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Haematologica
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July 5, 2006
Randomized phase II trial of deferasirox (Exjade, ICL670), a once-daily, orally-administered iron chelator, in comparison to deferoxamine in thalassemia patients with transfusional iron overload
Antonio Piga, Renzo Galanello, Gian Luca Forni, et al.
Journal of Clinical Medicine
|
February 13, 2025
Thalassemias and Sickle Cell Diseases in Pregnancy: SITE Good Practice
Valeria Maria Pinto, Rosanna Cima, Rosario Di Maggio, et al.
Blood Transfusion = Trasfusione Del Sangue
|
November 16, 2020
Changing patterns of thalassaemia in Italy: a WebThal perspective
Filomena Longo, Paola Corrieri, Raffaella Origa, et al.
Blood
|
January 5, 2022
Mortality in β-thalassemia patients with confirmed pulmonary arterial hypertension on right heart catheterization
Valeria Maria Pinto, Khaled M Musallam, Giorgio Derchi, et al.
Haematologica
|
March 3, 2022
Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-thalassemia
Giorgio Derchi, Khaled M Musallam, Valeria Maria Pinto, et al.
American Journal of Hematology
|
September 21, 2017
Treatment of hepatitis C virus infection with direct-acting antiviral drugs is safe and effective in patients with hemoglobinopathies
Raffaella Origa, Maria Laura Ponti, Aldo Filosa, et al.
Blood Advances
|
January 22, 2026
Atrial fibrillation prevalence and its management in aging transfusion-dependent thalassemia patients: the FATHAL study
Valeria Di Stefano, Barbara Gianesin, Valeria Orecchia, et al.
Cancer
|
March 14, 2023
Reply to "Hepatocellular carcinoma in thalassemia and other hemoglobinopathies"
Raffaella Origa, Barbara Gianesin, Filomena Longo, et al.
Haematologica
|
October 20, 2018
Sotatercept, a novel transforming growth factor β ligand trap, improves anemia in β-thalassemia: a phase II, open-label, dose-finding study
Maria Domenica Cappellini, John Porter, Raffaella Origa, et al.
Haematologica
|
December 7, 2014
A genetic score for the prediction of beta-thalassemia severity
Fabrice Danjou, Marcella Francavilla, Franco Anni, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 93) with videos related to
Sort By:
Page
of 10
Haematologica
|
July 5, 2006
Randomized phase II trial of deferasirox (Exjade, ICL670), a once-daily, orally-administered iron chelator, in comparison to deferoxamine in thalassemia patients with transfusional iron overload
Antonio Piga, Renzo Galanello, Gian Luca Forni, et al.
Journal of Clinical Medicine
|
February 13, 2025
Thalassemias and Sickle Cell Diseases in Pregnancy: SITE Good Practice
Valeria Maria Pinto, Rosanna Cima, Rosario Di Maggio, et al.
Blood Transfusion = Trasfusione Del Sangue
|
November 16, 2020
Changing patterns of thalassaemia in Italy: a WebThal perspective
Filomena Longo, Paola Corrieri, Raffaella Origa, et al.
Blood
|
January 5, 2022
Mortality in β-thalassemia patients with confirmed pulmonary arterial hypertension on right heart catheterization
Valeria Maria Pinto, Khaled M Musallam, Giorgio Derchi, et al.
Haematologica
|
March 3, 2022
Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-thalassemia
Giorgio Derchi, Khaled M Musallam, Valeria Maria Pinto, et al.
American Journal of Hematology
|
September 21, 2017
Treatment of hepatitis C virus infection with direct-acting antiviral drugs is safe and effective in patients with hemoglobinopathies
Raffaella Origa, Maria Laura Ponti, Aldo Filosa, et al.
Blood Advances
|
January 22, 2026
Atrial fibrillation prevalence and its management in aging transfusion-dependent thalassemia patients: the FATHAL study
Valeria Di Stefano, Barbara Gianesin, Valeria Orecchia, et al.
Cancer
|
March 14, 2023
Reply to "Hepatocellular carcinoma in thalassemia and other hemoglobinopathies"
Raffaella Origa, Barbara Gianesin, Filomena Longo, et al.
Haematologica
|
October 20, 2018
Sotatercept, a novel transforming growth factor β ligand trap, improves anemia in β-thalassemia: a phase II, open-label, dose-finding study
Maria Domenica Cappellini, John Porter, Raffaella Origa, et al.
Haematologica
|
December 7, 2014
A genetic score for the prediction of beta-thalassemia severity
Fabrice Danjou, Marcella Francavilla, Franco Anni, et al.
Page
of 10