Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Roberta Solazzi

Showing results (11-20 of 33) with videos related to

Pageof 4
Sort By:
Epileptic Disorders : International Epilepsy Journal with Videotape|May 17, 2023
Gelastic seizures and "smiling spasms": A peculiar ictal patternTommaso Lo Barco, Laura Corona, Roberta Solazzi, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 14, 2021
Paroxysmal tonic upgaze in a child with SCN8A-related encephalopathyRoberta Solazzi, Barbara Castellotti, Laura Canafoglia, et al.
Neurosci|November 24, 2025
Compound Heterozygous <i>PNKP</i> Variants Causing Developmental and Epileptic Encephalopathy with Severe Microcephaly: Natural History of Two New Cases and Literature ReviewFrancesca Ragona, Giuliana Messina, Stefania Magri, et al.
Seizure|April 25, 2021
Severe epilepsy in CNTNAP2-related Pitt-Hopkins-like syndrome successfully treated with stiripentolElena Freri, Barbara Castellotti, Laura Canafoglia, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 21, 2024
Cortical Myoclonus and Complex Paroxysmal Dyskinesias in a Patient with NAA15 VariantElena Freri, Laura Canafoglia, Claudia Ciaccio, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 14, 2021
CDKL5 deficiency disorder in males: Five new variants and review of the literatureBarbara Siri, Costanza Varesio, Elena Freri, et al.
Epilepsia Open|August 31, 2024
Next-generation sequencing in pediatric-onset epilepsies: Analysis with target panels and personalized therapeutic approachBarbara Castellotti, Francesca Ragona, Elena Freri, et al.
Seizure|October 2, 2020
SCN8A splicing mutation causing skipping of the exon 15 associated with intellectual disability and cortical myoclonusLaura Canafoglia, Silvana Franceschetti, Tiziana Granata, et al.
Frontiers in Cellular Neuroscience|February 10, 2025
Pharmacological approaches in drug-resistant pediatric epilepsies caused by pathogenic variants in potassium channel genesIlaria Filareto, Ilaria Mosca, Elena Freri, et al.
Journal of Neurology|March 22, 2019
Screening of SLC2A1 in a large cohort of patients suspected for Glut1 deficiency syndrome: identification of novel variants and associated phenotypesBarbara Castellotti, Francesca Ragona, Elena Freri, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Epileptic Disorders : International Epilepsy Journal with Videotape|May 17, 2023
Gelastic seizures and "smiling spasms": A peculiar ictal patternTommaso Lo Barco, Laura Corona, Roberta Solazzi, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 14, 2021
Paroxysmal tonic upgaze in a child with SCN8A-related encephalopathyRoberta Solazzi, Barbara Castellotti, Laura Canafoglia, et al.
Neurosci|November 24, 2025
Compound Heterozygous <i>PNKP</i> Variants Causing Developmental and Epileptic Encephalopathy with Severe Microcephaly: Natural History of Two New Cases and Literature ReviewFrancesca Ragona, Giuliana Messina, Stefania Magri, et al.
Seizure|April 25, 2021
Severe epilepsy in CNTNAP2-related Pitt-Hopkins-like syndrome successfully treated with stiripentolElena Freri, Barbara Castellotti, Laura Canafoglia, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 21, 2024
Cortical Myoclonus and Complex Paroxysmal Dyskinesias in a Patient with NAA15 VariantElena Freri, Laura Canafoglia, Claudia Ciaccio, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 14, 2021
CDKL5 deficiency disorder in males: Five new variants and review of the literatureBarbara Siri, Costanza Varesio, Elena Freri, et al.
Epilepsia Open|August 31, 2024
Next-generation sequencing in pediatric-onset epilepsies: Analysis with target panels and personalized therapeutic approachBarbara Castellotti, Francesca Ragona, Elena Freri, et al.
Seizure|October 2, 2020
SCN8A splicing mutation causing skipping of the exon 15 associated with intellectual disability and cortical myoclonusLaura Canafoglia, Silvana Franceschetti, Tiziana Granata, et al.
Frontiers in Cellular Neuroscience|February 10, 2025
Pharmacological approaches in drug-resistant pediatric epilepsies caused by pathogenic variants in potassium channel genesIlaria Filareto, Ilaria Mosca, Elena Freri, et al.
Journal of Neurology|March 22, 2019
Screening of SLC2A1 in a large cohort of patients suspected for Glut1 deficiency syndrome: identification of novel variants and associated phenotypesBarbara Castellotti, Francesca Ragona, Elena Freri, et al.
Pageof 4