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Sameer M Zuberi

Showing results (71-80 of 123) with videos related to

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The Lancet. Neurology|May 23, 2006
De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective studySamuel F Berkovic, Louise Harkin, Jacinta M McMahon, et al.
The New England Journal of Medicine|May 17, 2018
Effect of Cannabidiol on Drop Seizures in the Lennox-Gastaut SyndromeOrrin Devinsky, Anup D Patel, J Helen Cross, et al.
Human Mutation|November 30, 2019
SCN1A variants from bench to bedside-improved clinical prediction from functional characterizationAndreas Brunklaus, Stephanie Schorge, Alexander D Smith, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 3, 2024
CSF-profile and hypocretin levels in children with narcolepsy type 1 and 2Maike Josler, Ines El Naggar, Annikki Bertolini, et al.
Epilepsia|April 19, 2003
Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsyAilsa McLellan, Hilary A Phillips, Christopher Rittey, et al.
Journal of Medical Genetics|October 6, 2018
PEHO syndrome: the endpoint of different genetic epilepsiesManali Chitre, Michael S Nahorski, Kaitlin Stouffer, et al.
Epilepsia|March 10, 2017
Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and TerminologyRobert S Fisher, J Helen Cross, Jacqueline A French, et al.
Pediatrics|February 5, 2008
Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardationAgatino Battaglia, H Eugene Hoyme, Bruno Dallapiccola, et al.
Neurology. Genetics|April 27, 2026
Elicited Repetitive Daily Blindness Associated With Gain-of-Function <i>SCN1A</i> Variants and Responsiveness to Sodium Channel BlockersSandrine Cestèle, Alexander James Harper, Sebastian Marra, et al.
Epilepsia|February 1, 2021
The ILAE classification of seizures and the epilepsies: Modification for seizures in the neonate. Position paper by the ILAE Task Force on Neonatal SeizuresRonit M Pressler, Maria Roberta Cilio, Eli M Mizrahi, et al.
Pageof 13

Showing results (71-80 of 123) with videos related to

Sort By:
Pageof 13
The Lancet. Neurology|May 23, 2006
De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective studySamuel F Berkovic, Louise Harkin, Jacinta M McMahon, et al.
The New England Journal of Medicine|May 17, 2018
Effect of Cannabidiol on Drop Seizures in the Lennox-Gastaut SyndromeOrrin Devinsky, Anup D Patel, J Helen Cross, et al.
Human Mutation|November 30, 2019
SCN1A variants from bench to bedside-improved clinical prediction from functional characterizationAndreas Brunklaus, Stephanie Schorge, Alexander D Smith, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 3, 2024
CSF-profile and hypocretin levels in children with narcolepsy type 1 and 2Maike Josler, Ines El Naggar, Annikki Bertolini, et al.
Epilepsia|April 19, 2003
Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsyAilsa McLellan, Hilary A Phillips, Christopher Rittey, et al.
Journal of Medical Genetics|October 6, 2018
PEHO syndrome: the endpoint of different genetic epilepsiesManali Chitre, Michael S Nahorski, Kaitlin Stouffer, et al.
Epilepsia|March 10, 2017
Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and TerminologyRobert S Fisher, J Helen Cross, Jacqueline A French, et al.
Pediatrics|February 5, 2008
Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardationAgatino Battaglia, H Eugene Hoyme, Bruno Dallapiccola, et al.
Neurology. Genetics|April 27, 2026
Elicited Repetitive Daily Blindness Associated With Gain-of-Function <i>SCN1A</i> Variants and Responsiveness to Sodium Channel BlockersSandrine Cestèle, Alexander James Harper, Sebastian Marra, et al.
Epilepsia|February 1, 2021
The ILAE classification of seizures and the epilepsies: Modification for seizures in the neonate. Position paper by the ILAE Task Force on Neonatal SeizuresRonit M Pressler, Maria Roberta Cilio, Eli M Mizrahi, et al.
Pageof 13