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Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseases.
Belfiore MP, Iacobellis F, Acampora E, Caiazza M, Rubino M, Monda E, Magaldi MR, Tarallo A, Sasso M, De Pasquale V, Grassi R, Cappabianca S, Calabrò P, Fecarotta S, Esposito S, Esposito G, Pisani A, Pavone LM, Parenti G, Limongelli G. Belfiore MP, et al. Among authors: parenti g. PLoS One. 2020 May 19;15(5):e0233050. doi: 10.1371/journal.pone.0233050. eCollection 2020. PLoS One. 2020. PMID: 32428018 Free PMC article.
Chronic diarrhea in mucopolysaccharidosis IIIB.
Sibilio M, Miele E, Ungaro C, Astarita L, Turco R, Di Natale P, Pontarelli G, Vecchione R, Andria G, Staiano A, Parenti G. Sibilio M, et al. Among authors: parenti g. J Pediatr Gastroenterol Nutr. 2009 Oct;49(4):477-80. doi: 10.1097/MPG.0b013e31818a082a. J Pediatr Gastroenterol Nutr. 2009. PMID: 19516195 No abstract available.
Synergy between the pharmacological chaperone 1-deoxygalactonojirimycin and the human recombinant alpha-galactosidase A in cultured fibroblasts from patients with Fabry disease.
Porto C, Pisani A, Rosa M, Acampora E, Avolio V, Tuzzi MR, Visciano B, Gagliardo C, Materazzi S, la Marca G, Andria G, Parenti G. Porto C, et al. Among authors: parenti g. J Inherit Metab Dis. 2012 May;35(3):513-20. doi: 10.1007/s10545-011-9424-3. Epub 2011 Dec 21. J Inherit Metab Dis. 2012. PMID: 22187137
414 results