Roberto Previtali

9PUBLICATIONS
66CO-AUTHORS
NeurogeneticsMajor global burdens of diseaseInfant and child healthEpigenetics (incl. genome methylation and epigenomics)
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Publications (9)

|Jan 21, 2026
GLUT1 deficiency syndrome in adulthood: lost in diagnosis.

Roberto Previtali, Lara Adami, Chiara Benvenuto

|Jan 15, 2025
Cenobamate as add-on treatment for SCN8A developmental and epileptic encephalopathy.

Cathrine E Gjerulfsen, Madeleine J Oudin, Francesca Furia

|Oct 28, 2024
Quantitative EEG biomarkers for STXBP1-related disorders.

Alberto Cossu, Francesca Furia, Jacopo Proietti

|Sep 10, 2024
Long-term health outcome and quality of life in children with multisystem inflammatory syndrome: findings from multidisciplinary follow-up at an Italian tertiary-care paediatric hospital.

Enza D'Auria, Stefania Maria Bova, Andrea Riccardo Dallapiccola

|Aug 31, 2024
Next-generation sequencing in pediatric-onset epilepsies: Analysis with target panels and personalized therapeutic approach.

Barbara Castellotti, Francesca Ragona, Elena Freri

|Sep 25, 2023
A novel de novo HCN2 loss-of-function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet.

Jacopo C DiFrancesco, Francesca Ragona, Carmen Murano

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Frequent Collaborators

4 joint publications

Pierangelo Veggiotti

3 joint publications

Rikke S Møller

3 joint publications

Guido Rubboli

3 joint publications

Francesca Furia