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O Gabrielli

Showing results (11-20 of 70) with videos related to

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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.
European Journal of Pediatrics|January 1, 1989
Oculo-cerebro-cutaneous syndrome: description of a new caseP L Giorgi, O Gabrielli, C Catassi, et al.
Pathologica|May 1, 1989
[Type-III acrocephalosyndactylia (Saethre-Chotzen syndrome). Description of 2 cases]O Gabrielli, E Moroni, M Barbato, 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 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.
American Journal of Medical Genetics|August 1, 1991
Intestinal lymphangiectasia, lymphedema, mental retardation, and typical face: confirmation of the Hennekam syndromeO Gabrielli, C Catassi, A Carlucci, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1981
[Enzymatic diagnosis of classical Morquio syndrome (mucopolysaccharidosis IV A) (author's transl)]G V Coppa, L Felici, M Emanuelli, et al.
American Journal of Medical Genetics|February 1, 1990
Mild form of Jeune syndrome in two sistersP L Giorgi, O Gabrielli, V Bonifazi, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|September 1, 1994
Characterization of carbohydrates in commercial infant formulaeG V Coppa, O Gabrielli, P Pierani, et al.
Minerva Pediatrica|September 24, 2013
Hunter syndrome (Mucopolysaccharidosis type II), severe phenotype: long term follow-up on patients undergone to hematopoietic stem cell transplantationR Annibali, L Caponi, A Morganti, et al.
Pageof 7

Showing results (11-20 of 70) with videos related to

Sort By:
Pageof 7
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.
European Journal of Pediatrics|January 1, 1989
Oculo-cerebro-cutaneous syndrome: description of a new caseP L Giorgi, O Gabrielli, C Catassi, et al.
Pathologica|May 1, 1989
[Type-III acrocephalosyndactylia (Saethre-Chotzen syndrome). Description of 2 cases]O Gabrielli, E Moroni, M Barbato, 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 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.
American Journal of Medical Genetics|August 1, 1991
Intestinal lymphangiectasia, lymphedema, mental retardation, and typical face: confirmation of the Hennekam syndromeO Gabrielli, C Catassi, A Carlucci, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1981
[Enzymatic diagnosis of classical Morquio syndrome (mucopolysaccharidosis IV A) (author's transl)]G V Coppa, L Felici, M Emanuelli, et al.
American Journal of Medical Genetics|February 1, 1990
Mild form of Jeune syndrome in two sistersP L Giorgi, O Gabrielli, V Bonifazi, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|September 1, 1994
Characterization of carbohydrates in commercial infant formulaeG V Coppa, O Gabrielli, P Pierani, et al.
Minerva Pediatrica|September 24, 2013
Hunter syndrome (Mucopolysaccharidosis type II), severe phenotype: long term follow-up on patients undergone to hematopoietic stem cell transplantationR Annibali, L Caponi, A Morganti, et al.
Pageof 7