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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.Handbook of Clinical Neurology|April 30, 2013
Chromosome disorders associated with epilepsySameer M ZuberiEpilepsia|May 20, 2014
Dravet syndrome--from epileptic encephalopathy to channelopathyAndreas Brunklaus, Sameer M ZuberiNeuropharmacology|August 1, 2017
WITHDRAWN: Genetics update: Monogenetics, polygene disorders and the quest for modifying genesJoseph D Symonds, Sameer M ZuberiNeuropharmacology|October 18, 2017
Genetics update: Monogenetics, polygene disorders and the quest for modifying genesJoseph D Symonds, Sameer M ZuberiJornal De Pediatria|September 11, 2015
Update on diagnosis and management of childhood epilepsiesSameer M Zuberi, Joseph D SymondsEpilepsy Research|August 15, 2006
Developmental outcome in benign myoclonic epilepsy in infancy and reflex myoclonic epilepsy in infancy: a literature review and six new casesSameer M Zuberi, Mary E O'ReganNeurology and Therapy|February 11, 2016
Treatment of Adults with Lennox-Gastaut Syndrome: Further Analysis of Efficacy and Safety/Tolerability of RufinamideRob McMurray, Pasquale StrianoExpert Opinion on Investigational Drugs|November 27, 2009
New and investigational antiepileptic drugsPasquale Striano, Salvatore StrianoDrugs of Today (Barcelona, Spain : 1998)|June 13, 2008
Gabapentin: a Ca2+ channel alpha 2-delta ligand far beyond epilepsy therapyPasquale Striano, Salvatore StrianoPageof 77