Neuropsychological Findings: Myoclonic Astatic Epilepsy (MAE) and Lennox-Gastaut Syndrome (LGS)
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2006.00691.x/fullpdf
Reference10 articles.
1. Treatment and Long-Term Prognosis of Myoclonic-Astatic Epilepsy of Early Childhood
2. Different Neurophysiologic Patterns of Myoclonus Characterize Lennox-Gastaut Syndrome and Myoclonic Astatic Epilepsy
3. Epileptic Encephalopathies with Myoclonic Seizures in Infants and Children (Severe Myoclonic Epilepsy and Myoclonic-Astatic Epilepsy)
4. Delineation of cryptogenic Lennox–Gastaut syndrome and myoclonic astatic epilepsy using multiple correspondence analysis
5. A Proposed Diagnostic Scheme for People with Epileptic Seizures and with Epilepsy: Report of the ILAE Task Force on Classification and Terminology
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1. Long‐term outcomes and adaptive behavior in adult patients with Lennox–Gastaut syndrome;Epilepsia Open;2024-08-07
2. Structural brain abnormalities in epilepsy with myoclonic atonic seizures;Epilepsy Research;2021-11
3. Cognitive, adaptive, and behavioral effects of adjunctive rufinamide in Lennox–Gastaut syndrome: A prospective observational clinical study;Epilepsy & Behavior;2020-11
4. Childhood and Adolescent Epileptic Syndromes;Clinical Child Neurology;2020
5. Usefulness of preschool and school versions of the Behavioral Rating Inventory of Executive Functions in the evaluation of the daily life executive function in myoclonic–atonic epilepsy;Epilepsy & Behavior;2019-10
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