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Haematologica
|
October 14, 2003
Thalassemia minor, the Gilbert mutation, and the risk of gallstones
Caterina Borgna-Pignatti, Francesca Rigon, Luciano Merlo, et al.
Haematologica
|
November 12, 2009
Pregnancy and beta-thalassemia: an Italian multicenter experience
Raffaella 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 patients
Renzo Galanello, Lucia Perseu, Chiara Perra, et al.
Haematologica
|
August 10, 2012
Toward optimizing the use of deferasirox: potential benefits of combined use with deferoxamine
Robert 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 intermedia
Raffaella 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 intermedia
Raffaella 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 Sardinia
Raffaella 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 thalassemia
M 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 thalassemia
Renzo 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 therapy
Michel Sadelain, Farid Boulad, Renzo Galanello, et al.
Page
of 12
Search research articles
Search
Showing results (41-50 of 113) with videos related to
Sort By:
Page
of 12
Haematologica
|
October 14, 2003
Thalassemia minor, the Gilbert mutation, and the risk of gallstones
Caterina Borgna-Pignatti, Francesca Rigon, Luciano Merlo, et al.
Haematologica
|
November 12, 2009
Pregnancy and beta-thalassemia: an Italian multicenter experience
Raffaella 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 patients
Renzo Galanello, Lucia Perseu, Chiara Perra, et al.
Haematologica
|
August 10, 2012
Toward optimizing the use of deferasirox: potential benefits of combined use with deferoxamine
Robert 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 intermedia
Raffaella 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 intermedia
Raffaella 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 Sardinia
Raffaella 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 thalassemia
M 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 thalassemia
Renzo 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 therapy
Michel Sadelain, Farid Boulad, Renzo Galanello, et al.
Page
of 12