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Francesca Ragona

Showing results (71-80 of 87) with videos related to

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Epilepsia|March 27, 2007
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlationsPasquale Striano, Maria Margherita Mancardi, Roberta Biancheri, et al.
Epilepsy Research|August 26, 2019
An Italian multicentre study of perampanel in progressive myoclonus epilepsiesLaura Canafoglia, Giuseppina Barbella, Edoardo Ferlazzo, et al.
Epilepsia Open|March 20, 2023
A registry for Dravet syndrome: The Italian experienceSimona Balestrini, Viola Doccini, Sabrina Giometto, et al.
Journal of Medical Genetics|November 29, 2024
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in ItalyDavide Mei, Simona Balestrini, Elena Parrini, et al.
Pediatric Neurology|February 11, 2023
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional StudyIrene Toldo, Francesco Brunello, Paola Cavasin, et al.
Epilepsia|November 20, 2018
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter studyMarina Trivisano, Nicola Pietrafusa, Alessandra Terracciano, et al.
Brain : a Journal of Neurology|August 23, 2015
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotypeFatima Jaffer, Andreja Avbersek, Rosaria Vavassori, et al.
Epilepsia|October 21, 2016
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre studyMarilena Vecchi, Carmen Barba, Debora De Carlo, et al.
Annals of Neurology|April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel propertiesKaren L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Medrxiv : the Preprint Server for Health Sciences|September 10, 2024
Children and Adolescent Patients with Variants in the <i>ATP1A3</i> -encoded Sodium-Potassium ATPase Alpha-3 Subunit Demonstrate an Impaired QT Response to Bradycardia and Predisposition to Sinus Node DysfunctionMeredith K Srour, Minu-Tshyeto K Bidzimou, Padmapriya Muralidharan, et al.
Pageof 9

Showing results (71-80 of 87) with videos related to

Sort By:
Pageof 9
Epilepsia|March 27, 2007
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlationsPasquale Striano, Maria Margherita Mancardi, Roberta Biancheri, et al.
Epilepsy Research|August 26, 2019
An Italian multicentre study of perampanel in progressive myoclonus epilepsiesLaura Canafoglia, Giuseppina Barbella, Edoardo Ferlazzo, et al.
Epilepsia Open|March 20, 2023
A registry for Dravet syndrome: The Italian experienceSimona Balestrini, Viola Doccini, Sabrina Giometto, et al.
Journal of Medical Genetics|November 29, 2024
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in ItalyDavide Mei, Simona Balestrini, Elena Parrini, et al.
Pediatric Neurology|February 11, 2023
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional StudyIrene Toldo, Francesco Brunello, Paola Cavasin, et al.
Epilepsia|November 20, 2018
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter studyMarina Trivisano, Nicola Pietrafusa, Alessandra Terracciano, et al.
Brain : a Journal of Neurology|August 23, 2015
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotypeFatima Jaffer, Andreja Avbersek, Rosaria Vavassori, et al.
Epilepsia|October 21, 2016
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre studyMarilena Vecchi, Carmen Barba, Debora De Carlo, et al.
Annals of Neurology|April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel propertiesKaren L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Medrxiv : the Preprint Server for Health Sciences|September 10, 2024
Children and Adolescent Patients with Variants in the <i>ATP1A3</i> -encoded Sodium-Potassium ATPase Alpha-3 Subunit Demonstrate an Impaired QT Response to Bradycardia and Predisposition to Sinus Node DysfunctionMeredith K Srour, Minu-Tshyeto K Bidzimou, Padmapriya Muralidharan, et al.
Pageof 9