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Epilepsia, ISSN 0013-9580, 02/2016, Volume 57, Issue 2, pp. 182 - 193
Autism and epilepsy are two associated disorders that are highly prevalent, share common developmental origins, and demonstrate substantial heritability. In... 
Gamma‐aminobutyric acid | Epileptic encephalopathy | Epilepsy | Cortical interneuron | Autism spectrum disorder | Gamma-aminobutyric acid | RETT-SYNDROME | CLINICAL NEUROLOGY | CHILDREN | LANDAU-KLEFFNER | SEIZURES | DE-NOVO MUTATIONS | MOUSE MODEL | FRAGILE-X-SYNDROME | DRAVET-SYNDROME | SEVERE MYOCLONIC EPILEPSY | MICE | Landau-Kleffner Syndrome - physiopathology | Neural Inhibition | Spasms, Infantile - physiopathology | gamma-Aminobutyric Acid - metabolism | Humans | Autism Spectrum Disorder - complications | Child, Preschool | Infant | Aicardi Syndrome - genetics | Epilepsy - physiopathology | Spasms, Infantile - genetics | Cerebral Cortex - metabolism | Lennox Gastaut Syndrome - genetics | Lennox Gastaut Syndrome - psychology | Cerebral Cortex - physiopathology | Landau-Kleffner Syndrome - psychology | Epilepsy - genetics | Neurons - metabolism | Spasms, Infantile - complications | Child | Epilepsies, Myoclonic - genetics | Autism Spectrum Disorder - genetics | Epilepsy - psychology | Aicardi Syndrome - complications | Epilepsies, Myoclonic - physiopathology | Spasms, Infantile - psychology | Autism Spectrum Disorder - psychology | Landau-Kleffner Syndrome - genetics | Epilepsies, Myoclonic - complications | Epilepsy - complications | Landau-Kleffner Syndrome - complications | Aicardi Syndrome - psychology | Epilepsies, Myoclonic - psychology | Interneurons - metabolism | Aicardi Syndrome - physiopathology | Lennox Gastaut Syndrome - complications | Lennox Gastaut Syndrome - physiopathology | Autism Spectrum Disorder - physiopathology | GABA | Autism | Neurosciences
Journal Article
Canadian Journal of Neurological Sciences, ISSN 0317-1671, 06/2016, Volume 43, Issue 3, pp. S13 - S18
Journal Article
Journal Article
Epilepsy and Behavior, ISSN 1525-5050, 2016, Volume 64, Issue Pt A, pp. 69 - 74
Journal Article
Epilepsia, ISSN 0013-9580, 10/2018, Volume 59, Issue 10, pp. 1881 - 1888
Objective Lennox-Gastaut syndrome (LGS) is a drug-resistant, childhood onset electroclinical epilepsy syndrome with multiple seizure types and diagnostic... 
008 | phase 2 | childhood epilepsy | seizure frequency | fenfluramine | Lennox‐Gastaut syndrome | Lennox-Gastaut syndrome | ZX008 | DIAGNOSIS | CANNABIDIOL | DRAVET SYNDROME | STIRIPENTOL | CLINICAL NEUROLOGY | TRIAL | IN-VITRO | INHIBITION | SEIZURES | METABOLISM | SEROTONIN | Medical research | Epilepsy | Medicine, Experimental | Fenfluramine | Dosage and administration | Seizures (Medicine) | Drug resistance | Oral medication
Journal Article
Epilepsia, ISSN 0013-9580, 07/2012, Volume 53, Issue 7, pp. 1131 - 1139
Purpose:  Despite the development of new antiepileptic drugs, Dravet syndrome frequently remains therapy resistant and is a catastrophic epilepsy syndrome.... 
Fenfluramine | Orphan drugs | Severe myoclonic epilepsy in infancy | Dravet syndrome | SCN1A | DIAGNOSIS | TOPIRAMATE | STIRIPENTOL | CLINICAL NEUROLOGY | CHILD