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Sameer M Zuberi

Showing results (41-50 of 123) with videos related to

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Orphanet Journal of Rare Diseases|March 1, 2023
The burden of illness in Lennox-Gastaut syndrome: a systematic literature reviewAdam Strzelczyk, Sameer M Zuberi, Pasquale Striano, et al.
Journal of Child Neurology|April 3, 2009
A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plusJohn H Livingston, J Helen Cross, Ailsa Mclellan, et al.
CNS Drugs|August 7, 2025
Clinically Meaningful Reduction in Drop Seizures in Patients with Lennox-Gastaut Syndrome Treated with Cannabidiol: Post Hoc Analysis of Phase 3 Clinical TrialsNicola Specchio, Stéphane Auvin, Teresa Greco, et al.
The Lancet. Neurology|April 17, 2024
Improving epilepsy diagnosis across the lifespan: approaches and innovationsJacob Pellinen, Emma C Foster, Jo M Wilmshurst, et al.
Epilepsia|March 6, 2013
Treatment of behavioral problems in intellectually disabled adult patients with epilepsyMichael Kerr, Antonio Gil-Nagel, Michael Glynn, et al.
Epilepsia|September 5, 2015
In response: Evaluating the care of a multidisciplinary clinic by using the White Paper "Listening for a change: Medical and social needs of people with intellectual disability who have epilepsy"Mike Kerr, Christine Linehan, Rose Thompson, et al.
Epilepsia|November 8, 2014
A White Paper on the medical and social needs of people with epilepsy and intellectual disability: the Task Force on Intellectual Disabilities and Epilepsy of the International League Against EpilepsyMike Kerr, Christine Linehan, Rose Thompson, et al.
Epilepsia|February 17, 2015
ICD coding for epilepsy: past, present, and future--a report by the International League Against Epilepsy Task Force on ICD codes in epilepsyNathalie Jette, Ettore Beghi, Dale Hesdorffer, et al.
Brain & Development|January 26, 2005
Electro-clinical phenotypes of chromosome disorders associated with epilepsy in the absence of dysmorphismStewart Macleod, Arup Mallik, John L Tolmie, et al.
The Lancet. Neurology|March 22, 2025
Paediatric neurology in Ukraine: a call for helpAlla Nechai, Oxana Nazar, Kevin Rostasy, et al.
Pageof 13

Showing results (41-50 of 123) with videos related to

Sort By:
Pageof 13
Orphanet Journal of Rare Diseases|March 1, 2023
The burden of illness in Lennox-Gastaut syndrome: a systematic literature reviewAdam Strzelczyk, Sameer M Zuberi, Pasquale Striano, et al.
Journal of Child Neurology|April 3, 2009
A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plusJohn H Livingston, J Helen Cross, Ailsa Mclellan, et al.
CNS Drugs|August 7, 2025
Clinically Meaningful Reduction in Drop Seizures in Patients with Lennox-Gastaut Syndrome Treated with Cannabidiol: Post Hoc Analysis of Phase 3 Clinical TrialsNicola Specchio, Stéphane Auvin, Teresa Greco, et al.
The Lancet. Neurology|April 17, 2024
Improving epilepsy diagnosis across the lifespan: approaches and innovationsJacob Pellinen, Emma C Foster, Jo M Wilmshurst, et al.
Epilepsia|March 6, 2013
Treatment of behavioral problems in intellectually disabled adult patients with epilepsyMichael Kerr, Antonio Gil-Nagel, Michael Glynn, et al.
Epilepsia|September 5, 2015
In response: Evaluating the care of a multidisciplinary clinic by using the White Paper "Listening for a change: Medical and social needs of people with intellectual disability who have epilepsy"Mike Kerr, Christine Linehan, Rose Thompson, et al.
Epilepsia|November 8, 2014
A White Paper on the medical and social needs of people with epilepsy and intellectual disability: the Task Force on Intellectual Disabilities and Epilepsy of the International League Against EpilepsyMike Kerr, Christine Linehan, Rose Thompson, et al.
Epilepsia|February 17, 2015
ICD coding for epilepsy: past, present, and future--a report by the International League Against Epilepsy Task Force on ICD codes in epilepsyNathalie Jette, Ettore Beghi, Dale Hesdorffer, et al.
Brain & Development|January 26, 2005
Electro-clinical phenotypes of chromosome disorders associated with epilepsy in the absence of dysmorphismStewart Macleod, Arup Mallik, John L Tolmie, et al.
The Lancet. Neurology|March 22, 2025
Paediatric neurology in Ukraine: a call for helpAlla Nechai, Oxana Nazar, Kevin Rostasy, et al.
Pageof 13