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Renzo Galanello

Showing results (41-50 of 113) with videos related to

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Haematologica|October 14, 2003
Thalassemia minor, the Gilbert mutation, and the risk of gallstonesCaterina Borgna-Pignatti, Francesca Rigon, Luciano Merlo, et al.
Haematologica|November 12, 2009
Pregnancy and beta-thalassemia: an Italian multicenter experienceRaffaella Origa, Antonio Piga, Giovanni Quarta, et al.
British Journal of Haematology|November 30, 2004
Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patientsRenzo Galanello, Lucia Perseu, Chiara Perra, et al.
Haematologica|August 10, 2012
Toward optimizing the use of deferasirox: potential benefits of combined use with deferoxamineRobert W Grady, Renzo Galanello, Rachel E Randolph, et al.
Acta Haematologica|November 13, 2013
α-globin gene quadruplication and heterozygous β-thalassemia: a not so rare cause of thalassemia intermediaRaffaella Origa, Maria Carla Sollaino, Caterina Borgna-Pignatti, et al.
Haematologica|January 18, 2015
Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermediaRaffaella Origa, Mario Cazzola, Elisabetta Mereu, et al.
Blood Cells, Molecules & Diseases|July 31, 2013
Complexity of the alpha-globin genotypes identified with thalassemia screening in SardiniaRaffaella Origa, Maria E Paglietti, Maria C Sollaino, et al.
European Journal of Internal Medicine|November 8, 2015
Development of a new disease severity scoring system for patients with non-transfusion-dependent thalassemiaM Domenica Cappellini, John B Porter, Khaled M Musallam, et al.
Haematologica|September 8, 2006
A prospective randomized controlled trial on the safety and efficacy of alternating deferoxamine and deferiprone in the treatment of iron overload in patients with thalassemiaRenzo Galanello, Antonis Kattamis, Antonio Piga, et al.
Human Gene Therapy|December 19, 2006
Therapeutic options for patients with severe beta-thalassemia: the need for globin gene therapyMichel Sadelain, Farid Boulad, Renzo Galanello, et al.
Pageof 12

Showing results (41-50 of 113) with videos related to

Sort By:
Pageof 12
Haematologica|October 14, 2003
Thalassemia minor, the Gilbert mutation, and the risk of gallstonesCaterina Borgna-Pignatti, Francesca Rigon, Luciano Merlo, et al.
Haematologica|November 12, 2009
Pregnancy and beta-thalassemia: an Italian multicenter experienceRaffaella Origa, Antonio Piga, Giovanni Quarta, et al.
British Journal of Haematology|November 30, 2004
Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patientsRenzo Galanello, Lucia Perseu, Chiara Perra, et al.
Haematologica|August 10, 2012
Toward optimizing the use of deferasirox: potential benefits of combined use with deferoxamineRobert W Grady, Renzo Galanello, Rachel E Randolph, et al.
Acta Haematologica|November 13, 2013
α-globin gene quadruplication and heterozygous β-thalassemia: a not so rare cause of thalassemia intermediaRaffaella Origa, Maria Carla Sollaino, Caterina Borgna-Pignatti, et al.
Haematologica|January 18, 2015
Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermediaRaffaella Origa, Mario Cazzola, Elisabetta Mereu, et al.
Blood Cells, Molecules & Diseases|July 31, 2013
Complexity of the alpha-globin genotypes identified with thalassemia screening in SardiniaRaffaella Origa, Maria E Paglietti, Maria C Sollaino, et al.
European Journal of Internal Medicine|November 8, 2015
Development of a new disease severity scoring system for patients with non-transfusion-dependent thalassemiaM Domenica Cappellini, John B Porter, Khaled M Musallam, et al.
Haematologica|September 8, 2006
A prospective randomized controlled trial on the safety and efficacy of alternating deferoxamine and deferiprone in the treatment of iron overload in patients with thalassemiaRenzo Galanello, Antonis Kattamis, Antonio Piga, et al.
Human Gene Therapy|December 19, 2006
Therapeutic options for patients with severe beta-thalassemia: the need for globin gene therapyMichel Sadelain, Farid Boulad, Renzo Galanello, et al.
Pageof 12