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EMBO Molecular Medicine|January 6, 2010
Treating lysosomal storage diseases with pharmacological chaperones: from concept to clinicsGiancarlo Parenti
Current Pharmaceutical Biotechnology|January 18, 2011
Pompe disease: from new views on pathophysiology to innovative therapeutic strategiesGiancarlo Parenti, Generoso Andria
Annual Review of Medicine|January 15, 2015
Lysosomal storage diseases: from pathophysiology to therapyGiancarlo Parenti, Generoso Andria, Andrea Ballabio
Italian Journal of Pediatrics|November 17, 2018
New treatments for the mucopolysaccharidoses: from pathophysiology to therapySimona Fecarotta, Serena Gasperini, Giancarlo Parenti
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|October 3, 2012
Universal screening for inherited metabolic diseases in the neonate (and the fetus)Iris Scala, Giancarlo Parenti, Generoso Andria
EMBO Molecular Medicine|January 18, 2021
The rapidly evolving view of lysosomal storage diseasesGiancarlo Parenti, Diego L Medina, Andrea Ballabio
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 17, 2015
Pharmacological Chaperone Therapy: Preclinical Development, Clinical Translation, and Prospects for the Treatment of Lysosomal Storage DisordersGiancarlo Parenti, Generoso Andria, Kenneth J Valenzano
International Journal of Molecular Medicine|November 21, 2012
New strategies for the treatment of lysosomal storage diseases (review)Giancarlo Parenti, Claudio Pignata, Pietro Vajro, et al.
Future Medicinal Chemistry|July 29, 2014
Pharmacological chaperone therapy for lysosomal storage diseasesGiancarlo Parenti, Marco Moracci, Simona Fecarotta, et al.
International Journal of Molecular Sciences|April 9, 2020
Pathogenesis of Mucopolysaccharidoses, an UpdateSimona Fecarotta, Antonietta Tarallo, Carla Damiano, et al.
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