseases have autopsies?Christopher Verity, Anne Marie Winstone, Robert Will, et al.
JAMA Neurology|December 3, 2019
Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens: A Randomized Clinical TrialRima Nabbout, Arun Mistry, Sameer Zuberi, et al.
Neurology|July 27, 2018
Glutamate receptor δ2 serum antibodies in pediatric opsoclonus myoclonus ataxia syndromeGeorgina Berridge, David A Menassa, Teresa Moloney, et al.
Frontiers in Neurology|July 7, 2022
International Consensus Recommendations for the Assessment and Management of Individuals With CDKL5 Deficiency DisorderSam Amin, Marie Monaghan, Angel Aledo-Serrano, et al.
Epilepsia|November 23, 2007
Spectrum of epilepsy in terminal 1p36 deletion syndromeNadia Bahi-Buisson, Eva Guttierrez-Delicado, Christine Soufflet, et al.
Brain : a Journal of Neurology|April 3, 2023
Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' conditionHelena Martins Custodio, Lisa M Clayton, Ravishankara Bellampalli, et al.
Epilepsia|July 30, 2019
Classification as autonomic versus sensory seizuresRobert S Fisher, Helen Cross, Carol D'Souza, et al.
Epilepsia|May 11, 2019
2017 International League Against Epilepsy classifications of seizures and epilepsy are steps in the right directionRobert S Fisher, Helen Cross, Carol D'Souza, et al.
Seizure|January 22, 2025
Top Ten epilepsy research priorities: A UK priority setting partnershipAnna C Norton, Caoimhe Twohig-Bennett, Maxine Smeaton, et al.
Epilepsia|November 18, 2025
Cognitive stagnation and executive function deficits in young children with SCN1A+ Dravet syndrome: Detailed characterization of onset, progression, and impact in the ENVISION natural history studyJoseph Sullivan, M Scott Perry, Ingrid E Scheffer, et al.
Pageof 4