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Roberta Solazzi

Showing results (21-30 of 33) with videos related to

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Frontiers in Cellular Neuroscience|April 22, 2024
Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with <i>KCNT1</i>-related drug-resistant focal epilepsyIlaria Mosca, Elena Freri, Paolo Ambrosino, et al.
Epilepsia|October 24, 2025
Genetic complexity in pediatric onset epilepsy-movement disorder syndromes: Insights from a cohort of 97 subjectsDavide Caputo, Roberta Solazzi, Barbara Castellotti, et al.
Epilepsia|May 19, 2023
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetinePaolo Ambrosino, Francesca Ragona, Ilaria Mosca, et al.
Epilepsia Open|December 24, 2024
CLN6-related continuum phenotype caused by aberrant splicingFederica Invernizzi, Barbara Castellotti, Chiara Reale, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 27, 2021
SYNGAP1-DEE: A visual sensitive epilepsyTommaso Lo Barco, Anna Kaminska, Roberta Solazzi, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 10, 2023
CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndromeNicola Specchio, Marina Trivisano, Matteo Lenge, et al.
Pharmacological Research|September 17, 2020
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathyMaria Virginia Soldovieri, Elena Freri, Paolo Ambrosino, et al.
Epilepsia|September 25, 2023
A novel de novo HCN2 loss-of-function variant causing developmental and epileptic encephalopathy treated with a ketogenic dietJacopo C DiFrancesco, Francesca Ragona, Carmen Murano, et al.
Epilepsy Research|April 16, 2019
HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literatureJacopo C DiFrancesco, Barbara Castellotti, Raffaella Milanesi, et al.
Epilepsia|October 25, 2025
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiologySimona Balestrini, Ilaria Galli, Maria Luisa Ricci, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Frontiers in Cellular Neuroscience|April 22, 2024
Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with <i>KCNT1</i>-related drug-resistant focal epilepsyIlaria Mosca, Elena Freri, Paolo Ambrosino, et al.
Epilepsia|October 24, 2025
Genetic complexity in pediatric onset epilepsy-movement disorder syndromes: Insights from a cohort of 97 subjectsDavide Caputo, Roberta Solazzi, Barbara Castellotti, et al.
Epilepsia|May 19, 2023
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetinePaolo Ambrosino, Francesca Ragona, Ilaria Mosca, et al.
Epilepsia Open|December 24, 2024
CLN6-related continuum phenotype caused by aberrant splicingFederica Invernizzi, Barbara Castellotti, Chiara Reale, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 27, 2021
SYNGAP1-DEE: A visual sensitive epilepsyTommaso Lo Barco, Anna Kaminska, Roberta Solazzi, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 10, 2023
CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndromeNicola Specchio, Marina Trivisano, Matteo Lenge, et al.
Pharmacological Research|September 17, 2020
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathyMaria Virginia Soldovieri, Elena Freri, Paolo Ambrosino, et al.
Epilepsia|September 25, 2023
A novel de novo HCN2 loss-of-function variant causing developmental and epileptic encephalopathy treated with a ketogenic dietJacopo C DiFrancesco, Francesca Ragona, Carmen Murano, et al.
Epilepsy Research|April 16, 2019
HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literatureJacopo C DiFrancesco, Barbara Castellotti, Raffaella Milanesi, et al.
Epilepsia|October 25, 2025
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiologySimona Balestrini, Ilaria Galli, Maria Luisa Ricci, et al.
Pageof 4