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Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|January 30, 2007
Prebiotics in human milk: a reviewG V Coppa, L Zampini, T Galeazzi, et al.Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|November 1, 2002
Prebiotics in infant formulas: biochemical characterisation by thin layer chromatography and high performance anion exchange chromatographyG V Coppa, S Bruni, L Zampini, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|November 24, 1999
Oligosaccharides in human milk during different phases of lactationG V Coppa, P Pierani, L Zampini, et al.Advances in Experimental Medicine and Biology|January 15, 2002
Characterization of oligosaccharides in milk and feces of breast-fed infants by high-performance anion-exchange chromatographyG V Coppa, P Pierani, L Zampini, et al.Metabolic Brain Disease|May 29, 2015
Mental retardation in mucopolysaccharidoses correlates with high molecular weight urinary heparan sulphate derived glucosamineG V Coppa, O Gabrielli, L Zampini, et al.Minerva Pediatrica|April 29, 1998
Lactose, oligosaccharide and monosaccharide content of milk from mothers delivering preterm newborns over the first month of lactationG V Coppa, P Pierani, L Zampini, et al.International Journal of Immunopathology and Pharmacology|June 13, 2008
Effects of Holder pasteurization on human milk oligosaccharidesE Bertino, G V Coppa, F Giuliani, et al.European Journal of Pediatrics|January 1, 1989
Oculo-cerebro-cutaneous syndrome: description of a new caseP L Giorgi, O Gabrielli, C Catassi, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1995
Bone marrow transplantation in Hunter syndrome (mucopolysaccharidosis type II): two-year follow-up of the first Italian patient and review of the literatureG V Coppa, O Gabrielli, L Zampini, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 6, 2007
Update on treatment of lysosomal storage diseasesS Bruni, L Loschi, C Incerti, et al.Pageof 10