Rima Nabbout
0000-0001-5877-4074
12 papers found
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Response: Do all individuals with Dravet syndrome have intellectual disability?
Which terms should be used to describe medications used in the treatment of seizure disorders? An ILAE position paper
Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox–Gastaut syndrome: Interim analysis of an open‐label extension study
Arterial Spin-Labeling Perfusion Imaging in the Early Stage of Sturge-Weber Syndrome
ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions
International League Against Epilepsy classification and definition of epilepsy syndromes with onset at a variable age: position statement by the ILAE Task Force on Nosology and Definitions
ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions
Methodology for classification and definition of epilepsy syndromes with list of syndromes: Report of the ILAE Task Force on Nosology and Definitions
International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions
Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature
Functional cortico-subcortical reorganization after complete hemispheric disconnection for intractable epilepsy
Gene mutations in paediatric epilepsies cause NMDA‐pathy, and phasic and tonic GABA‐pathy
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