O Gabrielli|I Carloni|G V Coppa - JoVE Visualize

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Neuroradiology|January 1, 1993

Morphological studies of the corpus callosum by MRI in children with malformative syndromesO Gabrielli, U Salvolini, V Bonifazi, et al.

Helvetica Paediatrica Acta|June 1, 1987

Clinical application of a new simple method for the identification of mucopolysaccharidosesG V Coppa, C Catassi, O Gabrielli, et al.

Pediatric Radiology|January 1, 1990

Magnetic resonance imaging in the malformative syndromes with mental retardationO Gabrielli, U Salvolini, G V Coppa, et al.

Pathologica|July 1, 1992

[A case of focal necrotizing granulomatous hepatitis in childhood]O Gabrielli, I Carloni, P F Gentilucci, et al.

Lancet (London, England)|March 10, 1990

Preliminary study of breastfeeding and bacterial adhesion to uroepithelial cellsG V Coppa, O Gabrielli, P Giorgi, et al.

European Journal of Pediatrics|April 1, 1983

Clinical heterogeneity in Sanfilippo disease (mucopolysaccharidosis III) type D: presentation of two new casesG V Coppa, P L Giorgi, L Felici, 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.

Minerva Pediatrica|April 1, 1995

[Echographic and sonographic study of ovaries in girls with precocious puberty]G Ciotti, O Gabrielli, I Carloni, 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.

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.

Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:

Pageof 9

Neuroradiology|January 1, 1993

Morphological studies of the corpus callosum by MRI in children with malformative syndromesO Gabrielli, U Salvolini, V Bonifazi, et al.

Helvetica Paediatrica Acta|June 1, 1987

Clinical application of a new simple method for the identification of mucopolysaccharidosesG V Coppa, C Catassi, O Gabrielli, et al.

Pediatric Radiology|January 1, 1990

Magnetic resonance imaging in the malformative syndromes with mental retardationO Gabrielli, U Salvolini, G V Coppa, et al.

Pathologica|July 1, 1992

[A case of focal necrotizing granulomatous hepatitis in childhood]O Gabrielli, I Carloni, P F Gentilucci, et al.

Lancet (London, England)|March 10, 1990

Preliminary study of breastfeeding and bacterial adhesion to uroepithelial cellsG V Coppa, O Gabrielli, P Giorgi, et al.

European Journal of Pediatrics|April 1, 1983

Clinical heterogeneity in Sanfilippo disease (mucopolysaccharidosis III) type D: presentation of two new casesG V Coppa, P L Giorgi, L Felici, 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.

Minerva Pediatrica|April 1, 1995

[Echographic and sonographic study of ovaries in girls with precocious puberty]G Ciotti, O Gabrielli, I Carloni, 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.

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.

Pageof 9