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Francesca Ragona

Showing results (51-60 of 87) with videos related to

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Acta Neurologica Scandinavica|August 16, 2018
Electroclinical features of epilepsy monosomy 1p36 syndrome and their implicationsAlberto Verrotti, Marco Greco, Gaia Varriale, et al.
Epilepsia Open|July 2, 2024
Unraveling unmet needs in ketogenic dietary services: An ERN EpiCARE surveyValentina De Giorgis, Ludovica Pasca, Gemma Aznar-Lain, et al.
Epilepsia|December 31, 2024
Fenfluramine treatment for Dravet syndrome: Long term real-world analysis demonstrates safety and reduced health care burdenAlessandra Boncristiano, Simona Balestrini, Viola Doccini, et al.
Neurobiology of Disease|June 25, 2018
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitabilityMattia Bonzanni, Jacopo C DiFrancesco, Raffaella Milanesi, 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.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 5, 2019
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center studyRoberto Di Marco, Ann Hallemans, Giulia Bellon, 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.
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.
Frontiers in Molecular Neuroscience|August 22, 2018
A Loss-of-Function <i>HCN4</i> Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal ExcitabilityGiulia Campostrini, Jacopo C DiFrancesco, Barbara Castellotti, et al.
Human Mutation|May 16, 2014
VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathiesDaria Diodato, Laura Melchionda, Tobias B Haack, et al.
Pageof 9

Showing results (51-60 of 87) with videos related to

Sort By:
Pageof 9
Acta Neurologica Scandinavica|August 16, 2018
Electroclinical features of epilepsy monosomy 1p36 syndrome and their implicationsAlberto Verrotti, Marco Greco, Gaia Varriale, et al.
Epilepsia Open|July 2, 2024
Unraveling unmet needs in ketogenic dietary services: An ERN EpiCARE surveyValentina De Giorgis, Ludovica Pasca, Gemma Aznar-Lain, et al.
Epilepsia|December 31, 2024
Fenfluramine treatment for Dravet syndrome: Long term real-world analysis demonstrates safety and reduced health care burdenAlessandra Boncristiano, Simona Balestrini, Viola Doccini, et al.
Neurobiology of Disease|June 25, 2018
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitabilityMattia Bonzanni, Jacopo C DiFrancesco, Raffaella Milanesi, 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.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 5, 2019
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center studyRoberto Di Marco, Ann Hallemans, Giulia Bellon, 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.
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.
Frontiers in Molecular Neuroscience|August 22, 2018
A Loss-of-Function <i>HCN4</i> Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal ExcitabilityGiulia Campostrini, Jacopo C DiFrancesco, Barbara Castellotti, et al.
Human Mutation|May 16, 2014
VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathiesDaria Diodato, Laura Melchionda, Tobias B Haack, et al.
Pageof 9