Comprehensive care of children with Dravet syndrome
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2011.03011.x/fullpdf
Reference14 articles.
1. Neuropsychological Aspects of Severe Myoclonic Epilepsy in Infancy
2. Severe myoclonic epilepsy in infancy: toward an optimal treatment;Ceulemans;J Child Neurol,2004
3. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001
4. Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients;Depienne;J Med Genet,2009
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2. Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe;Epilepsia Open;2021-12-19
3. The impact of seizure frequency on quality of life in patients with Lennox-Gastaut syndrome or Dravet syndrome;Epilepsy & Behavior;2021-10
4. Functional communication training and delay to reinforcement for the treatment of elopement in a boy with Dravet syndrome;Behavioral Interventions;2021-06-25
5. Cognitive, behavioral, and social functioning in children and adults with Dravet syndrome;Epilepsy & Behavior;2020-11
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