Roberta Epifanio
Bosisio Parini, 23842, Italy
Last Updated: 09/26/2026
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Found 14 publications
SCN2A Pathogenic Variants and Epilepsy: Heterogeneous Clinical, Genetic and Diagnostic Features.
Journal: Brain sciences
Published: November 09, 2021
Lacosamide effectiveness and tolerability in patients with drug-resistant epilepsy and severe disability under polytherapy: Therapy optimization as emerging from an observational study.
Journal: Epilepsy & behavior : E&B
Published: November 08, 2021
Further delineation and long-term evolution of electroclinical phenotype in Mowat Wilson Syndrome. A longitudinal study in 40 individuals.
Journal: Epilepsy & behavior : E&B
Published: June 30, 2021
Novel epilepsy phenotype associated to a known SCN8A mutation.
Journal: Seizure
Published: December 17, 2018
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 07, 2017
Electrical status epilepticus during sleep in Mowat-Wilson syndrome.
Journal: Brain & development
Published: January 21, 2017
Partial deletion of DEPDC5 in a child with focal epilepsy.
Journal: Epilepsia open
Published: July 25, 2016
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 27, 2016
Late Post-traumatic Epilepsy in Children and Young Adults: Impropriety of Long-Term Antiepileptic Prophylaxis and Risks in Tapering.
Journal: Paediatric drugs
Published: February 26, 2016
Paroxysmal phenomena in severe disabled children with refractory seizures. From clinical to long-video-EEG processing data to re-examine suspect events.
Journal: Research in developmental disabilities
Published: December 19, 2013
Last Updated: 09/26/2026