Next‐generation sequencing in pediatric‐onset epilepsies: Analysis with target panels and personalized therapeutic approach
The analysis of patients with pediatric-onset epilepsy using advanced technologies for the screening of all the implicated genes allows the identification of the cause of diseases in an ever-increasing number of cases. Understanding the pathogenic mechanisms could, in some cases, guide the selection and optimization of appropriate treatment approaches for patients.
Authors
- Roberta Solazzi (ORCID: https://orcid.org/0000-0001-6657-3328)
- Francesca Ragona (ORCID: https://orcid.org/0000-0003-1399-8271)
- Roberto Previtali (ORCID: https://orcid.org/0000-0002-3295-0655)
- Jacopo Cosimo DiFrancesco (ORCID: https://orcid.org/0000-0002-4102-1188)
- Laura Canafoglia (ORCID: https://orcid.org/0000-0002-5385-761X)
- Franco Taroni (ORCID: https://orcid.org/0000-0002-2269-4504)
- Silvana Franceschetti (ORCID: https://orcid.org/0000-0002-1921-6755)
- Giuliana Messina (ORCID: https://orcid.org/0000-0002-5889-2342)
- Tiziana Granata (ORCID: https://orcid.org/0000-0002-0170-6836)
- Barbara Castellotti (ORCID: https://orcid.org/0000-0002-9098-3041)
- Elena Freri (ORCID: https://orcid.org/0000-0002-2293-8687)
- Cinzia Gellera (ORCID: https://orcid.org/0000-0002-3582-665X)
- Stefania Magri
Institutions
- University of Milan (IT)
- Azienda Ospedaliera San Gerardo (IT)
- Istituti di Ricovero e Cura a Carattere Scientifico (IT)
- Fondazione IRCCS Istituto Neurologico Carlo Besta (IT)
Publication Details
- Journal
- Epilepsia Open
- Published
- 2024-08-31
- DOI
- https://doi.org/10.1002/epi4.13039
- Citations
- 9
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 4.95
Funders
- Ministero della Salute