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M Zuberi

Showing results (51-60 of 170) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 30, 2001
Hashimoto's thyroiditis--a rare but treatable cause of encephalopathy in childrenO C Byrne, S M Zuberi, C A Madigan, et al.
Biochemistry|December 10, 1991
Identification of a ferryl intermediate of Escherichia coli cytochrome d terminal oxidase by resonance Raman spectroscopyM A Kahlow, T M Zuberi, R B Gennis, et al.
Archives of Disease in Childhood|September 15, 2005
Anoxic-epileptic seizures: observational study of epileptic seizures induced by syncopesI A Horrocks, A Nechay, J B P Stephenson, et al.
Brain : a Journal of Neurology|June 22, 2012
Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndromeA Brunklaus, R Ellis, E Reavey, et al.
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.
Applied Clinical Informatics|April 26, 2013
Using real-time alerts for clinical trials: Identifying potential study subjectsE Chow, M Zuberi, R Seto, 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.
Neurology|January 21, 2011
Genotype-phenotype associations in SCN1A-related epilepsiesS M Zuberi, A Brunklaus, R Birch, et al.
Pageof 17

Showing results (51-60 of 170) with videos related to

Sort By:
Pageof 17
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 30, 2001
Hashimoto's thyroiditis--a rare but treatable cause of encephalopathy in childrenO C Byrne, S M Zuberi, C A Madigan, et al.
Biochemistry|December 10, 1991
Identification of a ferryl intermediate of Escherichia coli cytochrome d terminal oxidase by resonance Raman spectroscopyM A Kahlow, T M Zuberi, R B Gennis, et al.
Archives of Disease in Childhood|September 15, 2005
Anoxic-epileptic seizures: observational study of epileptic seizures induced by syncopesI A Horrocks, A Nechay, J B P Stephenson, et al.
Brain : a Journal of Neurology|June 22, 2012
Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndromeA Brunklaus, R Ellis, E Reavey, et al.
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.
Applied Clinical Informatics|April 26, 2013
Using real-time alerts for clinical trials: Identifying potential study subjectsE Chow, M Zuberi, R Seto, 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.
Neurology|January 21, 2011
Genotype-phenotype associations in SCN1A-related epilepsiesS M Zuberi, A Brunklaus, R Birch, et al.
Pageof 17