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Haematologica
|
July 14, 2011
Two atypical forms of HbH disease in Sardinia
Maria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
Haematologica
|
April 17, 2008
Onset of cardiac iron loading in pediatric patients with thalassemia major
John C Wood, Raffaella Origa, Annalisa Agus, et al.
Haematologica
|
May 10, 2007
Liver iron concentrations and urinary hepcidin in beta-thalassemia
Raffaella Origa, Renzo Galanello, Tomas Ganz, et al.
Annals of the New York Academy of Sciences
|
August 18, 2010
Combined iron chelation therapy
Renzo Galanello, Annalisa Agus, Simona Campus, et al.
American Journal of Hematology
|
July 15, 2016
Deferiprone-induced agranulocytosis: 20 years of clinical observations
Fernando Tricta, Jack Uetrecht, Renzo Galanello, et al.
Hemoglobin
|
October 16, 2004
Hb Belfast [beta15(A12)Trp-->Arg]: definition of the clinical and hematological phenotype
Renzo Galanello, Lucia Perseu, Susanna Barella, et al.
Blood
|
September 25, 2010
Homozygous deletion of the major alpha-globin regulatory element (MCS-R2) responsible for a severe case of hemoglobin H disease
Maria Carla Sollaino, Maria Elisabetta Paglietti, Daniela Loi, et al.
Haematologica
|
October 2, 2009
Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia
Maria Carla Sollaino, Maria Elisabetta Paglietti, Lucia Perseu, et al.
Hemoglobin
|
March 21, 2012
First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child
Maria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
American Journal of Hematology
|
August 19, 2011
Changing patterns of splenectomy in transfusion-dependent thalassemia patients
Antonio Piga, Melania Serra, Filomena Longo, et al.
Page
of 12
Search research articles
Search
Showing results (31-40 of 113) with videos related to
Sort By:
Page
of 12
Haematologica
|
July 14, 2011
Two atypical forms of HbH disease in Sardinia
Maria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
Haematologica
|
April 17, 2008
Onset of cardiac iron loading in pediatric patients with thalassemia major
John C Wood, Raffaella Origa, Annalisa Agus, et al.
Haematologica
|
May 10, 2007
Liver iron concentrations and urinary hepcidin in beta-thalassemia
Raffaella Origa, Renzo Galanello, Tomas Ganz, et al.
Annals of the New York Academy of Sciences
|
August 18, 2010
Combined iron chelation therapy
Renzo Galanello, Annalisa Agus, Simona Campus, et al.
American Journal of Hematology
|
July 15, 2016
Deferiprone-induced agranulocytosis: 20 years of clinical observations
Fernando Tricta, Jack Uetrecht, Renzo Galanello, et al.
Hemoglobin
|
October 16, 2004
Hb Belfast [beta15(A12)Trp-->Arg]: definition of the clinical and hematological phenotype
Renzo Galanello, Lucia Perseu, Susanna Barella, et al.
Blood
|
September 25, 2010
Homozygous deletion of the major alpha-globin regulatory element (MCS-R2) responsible for a severe case of hemoglobin H disease
Maria Carla Sollaino, Maria Elisabetta Paglietti, Daniela Loi, et al.
Haematologica
|
October 2, 2009
Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia
Maria Carla Sollaino, Maria Elisabetta Paglietti, Lucia Perseu, et al.
Hemoglobin
|
March 21, 2012
First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child
Maria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
American Journal of Hematology
|
August 19, 2011
Changing patterns of splenectomy in transfusion-dependent thalassemia patients
Antonio Piga, Melania Serra, Filomena Longo, et al.
Page
of 12