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Vincenzo Leuzzi

Showing results (1-10 of 228) with videos related to

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Journal of Child Neurology|February 25, 2003
Inborn errors of creatine metabolism and epilepsy: clinical features, diagnosis, and treatmentVincenzo Leuzzi
Pediatric Research|January 21, 2022
Looking back at the neonatal period in early-treated phenylketonuric patientsVincenzo Leuzzi, Francesca Nardecchia
Pediatric Neurology|December 27, 2011
Genes of early-onset epileptic encephalopathies: from genotype to phenotypeMario Mastrangelo, Vincenzo Leuzzi
International Review of Neurobiology|July 23, 2023
Experimental pharmacology: Targeting metabolic pathwaysVincenzo Leuzzi, Serena Galosi
Molecular Genetics and Metabolism|February 4, 2010
White matter pathology in phenylketonuriaPeter J Anderson, Vincenzo Leuzzi
Movement Disorders Clinical Practice|February 20, 2020
Treatable Inherited Movement Disorders in Children: Spotlight on Clinical and Biochemical FeaturesSerena Galosi, Francesca Nardecchia, Vincenzo Leuzzi
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 24, 2011
A diagnostic algorithm for the evaluation of early onset genetic-metabolic epileptic encephalopathiesMario Mastrangelo, Andrea Celato, Vincenzo Leuzzi
Neuropediatrics|February 12, 2021
TSC1 as a Novel Gene for Sleep-Related Hypermotor Epilepsy: A Child with a Mild Phenotype of Tuberous SclerosisMario Mastrangelo, Chiara Commone, Carlo Greco, et al.
Parkinsonism & Related Disorders|October 28, 2020
Parkinsonism in children: Clinical classification and etiological spectrumVincenzo Leuzzi, Francesca Nardecchia, Roser Pons, et al.
Epilepsia|November 20, 2012
Inborn errors of creatine metabolism and epilepsyVincenzo Leuzzi, Mario Mastrangelo, Roberta Battini, et al.
Pageof 23

Showing results (1-10 of 228) with videos related to

Sort By:
Pageof 23
Journal of Child Neurology|February 25, 2003
Inborn errors of creatine metabolism and epilepsy: clinical features, diagnosis, and treatmentVincenzo Leuzzi
Pediatric Research|January 21, 2022
Looking back at the neonatal period in early-treated phenylketonuric patientsVincenzo Leuzzi, Francesca Nardecchia
Pediatric Neurology|December 27, 2011
Genes of early-onset epileptic encephalopathies: from genotype to phenotypeMario Mastrangelo, Vincenzo Leuzzi
International Review of Neurobiology|July 23, 2023
Experimental pharmacology: Targeting metabolic pathwaysVincenzo Leuzzi, Serena Galosi
Molecular Genetics and Metabolism|February 4, 2010
White matter pathology in phenylketonuriaPeter J Anderson, Vincenzo Leuzzi
Movement Disorders Clinical Practice|February 20, 2020
Treatable Inherited Movement Disorders in Children: Spotlight on Clinical and Biochemical FeaturesSerena Galosi, Francesca Nardecchia, Vincenzo Leuzzi
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 24, 2011
A diagnostic algorithm for the evaluation of early onset genetic-metabolic epileptic encephalopathiesMario Mastrangelo, Andrea Celato, Vincenzo Leuzzi
Neuropediatrics|February 12, 2021
TSC1 as a Novel Gene for Sleep-Related Hypermotor Epilepsy: A Child with a Mild Phenotype of Tuberous SclerosisMario Mastrangelo, Chiara Commone, Carlo Greco, et al.
Parkinsonism & Related Disorders|October 28, 2020
Parkinsonism in children: Clinical classification and etiological spectrumVincenzo Leuzzi, Francesca Nardecchia, Roser Pons, et al.
Epilepsia|November 20, 2012
Inborn errors of creatine metabolism and epilepsyVincenzo Leuzzi, Mario Mastrangelo, Roberta Battini, et al.
Pageof 23