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Federica Deodato

Showing results (1-10 of 58) with videos related to

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International Journal of Molecular Sciences|April 29, 2020
Intravenous Enzyme Replacement Therapy in Mucopolysaccharidoses: Clinical Effectiveness and LimitationsRossella Parini, Federica Deodato
Italian Journal of Pediatrics|November 17, 2018
Enzyme replacement therapy: efficacy and limitationsDaniela Concolino, Federica Deodato, Rossella Parini
Journal of Inherited Metabolic Disease|July 16, 2010
Cobalamin C defect: natural history, pathophysiology, and treatmentDiego Martinelli, Federica Deodato, Carlo Dionisi-Vici
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 8, 2006
Methylmalonic and propionic aciduriaFederica Deodato, Sara Boenzi, Filippo M Santorelli, et al.
Journal of Inherited Metabolic Disease|June 10, 2006
'Classical' organic acidurias, propionic aciduria, methylmalonic aciduria and isovaleric aciduria: long-term outcome and effects of expanded newborn screening using tandem mass spectrometryCarlo Dionisi-Vici, Federica Deodato, Wulf Röschinger, et al.
Frontiers in Pediatrics|January 21, 2025
Case Report: Two years of compassionate use with Olipudase-alfa in a child with neurovisceral acid sphingomyelinase deficiencyFederica Deodato, Sara Boenzi, Benedetta Greco, et al.
Molecular Genetics and Metabolism|November 23, 2021
Comprehensive-targeted lipidomic analysis in Niemann-Pick C diseaseSara Boenzi, Giulio Catesini, Elisa Sacchetti, et al.
Pediatric Blood & Cancer|August 19, 2014
Early diagnosis of Gaucher disease in pediatric patients: proposal for a diagnostic algorithmMaja Di Rocco, Generoso Andria, Federica Deodato, et al.
Journal of Lipid Research|January 7, 2016
Evaluation of plasma cholestane-3β,5α,6β-triol and 7-ketocholesterol in inherited disorders related to cholesterol metabolismSara Boenzi, Federica Deodato, Roberta Taurisano, et al.
Journal of Child Neurology|April 27, 2013
Immune tolerance induced using plasma exchange and rituximab in an infantile Pompe disease patientFederica Deodato, Virginia Maria Ginocchio, Alfredo Onofri, et al.
Pageof 6

Showing results (1-10 of 58) with videos related to

Sort By:
Pageof 6
International Journal of Molecular Sciences|April 29, 2020
Intravenous Enzyme Replacement Therapy in Mucopolysaccharidoses: Clinical Effectiveness and LimitationsRossella Parini, Federica Deodato
Italian Journal of Pediatrics|November 17, 2018
Enzyme replacement therapy: efficacy and limitationsDaniela Concolino, Federica Deodato, Rossella Parini
Journal of Inherited Metabolic Disease|July 16, 2010
Cobalamin C defect: natural history, pathophysiology, and treatmentDiego Martinelli, Federica Deodato, Carlo Dionisi-Vici
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 8, 2006
Methylmalonic and propionic aciduriaFederica Deodato, Sara Boenzi, Filippo M Santorelli, et al.
Journal of Inherited Metabolic Disease|June 10, 2006
'Classical' organic acidurias, propionic aciduria, methylmalonic aciduria and isovaleric aciduria: long-term outcome and effects of expanded newborn screening using tandem mass spectrometryCarlo Dionisi-Vici, Federica Deodato, Wulf Röschinger, et al.
Frontiers in Pediatrics|January 21, 2025
Case Report: Two years of compassionate use with Olipudase-alfa in a child with neurovisceral acid sphingomyelinase deficiencyFederica Deodato, Sara Boenzi, Benedetta Greco, et al.
Molecular Genetics and Metabolism|November 23, 2021
Comprehensive-targeted lipidomic analysis in Niemann-Pick C diseaseSara Boenzi, Giulio Catesini, Elisa Sacchetti, et al.
Pediatric Blood & Cancer|August 19, 2014
Early diagnosis of Gaucher disease in pediatric patients: proposal for a diagnostic algorithmMaja Di Rocco, Generoso Andria, Federica Deodato, et al.
Journal of Lipid Research|January 7, 2016
Evaluation of plasma cholestane-3β,5α,6β-triol and 7-ketocholesterol in inherited disorders related to cholesterol metabolismSara Boenzi, Federica Deodato, Roberta Taurisano, et al.
Journal of Child Neurology|April 27, 2013
Immune tolerance induced using plasma exchange and rituximab in an infantile Pompe disease patientFederica Deodato, Virginia Maria Ginocchio, Alfredo Onofri, et al.
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