Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome
Author:
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/135/8/2329/864709/aws151.pdf
Reference44 articles.
1. De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study
2. Comorbidities and predictors of health-related quality of life in Dravet syndrome
3. Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology
4. Severe Myoclonic Epilepsy in Infancy: Toward an Optimal Treatment
5. Unusual consequences of status epilepticus in Dravet syndrome
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