GASPARRI, MANUELA
GASPARRI, MANUELA
Universita' degli Studi di MILANO
Use of fibroscan in monitoring liver impairment in glycogen storage disease type I and III
2013 S. Paci, M. Gasparri, S. Pieretti, V. Rovelli, E. Riva, E. Salvatici
Efficacy of enzyme replacement therapy over six-months in a non-classic infantile Pompe disease form: our experience in a 2-year-old affected child
2013 S. Paci, V. Scelsa, M. Gasparri, E. Salvatici
A case of glycogenosis type IB associated with MGUS
2011 E. Riva, M. Gasparri, I. Giulini Neri, S. Paci
Bone mineralization in type 1 glycogen storage disease: a two years follow up study
2010 E. Riva, I. Giulini Neri, M. Gasparri, J. Scotti Gerber, E. Salvatici, D. Minghetti, G. Cagnoli, S. Paci
Case report: GSD type 1. and pregnancy
2008 S. Paci, M. Gasparri, I. Giulini Neri, M. Bonza, E. Salvatici, M. Giovannini
Mineralizzazione ossea in pazienti con GSD 1. e 3.
2008 S. Paci, M. Bonza, M. Gasparri, I. Giulini Neri, E. Salvatici, E. Riva
Absence of severe recurrent infections in GSD IB
2008 S. Paci, M. Gasparri, I. Giulini Neri, G. Cagnoli, E. Salvatici, M. Giovannini
Bone mineralization in GSD I and III
2008 E. Riva, S. Paci, I. Giulini Neri, M. Gasparri, G. Cagnoli, M. Bonza, C. Agostoni
Amino acid status 6 hours after the assumption of two amino acid preparations in PKU patients on diet-therapy
2007 M. Giovannini, D. Casero, S. Paci, M. Gasparri, S. El Oksha, M. Bonza, A.M. Lammardo, E. Salvatici, C. Agostoni
Assetto lipidico nei pazienti con glicogenosi: l'esperienza della Clinica Pediatrica dell'Ospedale San Paolo
2006 S. Paci, I. Giulini Neri, M. Gasparri, M. Torcoletti, M. Giovannini