Maria Virginia Soldovieri
10PUBLICATIONS
38CO-AUTHORS
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Publications (10)
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|Feb 21, 2025
Fluoxetine Treatment in Epilepsy of Infancy with Migrating Focal Seizures Due to KCNT1 Variants: An Open Label Study.Marina Trivisano, Ilaria Mosca, Licia Salimbene
|Nov 27, 2024
Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2-developmental encephalopathy.Mario Nappi, Giulio Alberini, Alessandro Berselli
|Nov 15, 2023
De novo variants in KCNA3 cause developmental and epileptic encephalopathy.Maria Virginia Soldovieri, Paolo Ambrosino, Ilaria Mosca
|May 19, 2023
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine.Paolo Ambrosino, Francesca Ragona, Ilaria Mosca
|Apr 16, 2023
KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological Properties.Maria Cristina Cioclu, Ilaria Mosca, Paolo Ambrosino
|Jun 22, 2022
The long and winding road to personalized medicine in KCNMA1-linked channelopathies revealed by novel variants associated with the Liang-Wang syndrome.Maria Virginia Soldovieri, Maurizio Taglialatela
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Frequent Collaborators
7 joint publications
Maurizio Taglialatela
3 joint publications
Francesco Miceli
2 joint publications
Vincenzo Barrese
1 joint publications
Beth Kline-Fath
1 joint publications
Erika Di Zazzo
1 joint publications
Gianluca Paventi
1 joint publications
Fabio Arturo Iannotti
1 joint publications
Cristina Franco
1 joint publications
Renzo Guerrini
1 joint publications
Elena Cellini
