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Francesca Ragona

Showing results (81-90 of 87) with videos related to

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Frontiers in Neurology|June 7, 2021
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox-Gastaut SyndromeLuigi Francesco Iannone, Gabriele Arena, Domenica Battaglia, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|November 29, 2022
Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGADMargherita Nosadini, Michael Eyre, Thea Giacomini, et al.
Neurology|March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic VariantsNiklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
JAMA Pediatrics|March 3, 2025
ATP1A3 Variants, Variably Penetrant Short QT Intervals, and Lethal Ventricular ArrhythmiasMary E Moya-Mendez, Minu-Tshyeto Bidzimou, Padmapriya Muralidharan, et al.
Neurology|September 11, 2020
Cardiac phenotype in <i>ATP1A3</i>-related syndromes: A multicenter cohort studySimona Balestrini, Mohamad A Mikati, Reyes Álvarez-García-Rovés, et al.
Brain : a Journal of Neurology|October 24, 2018
HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyondCarla Marini, Alessandro Porro, Agnès Rastetter, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
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Showing results (81-90 of 87) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 87 results.
Frontiers in Neurology|June 7, 2021
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox-Gastaut SyndromeLuigi Francesco Iannone, Gabriele Arena, Domenica Battaglia, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|November 29, 2022
Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGADMargherita Nosadini, Michael Eyre, Thea Giacomini, et al.
Neurology|March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic VariantsNiklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
JAMA Pediatrics|March 3, 2025
ATP1A3 Variants, Variably Penetrant Short QT Intervals, and Lethal Ventricular ArrhythmiasMary E Moya-Mendez, Minu-Tshyeto Bidzimou, Padmapriya Muralidharan, et al.
Neurology|September 11, 2020
Cardiac phenotype in <i>ATP1A3</i>-related syndromes: A multicenter cohort studySimona Balestrini, Mohamad A Mikati, Reyes Álvarez-García-Rovés, et al.
Brain : a Journal of Neurology|October 24, 2018
HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyondCarla Marini, Alessandro Porro, Agnès Rastetter, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
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