Dravet syndrome: Seizure control and gait in adults with different SCN1A mutations
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2012.03583.x/fullpdf
Reference21 articles.
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2. Dravet syndrome and deep brain stimulation: seizure control after 10 years of treatment;Andrade;Epilepsia,2010
3. From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels;Catterall;Neuron,2000
4. A “minimal” sodium channel construct consisting of ligated S5-P-S6 segments forms a toxin-activatable ionophore;Chen;J Biol Chem,2002
5. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001
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1. Clinical and Genetic Features of Dravet Syndrome: A Prime Example of the Role of Precision Medicine in Genetic Epilepsy;International Journal of Molecular Sciences;2023-12-19
2. Epileptic seizures worsen the gait and motor abnormalities in adult patients with Dravet syndrome (with a case report and literature review);Epilepsia Open;2023-10-06
3. Features of epileptic encephalopathy caused by SCN1A mutation;INTERNATIONAL NEUROLOGICAL JOURNAL;2023-09-08
4. Functional mobility in children and young adults with Dravet syndrome;Developmental Medicine & Child Neurology;2023-02-28
5. Sleep slow-wave oscillations trigger seizures in a genetic epilepsy model of Dravet syndrome;Brain Communications;2022-12-17
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