Antonella Boni

Bologna, Italy

Last Updated: 09/26/2026

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Found 25 publications

Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.

Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.

Journal: American journal of human genetics

Published: March 11, 2026

The impact of vagus nerve stimulation on the most disabling seizures: A retrospective study in adults with drug-resistant epilepsy.

The impact of vagus nerve stimulation on the most disabling seizures: A retrospective study in adults with drug-resistant epilepsy.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: October 06, 2025

Efficacy and Safety of Pulse Intravenous Methylprednisolone in Pediatric Epileptic Encephalopathies: Timing and Networks Consideration.

Efficacy and Safety of Pulse Intravenous Methylprednisolone in Pediatric Epileptic Encephalopathies: Timing and Networks Consideration.

Journal: Journal of clinical medicine

Published: March 05, 2024

Tuberous sclerosis complex in adulthood: focus on epilepsy prognosis.

Tuberous sclerosis complex in adulthood: focus on epilepsy prognosis.

Journal: Epilepsy & behavior : E&B

Published: November 04, 2023

A Male Child with Infantile Epilepsy due to a Mosaic Missense Variant of PCDH19.

A Male Child with Infantile Epilepsy due to a Mosaic Missense Variant of PCDH19.

Journal: Molecular syndromology

Published: May 04, 2023

Brivaracetam add-on treatment in pediatric patients with severe drug-resistant epilepsy: Italian real-world evidence.

Brivaracetam add-on treatment in pediatric patients with severe drug-resistant epilepsy: Italian real-world evidence.

Journal: Seizure

Published: January 12, 2022

Epilepsy Course and Developmental Trajectories in STXBP1-DEE.

Epilepsy Course and Developmental Trajectories in STXBP1-DEE.

Journal: Neurology. Genetics

Published: August 22, 2021

Further delineation and long-term evolution of electroclinical phenotype in Mowat Wilson Syndrome. A longitudinal study in 40 individuals.

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

Early vagus nerve stimulator implantation as a main predictor of positive outcome in pediatric patients with epileptic encephalopathy.

Early vagus nerve stimulator implantation as a main predictor of positive outcome in pediatric patients with epileptic encephalopathy.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: June 29, 2021

Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox-Gastaut Syndrome.

Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox-Gastaut Syndrome.

Journal: Frontiers in neurology

Published: February 26, 2021

In vitro and in vivo effects of Ambroxol chaperone therapy in two Italian patients affected by neuronopathic Gaucher disease and epilepsy.

In vitro and in vivo effects of Ambroxol chaperone therapy in two Italian patients affected by neuronopathic Gaucher disease and epilepsy.

Journal: Molecular genetics and metabolism reports

Published: October 16, 2020

A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies.

A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies.

Journal: Epilepsia open

Published: June 09, 2020

Showing 1-12 of 25

Last Updated: 09/26/2026