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Renzo Galanello

Showing results (61-70 of 113) with videos related to

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Annals of the New York Academy of Sciences|August 18, 2010
Strategy for a multicenter phase I clinical trial to evaluate globin gene transfer in beta-thalassemiaMichel Sadelain, Isabelle Rivière, Xiuyan Wang, et al.
Blood Cells, Molecules & Diseases|June 18, 2002
In vitro mass production of human erythroid cells from the blood of normal donors and of thalassemic patientsGiovanni Migliaccio, Roberta Di Pietro, Viviana di Giacomo, et al.
Blood|August 9, 2011
KLF1 gene mutations cause borderline HbA(2)Lucia Perseu, Stefania Satta, Paolo Moi, et al.
ISRN Hematology|November 16, 2011
Structural and Functional Characterization of a New Double Variant Haemoglobin (HbG-Philadelphia/Duarte α(2)β(2))Antonella Fais, Mariano Casu, Paolo Ruggerone, et al.
Haematologica|January 29, 2011
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrinStefania Satta, Lucia Perseu, Paolo Moi, et al.
European Journal of Haematology|November 22, 2008
Cholelithiasis in thalassemia majorRaffaella Origa, Renzo Galanello, Lucia Perseu, et al.
Blood|September 24, 2005
Seasonal variation of pretransfusion hemoglobin levels in patients with thalassemia majorCaterina Borgna-Pignatti, Mariela Ventola, David Friedman, et al.
European Journal of Haematology|February 19, 2013
Natural history of hepatitis C in thalassemia major: a long-term prospective studyMaria E Lai, Raffaella Origa, Fabrice Danjou, et al.
Blood|August 15, 2002
Lack of progressive hepatic fibrosis during long-term therapy with deferiprone in subjects with transfusion-dependent beta-thalassemiaIan R Wanless, George Sweeney, Amar P Dhillon, et al.
British Journal of Haematology|September 17, 2013
Impact of heart magnetic resonance imaging on chelation choices, compliance with treatment and risk of heart disease in patients with thalassaemia majorRaffaella Origa, Fabrice Danjou, Stefano Cossa, et al.
Pageof 12

Showing results (61-70 of 113) with videos related to

Sort By:
Pageof 12
Annals of the New York Academy of Sciences|August 18, 2010
Strategy for a multicenter phase I clinical trial to evaluate globin gene transfer in beta-thalassemiaMichel Sadelain, Isabelle Rivière, Xiuyan Wang, et al.
Blood Cells, Molecules & Diseases|June 18, 2002
In vitro mass production of human erythroid cells from the blood of normal donors and of thalassemic patientsGiovanni Migliaccio, Roberta Di Pietro, Viviana di Giacomo, et al.
Blood|August 9, 2011
KLF1 gene mutations cause borderline HbA(2)Lucia Perseu, Stefania Satta, Paolo Moi, et al.
ISRN Hematology|November 16, 2011
Structural and Functional Characterization of a New Double Variant Haemoglobin (HbG-Philadelphia/Duarte α(2)β(2))Antonella Fais, Mariano Casu, Paolo Ruggerone, et al.
Haematologica|January 29, 2011
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrinStefania Satta, Lucia Perseu, Paolo Moi, et al.
European Journal of Haematology|November 22, 2008
Cholelithiasis in thalassemia majorRaffaella Origa, Renzo Galanello, Lucia Perseu, et al.
Blood|September 24, 2005
Seasonal variation of pretransfusion hemoglobin levels in patients with thalassemia majorCaterina Borgna-Pignatti, Mariela Ventola, David Friedman, et al.
European Journal of Haematology|February 19, 2013
Natural history of hepatitis C in thalassemia major: a long-term prospective studyMaria E Lai, Raffaella Origa, Fabrice Danjou, et al.
Blood|August 15, 2002
Lack of progressive hepatic fibrosis during long-term therapy with deferiprone in subjects with transfusion-dependent beta-thalassemiaIan R Wanless, George Sweeney, Amar P Dhillon, et al.
British Journal of Haematology|September 17, 2013
Impact of heart magnetic resonance imaging on chelation choices, compliance with treatment and risk of heart disease in patients with thalassaemia majorRaffaella Origa, Fabrice Danjou, Stefano Cossa, et al.
Pageof 12