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SCN2A Pathogenic Variants and Epilepsy: Heterogeneous Clinical, Genetic and Diagnostic Features.
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- Brain Sciences (2076-3425), 2022, v. 12, n. 1, p. 18, doi. 10.3390/brainsci12010018
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- Article
Expanding Phenotype of Poirier–Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients.
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- Genes, 2022, v. 13, n. 2, p. 276, doi. 10.3390/genes13020276
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- Article
Late Post-traumatic Epilepsy in Children and Young Adults: Impropriety of Long-Term Antiepileptic Prophylaxis and Risks in Tapering.
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- Pediatric Drugs, 2016, v. 18, n. 3, p. 235, doi. 10.1007/s40272-016-0167-3
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- Article
Visual Function in Infants with West Syndrome: Correlation with EEG Patterns.
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- Epilepsia (Series 4), 2004, v. 45, n. 7, p. 781, doi. 10.1111/j.0013-9580.2004.41403.x
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- Article
Randò et al. reply.
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- Developmental Medicine & Child Neurology, 2006, v. 48, n. 11, p. 942, doi. 10.1017/S0012162206222059
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- Article
Cognitive competence at the onset of West syndrome: correlation with EEG patterns and visual function.
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- Developmental Medicine & Child Neurology, 2005, v. 47, n. 11, p. 760, doi. 10.1017/S0012162205001593
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- Article
Partial deletion of DEPDC5 in a child with focal epilepsy.
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- Epilepsia Open, 2016, v. 1, n. 3/4, p. 140, doi. 10.1002/epi4.12012
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- Article
Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 2, p. 273, doi. 10.1002/ajmg.a.35717
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- Article
Electroclinical pattern in MECP2 duplication syndrome: Eight new reported cases and review of literature.
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- Epilepsia (Series 4), 2012, v. 53, n. 7, p. 1146, doi. 10.1111/j.1528-1167.2012.03501.x
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- Article