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SCN1A Genetic Test for Dravet Syndrome (Severe Myoclonic Epilepsy of Infancy and its Clinical Subtypes) for use in the Diagnosis, Prognosis, Treatment and Management of Dravet Syndrome.
- Published in:
- PLoS Currents, 2013, p. 602, doi. 10.1371/currents.eogt.c553b83d745dd79bfb61eaf35e522b0b
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- Article
Do We All Know the Score?
- Published in:
- Child Abuse Review, 1998, v. 7, n. 5, p. 360, doi. 10.1002/(SICI)1099-0852(1998090)7:5<360::AID-CAR499>3.0.CO;2-L
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- Article
Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.
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- Brain: A Journal of Neurology, 2011, v. 134, n. 10, p. 2982, doi. 10.1093/brain/awr129
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- Article
The clinical utility of an SCN1A genetic diagnosis in infantile-onset epilepsy.
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- Developmental Medicine & Child Neurology, 2013, v. 55, n. 2, p. 154, doi. 10.1111/dmcn.12030
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- Article