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Alessandro Orsini

Showing results (81-90 of 110) with videos related to

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Brain Communications|June 26, 2023
Variation in prognosis and treatment outcome in juvenile myoclonic epilepsy: a Biology of Juvenile Myoclonic Epilepsy Consortium proposal for a practical definition and stratified medicine classificationsGuido Rubboli, Christoph P Beier, Kaja K Selmer, et al.
Frontiers in Neurology|June 27, 2022
The Clinical Impact of Methotrexate-Induced Stroke-Like Neurotoxicity in Paediatric Departments: An Italian Multi-Centre Case-SeriesAndrea Santangelo, Emanuele Bartolini, Giulia Nuzzi, et al.
Epilepsia|March 31, 2023
Long-term effectiveness of add-on perampanel in patients with Lennox-Gastaut syndrome: A multicenter retrospective studySara Matricardi, Elisabetta Cesaroni, Paolo Bonanni, et al.
Molecular Genetics and Metabolism|March 23, 2026
Efficacy of JAK1/2 inhibitors in AGS genes-related interferonopathies: A multicenter retrospective observational study with treated vs untreated comparisonGemma Marinella, Ylenia Vaia, Davide Politano, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 12, 2020
Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patientsGanna Balagura, Antonella Riva, Francesca Marchese, et al.
Annals of Clinical and Translational Neurology|December 2, 2020
Trait impulsivity in Juvenile Myoclonic EpilepsyAmy Shakeshaft, Naim Panjwani, Robert McDowall, et al.
Scientific Reports|February 22, 2022
Sex-specific disease modifiers in juvenile myoclonic epilepsyAmy Shakeshaft, Naim Panjwani, Amber Collingwood, et al.
Pediatrics|November 20, 2025
Evaluation, Diagnosis, and Treatment of Sydenham Chorea: Consensus GuidelinesTerrence Thomas, Michael Eyre, Emanuela Ferrarin, et al.
Orphanet Journal of Rare Diseases|March 8, 2024
Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 childrenAnna Fetta, Francesco Toni, Ilaria Pettenuzzo, et al.
Journal of the Neurological Sciences|March 27, 2021
Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlationsAntonella Riva, Alessandro Orsini, Marcello Scala, et al.
Pageof 11

Showing results (81-90 of 110) with videos related to

Sort By:
Pageof 11
Brain Communications|June 26, 2023
Variation in prognosis and treatment outcome in juvenile myoclonic epilepsy: a Biology of Juvenile Myoclonic Epilepsy Consortium proposal for a practical definition and stratified medicine classificationsGuido Rubboli, Christoph P Beier, Kaja K Selmer, et al.
Frontiers in Neurology|June 27, 2022
The Clinical Impact of Methotrexate-Induced Stroke-Like Neurotoxicity in Paediatric Departments: An Italian Multi-Centre Case-SeriesAndrea Santangelo, Emanuele Bartolini, Giulia Nuzzi, et al.
Epilepsia|March 31, 2023
Long-term effectiveness of add-on perampanel in patients with Lennox-Gastaut syndrome: A multicenter retrospective studySara Matricardi, Elisabetta Cesaroni, Paolo Bonanni, et al.
Molecular Genetics and Metabolism|March 23, 2026
Efficacy of JAK1/2 inhibitors in AGS genes-related interferonopathies: A multicenter retrospective observational study with treated vs untreated comparisonGemma Marinella, Ylenia Vaia, Davide Politano, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 12, 2020
Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patientsGanna Balagura, Antonella Riva, Francesca Marchese, et al.
Annals of Clinical and Translational Neurology|December 2, 2020
Trait impulsivity in Juvenile Myoclonic EpilepsyAmy Shakeshaft, Naim Panjwani, Robert McDowall, et al.
Scientific Reports|February 22, 2022
Sex-specific disease modifiers in juvenile myoclonic epilepsyAmy Shakeshaft, Naim Panjwani, Amber Collingwood, et al.
Pediatrics|November 20, 2025
Evaluation, Diagnosis, and Treatment of Sydenham Chorea: Consensus GuidelinesTerrence Thomas, Michael Eyre, Emanuela Ferrarin, et al.
Orphanet Journal of Rare Diseases|March 8, 2024
Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 childrenAnna Fetta, Francesco Toni, Ilaria Pettenuzzo, et al.
Journal of the Neurological Sciences|March 27, 2021
Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlationsAntonella Riva, Alessandro Orsini, Marcello Scala, et al.
Pageof 11