Dravet syndrome—toward an optimal and disease-specific treatment
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s10309-021-00399-z.pdf
Reference49 articles.
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2. Heger K, Lund C, Larsen Burns M, et al (2020) A retrospective review of changes and challenges in the use of antiseizure medicines in Dravet syndrome in Norway. Epilepsia Open 5(3):432–441
3. Symonds JD, Zuberi SM, Stewart K et al (2019) Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort. Brain 1:2303–2318
4. Brunklaus A, Ellis R, Reavey E, et al (2012) Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome. Brain 135(Pt 8):2329–2336
5. Bayat A, Hjalgrim H, Moller RS (2015) The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: a population-based study from 2004 to 2009. Epilepsia 56(4):e36–e39
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