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Rima Nabbout

Showing results (71-80 of 310) with videos related to

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Epilepsy Research|June 10, 2008
An unexpected EEG course in Dravet syndromeRima Nabbout, Isabelle Desguerre, Sandra Sabbagh, et al.
Epilepsia|May 17, 2011
Ketogenic diet also benefits Dravet syndrome patients receiving stiripentol: a prospective pilot studyRima Nabbout, Cristiana Copioli, Mathilde Chipaux, et al.
Epilepsy & Behavior : E&B|January 14, 2024
Transition in epilepsy - A pilot study with patients in and outside of academic centersQuratulain Zulfiqar Ali, Paula Marques, Puja Patel, et al.
Orphanet Journal of Rare Diseases|September 1, 2023
Composite endpoints, including patient reported outcomes, in rare diseasesJohan Verbeeck, Maya Dirani, Johann W Bauer, et al.
Epilepsia|January 7, 2020
Dravet syndrome: Treatment options and management of prolonged seizuresJ Helen Cross, Roberto H Caraballo, Rima Nabbout, et al.
Epilepsy & Behavior : E&B|January 11, 2019
The evaluation and costs of transition programs for youth with epilepsyRima Nabbout, Alexis Arzimanoglou, Richard F M Chin, et al.
Clinical Genetics|June 7, 2019
Exome sequencing findings in 27 patients with myoclonic-atonic epilepsy: Is there a major genetic factor?Laura Routier, Florine Verny, Giulia Barcia, et al.
Epilepsy & Behavior : E&B|July 7, 2017
Age-related "Sleep/nocturnal" tonic and tonic clonic seizure clusters are underdiagnosed in patients with Dravet SyndromeEmma Losito, Matthieu Kuchenbuch, Nicole Chemaly, et al.
Epilepsy Research|January 15, 2019
Pharmacokinetic evaluation of vigabatrin dose for the treatment of refractory focal seizures in children using adult and pediatric dataChristelle Rodrigues, Catherine Chiron, Marwa Ounissi, et al.
Epilepsia|December 25, 2018
Long-term cannabidiol treatment in patients with Dravet syndrome: An open-label extension trialOrrin Devinsky, Rima Nabbout, Ian Miller, et al.
Pageof 31

Showing results (71-80 of 310) with videos related to

Sort By:
Pageof 31
Epilepsy Research|June 10, 2008
An unexpected EEG course in Dravet syndromeRima Nabbout, Isabelle Desguerre, Sandra Sabbagh, et al.
Epilepsia|May 17, 2011
Ketogenic diet also benefits Dravet syndrome patients receiving stiripentol: a prospective pilot studyRima Nabbout, Cristiana Copioli, Mathilde Chipaux, et al.
Epilepsy & Behavior : E&B|January 14, 2024
Transition in epilepsy - A pilot study with patients in and outside of academic centersQuratulain Zulfiqar Ali, Paula Marques, Puja Patel, et al.
Orphanet Journal of Rare Diseases|September 1, 2023
Composite endpoints, including patient reported outcomes, in rare diseasesJohan Verbeeck, Maya Dirani, Johann W Bauer, et al.
Epilepsia|January 7, 2020
Dravet syndrome: Treatment options and management of prolonged seizuresJ Helen Cross, Roberto H Caraballo, Rima Nabbout, et al.
Epilepsy & Behavior : E&B|January 11, 2019
The evaluation and costs of transition programs for youth with epilepsyRima Nabbout, Alexis Arzimanoglou, Richard F M Chin, et al.
Clinical Genetics|June 7, 2019
Exome sequencing findings in 27 patients with myoclonic-atonic epilepsy: Is there a major genetic factor?Laura Routier, Florine Verny, Giulia Barcia, et al.
Epilepsy & Behavior : E&B|July 7, 2017
Age-related "Sleep/nocturnal" tonic and tonic clonic seizure clusters are underdiagnosed in patients with Dravet SyndromeEmma Losito, Matthieu Kuchenbuch, Nicole Chemaly, et al.
Epilepsy Research|January 15, 2019
Pharmacokinetic evaluation of vigabatrin dose for the treatment of refractory focal seizures in children using adult and pediatric dataChristelle Rodrigues, Catherine Chiron, Marwa Ounissi, et al.
Epilepsia|December 25, 2018
Long-term cannabidiol treatment in patients with Dravet syndrome: An open-label extension trialOrrin Devinsky, Rima Nabbout, Ian Miller, et al.
Pageof 31