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Journal of Inherited Metabolic Disease|April 30, 2010
Pathophysiology of neuropathic lysosomal storage disordersCinzia Maria Bellettato, Maurizio ScarpaItalian Journal of Pediatrics|November 17, 2018
Possible strategies to cross the blood-brain barrierCinzia M Bellettato, Maurizio ScarpaJournal of Pediatric Rehabilitation Medicine|July 28, 2011
Evaluation of disease severity in mucopolysaccharidosesMichael Beck, Joseph Muenzer, Maurizio ScarpaMolecular Genetics and Metabolism|November 25, 2017
Epilepsy in mucopolysaccharidosis disordersMaurizio Scarpa, Charles Marques Lourenço, Hernán AmartinoMolecular Genetics and Metabolism Reports|December 6, 2023
Relief of nocturnal neuropathic pain with the use of cannabis in a patient with Fabry diseaseMartina Bon, Andrea Dardis, Maurizio Scarpa, et al.Current Pharmaceutical Design|August 5, 2008
Lysosomal storage diseases and the blood-brain barrierDavid J Begley, Charles C Pontikis, Maurizio ScarpaRheumatic Diseases Clinics of North America|April 20, 2013
Mucopolysaccharidoses and other lysosomal storage diseasesChristina Lampe, Cinzia Maria Bellettato, Nesrin Karabul, et al.Orphanet Journal of Rare Diseases|April 21, 2020
Assessing the impact of the five senses on quality of life in mucopolysaccharidosesRoberto Giugliani, Paul Harmatz, Shuan-Pei Lin, et al.Pediatric Clinics of North America|March 6, 2018
Inborn Errors of Metabolism Involving Complex Molecules: Lysosomal and Peroxisomal Storage DiseasesCinzia Maria Bellettato, Leroy Hubert, Maurizio Scarpa, et al.JIMD Reports|January 14, 2015
The biological clock and the molecular basis of lysosomal storage diseasesGianluigi Mazzoccoli, Tommaso Mazza, Manlio Vinciguerra, et al.Pageof 15