Borderline Dravet syndrome: A useful diagnostic category?
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2011.02995.x/fullpdf
Reference11 articles.
1. Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females;Depienne;PLoS Genet,2009
2. Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures;Fujiwara;Brain,2003
3. Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB);Fukuma;Epilepsia,2004
4. Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene;Guerrini;Epilepsia,2010
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2. The Promising Epigenetic Regulators for Refractory Epilepsy: An Adventurous Road Ahead;NeuroMolecular Medicine;2022-09-24
3. Phenotypic and Genotypic Characteristics of SCN1A Associated Seizure Diseases;Frontiers in Molecular Neuroscience;2022-04-28
4. Genetic Landscape of <b><i>SCN1A</i></b> Variants in a Turkish Cohort with GEFS+ Spectrum and Dravet Syndrome;Molecular Syndromology;2022-02-22
5. Heart rate variability alterations in Dravet Syndrome: The role of status epilepticus and a possible association with mortality risk;Seizure;2022-01
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