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S T Saad

Showing results (31-40 of 91) with videos related to

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The New England Journal of Medicine|March 27, 1997
Successful use of hydroxyurea in beta-thalassemia majorV R Arruda, C S Lima, S T Saad, et al.
European Journal of Haematology|January 26, 1999
Haematopoietic response and bcl-2 expression in patients with acute myeloid leukaemiaC Bincoletto, S T Saad, E S da Silva, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|May 30, 2001
Detection of somatic mutations of the PIG-A gene in Brazilian patients with paroxysmal nocturnal hemoglobinuriaR Franco De Carvalho, V R Arruda, S T Saad, et al.
The International Journal of Artificial Organs|June 1, 1995
Automated erythrocytapheresis in sickle cell anaemiaJ F Marques Júnior, S T Saad, F F Costa, et al.
Neoplasma|July 8, 2009
Variation of bone marrow CD34+ cell subsets in myelodysplastic syndromes according to who typesS C Reis, F Traina, K Metze, et al.
Hemoglobin|April 13, 2001
Hydroxyurea promotes the reduction of spontaneous BFU-e to normal levels in SS and S/beta thalassemic patientsC Bincoletto, R C Perlingeiro, S T Saad, et al.
British Journal of Haematology|November 13, 2001
beta-Spectrin S(ta) Bárbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicismD S Bassères, A S Duarte, H Hassoun, et al.
Biochemistry and Molecular Biology International|June 1, 1997
cDNA-derived amino-acid sequence of a land turtle (Geochelone carbonaria) beta-chain hemoglobinS Bordin, A N Meza, S T Saad, et al.
American Journal of Hematology|March 8, 2000
beta-thalassemia trait might increase the severity of hemochromatosis in subjects with the C282Y mutation in the HFE geneV R Arruda, M F Agostinho, R Cançado, et al.
Blood|February 7, 1998
Beta-spectrin Promiss-ao: a translation initiation codon mutation of the beta-spectrin gene (ATG --> GTG) associated with hereditary spherocytosis and spectrin deficiency in a Brazilian familyD S Bassères, D L Vicentim, F F Costa, et al.
Pageof 10

Showing results (31-40 of 91) with videos related to

Sort By:
Pageof 10
The New England Journal of Medicine|March 27, 1997
Successful use of hydroxyurea in beta-thalassemia majorV R Arruda, C S Lima, S T Saad, et al.
European Journal of Haematology|January 26, 1999
Haematopoietic response and bcl-2 expression in patients with acute myeloid leukaemiaC Bincoletto, S T Saad, E S da Silva, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|May 30, 2001
Detection of somatic mutations of the PIG-A gene in Brazilian patients with paroxysmal nocturnal hemoglobinuriaR Franco De Carvalho, V R Arruda, S T Saad, et al.
The International Journal of Artificial Organs|June 1, 1995
Automated erythrocytapheresis in sickle cell anaemiaJ F Marques Júnior, S T Saad, F F Costa, et al.
Neoplasma|July 8, 2009
Variation of bone marrow CD34+ cell subsets in myelodysplastic syndromes according to who typesS C Reis, F Traina, K Metze, et al.
Hemoglobin|April 13, 2001
Hydroxyurea promotes the reduction of spontaneous BFU-e to normal levels in SS and S/beta thalassemic patientsC Bincoletto, R C Perlingeiro, S T Saad, et al.
British Journal of Haematology|November 13, 2001
beta-Spectrin S(ta) Bárbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicismD S Bassères, A S Duarte, H Hassoun, et al.
Biochemistry and Molecular Biology International|June 1, 1997
cDNA-derived amino-acid sequence of a land turtle (Geochelone carbonaria) beta-chain hemoglobinS Bordin, A N Meza, S T Saad, et al.
American Journal of Hematology|March 8, 2000
beta-thalassemia trait might increase the severity of hemochromatosis in subjects with the C282Y mutation in the HFE geneV R Arruda, M F Agostinho, R Cançado, et al.
Blood|February 7, 1998
Beta-spectrin Promiss-ao: a translation initiation codon mutation of the beta-spectrin gene (ATG --> GTG) associated with hereditary spherocytosis and spectrin deficiency in a Brazilian familyD S Bassères, D L Vicentim, F F Costa, et al.
Pageof 10