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Molecular Genetics and Metabolism|February 4, 2010
White matter pathology in phenylketonuriaPeter J Anderson, Vincenzo LeuzziJournal of Child Neurology|February 25, 2003
Inborn errors of creatine metabolism and epilepsy: clinical features, diagnosis, and treatmentVincenzo LeuzziPediatric Neurology|December 27, 2011
Genes of early-onset epileptic encephalopathies: from genotype to phenotypeMario Mastrangelo, Vincenzo LeuzziInternational Review of Neurobiology|July 23, 2023
Experimental pharmacology: Targeting metabolic pathwaysVincenzo Leuzzi, Serena GalosiMovement Disorders Clinical Practice|February 20, 2020
Treatable Inherited Movement Disorders in Children: Spotlight on Clinical and Biochemical FeaturesSerena Galosi, Francesca Nardecchia, Vincenzo LeuzziEuropean 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 LeuzziNeuropediatrics|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.Molecular Genetics and Metabolism|September 6, 2023
Metabolic control and clinical outcome in adolescents with phenylketonuriaAgnese De Giorgi, Francesca Nardecchia, Cristina Romani, et al.Pageof 64