Understanding Lennox–Gastaut syndrome: insights from focal epilepsy patients with Lennox–Gastaut features
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
http://link.springer.com/article/10.1007/s00415-017-8535-7/fulltext.html
Reference31 articles.
1. Arzimanoglou A, French J, Blume WT et al (2009) Lennox–Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology. Lancet Neurol 8:82–93
2. Camfield P, Camfield C (2002) Epileptic syndromes in childhood: clinical features, outcomes, and treatment. Epilepsia 43(Suppl. 3):27–32
3. Bourgeois BF, Douglass LM, Sankar R (2014) Lennox–Gastaut syndrome: a consensus approach to differential diagnosis. Epilepsia 55(Suppl. 4):4–9
4. Gastaut H, Roger J, Soulayrol R et al (1966) Childhood epileptic encephalopathy with diffuse slow spike-waves (otherwise known as “petit mal variant”) or Lennox syndrome. Epilepsia 7:139–179
5. Markand ON (1977) Slow spike-wave activity in EEG and associated clinical features: often called ‘Lennox’ or “Lennox–Gastaut’ syndrome. Neurology 27:746–757
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