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Angelo Russo

Showing results (81-90 of 88) with videos related to

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Epilepsia Open|March 20, 2023
A registry for Dravet syndrome: The Italian experienceSimona Balestrini, Viola Doccini, Sabrina Giometto, et al.
Epilepsia|February 3, 2023
Perampanel as precision therapy in rare genetic epilepsiesAndreea Nissenkorn, Gerhard Kluger, Susanne Schubert-Bast, et al.
Seizure|June 23, 2020
Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlationsAndrea Accogli, Mariasavina Severino, Antonella Riva, et al.
Neurology. Genetics|March 4, 2021
Genotype-phenotype correlations in patients with de novo <i>KCNQ2</i> pathogenic variantsFederica Malerba, Giulio Alberini, Ganna Balagura, et al.
Epilepsia|October 29, 2025
Lennox-Gastaut syndrome unveiled: Advancing diagnosis, therapies, and advocacy-insights from the Genoa International WorkshopAntonella Riva, Gianluca D'Onofrio, Elisabetta Amadori, et al.
Neurology. Genetics|June 3, 2022
Epilepsy Course and Developmental Trajectories in <i>STXBP1</i>-DEEGanna Balagura, Julie Xian, Antonella Riva, et al.
Neurology|July 22, 2025
Development and Adaptive Function in Individuals With <i>SCN2A</i>-Related DisordersBeatrice Southby Goad, Jill Rodda, Meagan Allen, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
The natural history of CDKL5 deficiency disorder into adulthoodAngel Aledo-Serrano, David Lewis-Smith, Helen Leonard, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
Epilepsia Open|March 20, 2023
A registry for Dravet syndrome: The Italian experienceSimona Balestrini, Viola Doccini, Sabrina Giometto, et al.
Epilepsia|February 3, 2023
Perampanel as precision therapy in rare genetic epilepsiesAndreea Nissenkorn, Gerhard Kluger, Susanne Schubert-Bast, et al.
Seizure|June 23, 2020
Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlationsAndrea Accogli, Mariasavina Severino, Antonella Riva, et al.
Neurology. Genetics|March 4, 2021
Genotype-phenotype correlations in patients with de novo <i>KCNQ2</i> pathogenic variantsFederica Malerba, Giulio Alberini, Ganna Balagura, et al.
Epilepsia|October 29, 2025
Lennox-Gastaut syndrome unveiled: Advancing diagnosis, therapies, and advocacy-insights from the Genoa International WorkshopAntonella Riva, Gianluca D'Onofrio, Elisabetta Amadori, et al.
Neurology. Genetics|June 3, 2022
Epilepsy Course and Developmental Trajectories in <i>STXBP1</i>-DEEGanna Balagura, Julie Xian, Antonella Riva, et al.
Neurology|July 22, 2025
Development and Adaptive Function in Individuals With <i>SCN2A</i>-Related DisordersBeatrice Southby Goad, Jill Rodda, Meagan Allen, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
The natural history of CDKL5 deficiency disorder into adulthoodAngel Aledo-Serrano, David Lewis-Smith, Helen Leonard, et al.
Pageof 9