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Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature.
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- Human Mutation, 2020, v. 41, n. 1, p. 69, doi. 10.1002/humu.23915
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Developmental and epilepsy spectrum of KCNB1 encephalopathy with long‐term outcome.
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- Epilepsia (Series 4), 2020, v. 61, n. 11, p. 2461, doi. 10.1111/epi.16679
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- Article
ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate.
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- Epilepsia (Series 4), 2016, v. 57, n. 7, p. 1069, doi. 10.1111/epi.13420
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- Article