Roberta Solazzi
10PUBLICATIONS
72CO-AUTHORS
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Publications (10)
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|Nov 24, 2025
Compound Heterozygous PNKP Variants Causing Developmental and Epileptic Encephalopathy with Severe Microcephaly: Natural History of Two New Cases and Literature Review.Francesca Ragona, Giuliana Messina, Stefania Magri
|Oct 25, 2025
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiology.Simona Balestrini, Ilaria Galli, Maria Luisa Ricci
|Oct 24, 2025
Genetic complexity in pediatric onset epilepsy-movement disorder syndromes: Insights from a cohort of 97 subjects.Davide Caputo, Roberta Solazzi, Barbara Castellotti
|Dec 24, 2024
CLN6-related continuum phenotype caused by aberrant splicing.Federica Invernizzi, Barbara Castellotti, Chiara Reale
|Aug 31, 2024
Next-generation sequencing in pediatric-onset epilepsies: Analysis with target panels and personalized therapeutic approach.Barbara Castellotti, Francesca Ragona, Elena Freri
|Mar 16, 2024
Clinical and molecular characterization of patients with YWHAG-related epilepsy.Valentina Cetica, Tiziana Pisano, Gaetan Lesca
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Frequent Collaborators
7 joint publications
Laura Canafoglia
6 joint publications
Barbara Castellotti
5 joint publications
Tiziana Granata
4 joint publications
Jacopo Cosimo DiFrancesco
3 joint publications
Elena Freri
3 joint publications
Giuliana Messina
3 joint publications
Francesca Ragona
2 joint publications
Cinzia Gellera
2 joint publications
Tommaso Lo Barco
2 joint publications
Francesca Darra
