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Fernando F Costa

Showing results (1-10 of 154) with videos related to

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The Lancet. Haematology|August 21, 2022
Mitapivat for treatment of pyruvate kinase deficiencyFernando F Costa
Function (Oxford, England)|September 26, 2022
Sickle Cell Disease and Oxidative Stress: Implications for a Role of Diminished Endothelial SOD2 in Pulmonary ComplicationsNicola Conran, Fernando F Costa
Clinical Biochemistry|July 8, 2009
Hemoglobin disorders and endothelial cell interactionsNicola Conran, Fernando F Costa
Blood Cells, Molecules & Diseases|May 10, 2003
Mild hemolysis in a girl with G6PD Sumaré (class I variant) associated with G6PD A-Sara T O Saad, Fernando F Costa
International Journal of Molecular Sciences|April 13, 2023
Role of Macrophages in Sickle Cell Disease Erythrophagocytosis and ErythropoiesisRenata Sesti-Costa, Fernando F Costa, Nicola Conran
Hemoglobin|February 12, 2009
Newer aspects of the pathophysiology of sickle cell disease vaso-occlusionNicola Conran, Carla F Franco-Penteado, Fernando F Costa
Annals of Hematology|January 6, 2007
Leukocyte numbers correlate with plasma levels of granulocyte-macrophage colony-stimulating factor in sickle cell diseaseNicola Conran, Sara T O Saad, Fernando F Costa, et al.
Journal of Clinical Laboratory Analysis|August 22, 2018
Influence of alpha thalassemia on clinical and laboratory parameters among nigerian children with sickle cell anemiaOladele S Olatunya, Dulcineia M Albuquerque, Adekunle Adekile, et al.
American Journal of Hematology|July 30, 2004
Increased levels of soluble ICAM-1 in the plasma of sickle cell patients are reversed by hydroxyureaNicola Conran, André Fattori, Sara T O Saad, et al.
Hemoglobin|October 31, 2002
Alpha-thalassemia does not significantly contribute to the low MCV level of Hb C traitNadia M Silva, Cinira S Soledade, Fernando F Costa, et al.
Pageof 16

Showing results (1-10 of 154) with videos related to

Sort By:
Pageof 16
The Lancet. Haematology|August 21, 2022
Mitapivat for treatment of pyruvate kinase deficiencyFernando F Costa
Function (Oxford, England)|September 26, 2022
Sickle Cell Disease and Oxidative Stress: Implications for a Role of Diminished Endothelial SOD2 in Pulmonary ComplicationsNicola Conran, Fernando F Costa
Clinical Biochemistry|July 8, 2009
Hemoglobin disorders and endothelial cell interactionsNicola Conran, Fernando F Costa
Blood Cells, Molecules & Diseases|May 10, 2003
Mild hemolysis in a girl with G6PD Sumaré (class I variant) associated with G6PD A-Sara T O Saad, Fernando F Costa
International Journal of Molecular Sciences|April 13, 2023
Role of Macrophages in Sickle Cell Disease Erythrophagocytosis and ErythropoiesisRenata Sesti-Costa, Fernando F Costa, Nicola Conran
Hemoglobin|February 12, 2009
Newer aspects of the pathophysiology of sickle cell disease vaso-occlusionNicola Conran, Carla F Franco-Penteado, Fernando F Costa
Annals of Hematology|January 6, 2007
Leukocyte numbers correlate with plasma levels of granulocyte-macrophage colony-stimulating factor in sickle cell diseaseNicola Conran, Sara T O Saad, Fernando F Costa, et al.
Journal of Clinical Laboratory Analysis|August 22, 2018
Influence of alpha thalassemia on clinical and laboratory parameters among nigerian children with sickle cell anemiaOladele S Olatunya, Dulcineia M Albuquerque, Adekunle Adekile, et al.
American Journal of Hematology|July 30, 2004
Increased levels of soluble ICAM-1 in the plasma of sickle cell patients are reversed by hydroxyureaNicola Conran, André Fattori, Sara T O Saad, et al.
Hemoglobin|October 31, 2002
Alpha-thalassemia does not significantly contribute to the low MCV level of Hb C traitNadia M Silva, Cinira S Soledade, Fernando F Costa, et al.
Pageof 16