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Reticulocyte parameters and hemoglobin F production in sickle cell disease patients undergoing hydroxyurea therapy
(Wiley-lissNew YorkEUA, 2003)
Cytokine profiles in sickle cell anemia: Pathways to be unraveled
(Scientific Research Publishing, 2016)
Increased concentrations of IL-18 and uric acid in sickle cell anemia: Contribution of hemolysis, endothelial activation and the inflammasome
(2011)
Sickle cell anemia (SCA) is a common, severe monogenetic disorder characterized by chronic hemolysis, frequent infections, a chronic inflammatory state and recurrent occlusions of the microcirculation, resulting in painful ...
Increased concentrations of IL-18 and uric acid in sickle cell anemia: Contribution of hemolysis, endothelial activation and the inflammasome
(2011)
Sickle cell anemia (SCA) is a common, severe monogenetic disorder characterized by chronic hemolysis, frequent infections, a chronic inflammatory state and recurrent occlusions of the microcirculation, result-
ing in painful ...
UHPLC Quantitation Method and In vitro Studies of Two New Phthalimide Derivatives Planned to Treat Sickle Cell Disease
(Bentham Science Publ Ltd, 2017-01-01)
Background: Sickle cell disease is characterized by the occurrence of acute disability and progressive organ damage, and it is one of the most common and severe monogenic disorders around the world. Since hydroxycarbamide ...
Systemic lupus erythematosus in patients with sickle cell disease
(SpringerNew YorkEUA, 2008)