Angela De Dominicis

10PUBLICATIONS
126CO-AUTHORS
PharmacogenomicsEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesOther European languagesGene expression (incl. microarray and other genome-wide approaches)
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Publications (10)

|Sep 10, 2026
Efficacy of stiripentol, fenfluramine, and their combination on clinical outcomes in Dravet syndrome: A preliminary report.

|Mar 12, 2026
Early Clinical and EEG Association of Genotype and Outcome in Genetic Epilepsies: A Cohort Study and Hierarchical Clustering Analysis.

Angela De Dominicis, Mattia Mercier, Giusy Carfi Pavia

|Feb 27, 2026
Circulating microRNAs as biomarkers in pediatric epilepsy: A longitudinal cohort study.

Licia Salimbene, Mattia Mercier, Valentina Spedaletti

|Feb 05, 2026
Mechanisms of SCN2A loss of function do not predict presence or phenotype of epilepsy.

Marsha Tan, Beatrice Southby Goad, Meagan Allen

|Jan 28, 2026
Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants.

Sebastian Ortiz, Leonardo Affronte, Chiara Bagliani

|Oct 25, 2025
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiology.

Simona Balestrini, Ilaria Galli, Maria Luisa Ricci

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Frequent Collaborators

10 joint publications

Nicola Specchio

8 joint publications

Marina Trivisano

4 joint publications

Costanza Calabrese

3 joint publications

Mattia Mercier