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Journal of Child Neurology
|
February 25, 2003
Inborn errors of creatine metabolism and epilepsy: clinical features, diagnosis, and treatment
Vincenzo Leuzzi
Pediatric Research
|
January 21, 2022
Looking back at the neonatal period in early-treated phenylketonuric patients
Vincenzo Leuzzi, Francesca Nardecchia
Pediatric Neurology
|
December 27, 2011
Genes of early-onset epileptic encephalopathies: from genotype to phenotype
Mario Mastrangelo, Vincenzo Leuzzi
International Review of Neurobiology
|
July 23, 2023
Experimental pharmacology: Targeting metabolic pathways
Vincenzo Leuzzi, Serena Galosi
Molecular Genetics and Metabolism
|
February 4, 2010
White matter pathology in phenylketonuria
Peter J Anderson, Vincenzo Leuzzi
Movement Disorders Clinical Practice
|
February 20, 2020
Treatable Inherited Movement Disorders in Children: Spotlight on Clinical and Biochemical Features
Serena 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 encephalopathies
Mario 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 Sclerosis
Mario Mastrangelo, Chiara Commone, Carlo Greco, et al.
Parkinsonism & Related Disorders
|
October 28, 2020
Parkinsonism in children: Clinical classification and etiological spectrum
Vincenzo Leuzzi, Francesca Nardecchia, Roser Pons, et al.
Epilepsia
|
November 20, 2012
Inborn errors of creatine metabolism and epilepsy
Vincenzo Leuzzi, Mario Mastrangelo, Roberta Battini, et al.
Page
of 23
Search research articles
Search
Showing results (1-10 of 228) with videos related to
Sort By:
Page
of 23
Journal of Child Neurology
|
February 25, 2003
Inborn errors of creatine metabolism and epilepsy: clinical features, diagnosis, and treatment
Vincenzo Leuzzi
Pediatric Research
|
January 21, 2022
Looking back at the neonatal period in early-treated phenylketonuric patients
Vincenzo Leuzzi, Francesca Nardecchia
Pediatric Neurology
|
December 27, 2011
Genes of early-onset epileptic encephalopathies: from genotype to phenotype
Mario Mastrangelo, Vincenzo Leuzzi
International Review of Neurobiology
|
July 23, 2023
Experimental pharmacology: Targeting metabolic pathways
Vincenzo Leuzzi, Serena Galosi
Molecular Genetics and Metabolism
|
February 4, 2010
White matter pathology in phenylketonuria
Peter J Anderson, Vincenzo Leuzzi
Movement Disorders Clinical Practice
|
February 20, 2020
Treatable Inherited Movement Disorders in Children: Spotlight on Clinical and Biochemical Features
Serena 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 encephalopathies
Mario 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 Sclerosis
Mario Mastrangelo, Chiara Commone, Carlo Greco, et al.
Parkinsonism & Related Disorders
|
October 28, 2020
Parkinsonism in children: Clinical classification and etiological spectrum
Vincenzo Leuzzi, Francesca Nardecchia, Roser Pons, et al.
Epilepsia
|
November 20, 2012
Inborn errors of creatine metabolism and epilepsy
Vincenzo Leuzzi, Mario Mastrangelo, Roberta Battini, et al.
Page
of 23