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Alberto Verrotti

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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|March 30, 2011
Peri-ictal and inter-ictal headache in children and adolescents with idiopathic epilepsy: a multicenter cross-sectional studyAlberto Verrotti, Giangennaro Coppola, Alberto Spalice, et al.
Pediatric Neurology|January 11, 2014
Vaccination and occurrence of seizures in SCN1A mutation-positive patients: a multicenter Italian studyNelia Zamponi, Claudia Passamonti, Cristina Petrelli, et al.
Annals of Human Biology|July 26, 2008
Thirty-year persistence of obesity after presentation to a pediatric obesity clinicLorenzo Iughetti, Michele De Simone, Alberto Verrotti, et al.
Developmental Medicine and Child Neurology|September 24, 2008
Levetiracetam in absence epilepsyAlberto Verrotti, Caterina Cerminara, Sergio Domizio, et al.
Italian Journal of Pediatrics|June 5, 2017
Current role of perampanel in pediatric epilepsyPaola De Liso, Romina Moavero, Giangennaro Coppola, et al.
BMC Medical Genomics|August 17, 2022
Expanding the genetic and clinical characteristics of Protocadherin 19 gene mutationsGiovanni Battista Dell'Isola, Elisabetta Mencaroni, Antonella Fattorusso, et al.
Journal of Perinatal Medicine|December 4, 2004
Prolonged fetal bradycardia as the presenting clinical sign in Streptococcus agalactiae chorioamnionitisGiuseppe Presta, Enrico Rosati, Raffaella Giannuzzi, et al.
Journal of Clinical Medicine|August 10, 2024
Isolated Intracranial Hypertensions as Onset of Myelin Oligodendrocyte Glycoprotein Antibody DiseaseLaura Papetti, Giulia Moltoni, Daniela Longo, et al.
World Journal of Pediatrics : WJP|January 17, 2023
Clinical spectrum and currently available treatment of type I interferonopathy Aicardi-Goutières syndromeGiovanni Battista Dell'Isola, Gianluca Dini, Kaleb Logan Culpepper, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 24, 2018
A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotypeGiulia Iapadre, Giovanni Morana, Maria Stella Vari, et al.
Pageof 45

Showing results (311-320 of 447) with videos related to

Sort By:
Pageof 45
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|March 30, 2011
Peri-ictal and inter-ictal headache in children and adolescents with idiopathic epilepsy: a multicenter cross-sectional studyAlberto Verrotti, Giangennaro Coppola, Alberto Spalice, et al.
Pediatric Neurology|January 11, 2014
Vaccination and occurrence of seizures in SCN1A mutation-positive patients: a multicenter Italian studyNelia Zamponi, Claudia Passamonti, Cristina Petrelli, et al.
Annals of Human Biology|July 26, 2008
Thirty-year persistence of obesity after presentation to a pediatric obesity clinicLorenzo Iughetti, Michele De Simone, Alberto Verrotti, et al.
Developmental Medicine and Child Neurology|September 24, 2008
Levetiracetam in absence epilepsyAlberto Verrotti, Caterina Cerminara, Sergio Domizio, et al.
Italian Journal of Pediatrics|June 5, 2017
Current role of perampanel in pediatric epilepsyPaola De Liso, Romina Moavero, Giangennaro Coppola, et al.
BMC Medical Genomics|August 17, 2022
Expanding the genetic and clinical characteristics of Protocadherin 19 gene mutationsGiovanni Battista Dell'Isola, Elisabetta Mencaroni, Antonella Fattorusso, et al.
Journal of Perinatal Medicine|December 4, 2004
Prolonged fetal bradycardia as the presenting clinical sign in Streptococcus agalactiae chorioamnionitisGiuseppe Presta, Enrico Rosati, Raffaella Giannuzzi, et al.
Journal of Clinical Medicine|August 10, 2024
Isolated Intracranial Hypertensions as Onset of Myelin Oligodendrocyte Glycoprotein Antibody DiseaseLaura Papetti, Giulia Moltoni, Daniela Longo, et al.
World Journal of Pediatrics : WJP|January 17, 2023
Clinical spectrum and currently available treatment of type I interferonopathy Aicardi-Goutières syndromeGiovanni Battista Dell'Isola, Gianluca Dini, Kaleb Logan Culpepper, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 24, 2018
A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotypeGiulia Iapadre, Giovanni Morana, Maria Stella Vari, et al.
Pageof 45