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Vincenzo Leuzzi

Showing results (11-20 of 228) with videos related to

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Movement Disorders Clinical Practice|April 15, 2024
Reply to: Partially Levodopa-Responsive Parkinsonism in a Carrier of a Novel Pathogenic CLTC VariantFrancesca Nardecchia, Simone Martinelli, Luca Pollini, et al.
Movement Disorders Clinical Practice|January 10, 2022
Neurodevelopmental Disorder and Late-Onset Degenerative Parkinsonism in a Patient with a <i>WDR45</i> DefectFilippo Manti, Celeste Panteghini, Barbara Garavaglia, et al.
Parkinsonism & Related Disorders|October 1, 2024
Pediatric parkinsonism: In-depth clinical definition and semeiologyVincenzo Leuzzi, Maria Novelli, Ivana Paparella, 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.
International Journal of Molecular Sciences|April 30, 2021
Genetic Neonatal-Onset Epilepsies and Developmental/Epileptic Encephalopathies with Movement Disorders: A Systematic ReviewCarlotta Spagnoli, Carlo Fusco, Antonio Percesepe, et al.
Journal of Inherited Metabolic Disease|March 31, 2016
Erythrocyte-mediated delivery of recombinant enzymesVincenzo Leuzzi, Luigia Rossi, Claudia Gabucci, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 24, 2013
Running apraxia as a presenting symptom of neuronal ceroid lipofuscinosis 6Vincenzo Leuzzi, Barbara Garavaglia, Filippo Manti, et al.
Molecular Genetics and Metabolism|June 19, 2019
Clinical characterization of tremor in patients with phenylketonuriaFrancesca Nardecchia, Filippo Manti, Sabrina De Leo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 8, 2013
Transdermal rotigotine in the treatment of aromatic L-amino acid decarboxylase deficiencyMario Mastrangelo, Caterina Caputi, Serena Galosi, et al.
Analytical Biochemistry|February 9, 2008
Arginine and glycine stimulate creatine synthesis in creatine transporter 1-deficient lymphoblastsVincenzo Leuzzi, Maria G Alessandrì, Manuela Casarano, et al.
Pageof 23

Showing results (11-20 of 228) with videos related to

Sort By:
Pageof 23
Movement Disorders Clinical Practice|April 15, 2024
Reply to: Partially Levodopa-Responsive Parkinsonism in a Carrier of a Novel Pathogenic CLTC VariantFrancesca Nardecchia, Simone Martinelli, Luca Pollini, et al.
Movement Disorders Clinical Practice|January 10, 2022
Neurodevelopmental Disorder and Late-Onset Degenerative Parkinsonism in a Patient with a <i>WDR45</i> DefectFilippo Manti, Celeste Panteghini, Barbara Garavaglia, et al.
Parkinsonism & Related Disorders|October 1, 2024
Pediatric parkinsonism: In-depth clinical definition and semeiologyVincenzo Leuzzi, Maria Novelli, Ivana Paparella, 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.
International Journal of Molecular Sciences|April 30, 2021
Genetic Neonatal-Onset Epilepsies and Developmental/Epileptic Encephalopathies with Movement Disorders: A Systematic ReviewCarlotta Spagnoli, Carlo Fusco, Antonio Percesepe, et al.
Journal of Inherited Metabolic Disease|March 31, 2016
Erythrocyte-mediated delivery of recombinant enzymesVincenzo Leuzzi, Luigia Rossi, Claudia Gabucci, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 24, 2013
Running apraxia as a presenting symptom of neuronal ceroid lipofuscinosis 6Vincenzo Leuzzi, Barbara Garavaglia, Filippo Manti, et al.
Molecular Genetics and Metabolism|June 19, 2019
Clinical characterization of tremor in patients with phenylketonuriaFrancesca Nardecchia, Filippo Manti, Sabrina De Leo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 8, 2013
Transdermal rotigotine in the treatment of aromatic L-amino acid decarboxylase deficiencyMario Mastrangelo, Caterina Caputi, Serena Galosi, et al.
Analytical Biochemistry|February 9, 2008
Arginine and glycine stimulate creatine synthesis in creatine transporter 1-deficient lymphoblastsVincenzo Leuzzi, Maria G Alessandrì, Manuela Casarano, et al.
Pageof 23