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S T Saad

Showing results (51-60 of 91) with videos related to

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British Journal of Haematology|February 13, 2001
A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosisP G Gallagher, J D Ferreira, F F Costa, et al.
British Journal of Haematology|October 1, 1994
Red cell membrane protein abnormalities in hereditary spherocytosis in BrazilS T Saad, F F Costa, D L Vicentim, et al.
Sao Paulo Medical Journal = Revista Paulista De Medicina|September 1, 1996
Comparison of red cell distribution width and a red cell discriminant function incorporating volume dispersion for distinguishing iron deficiency from beta thalassemia trait in patients with microcytosisC S Lima, A R Reis, H Z Grotto, et al.
Clinical and Laboratory Haematology|May 3, 2000
Molecular heterogeneity of the A3 subgroupM L Barjas-Castro, M H Carvalho, M F Locatelli, et al.
Human Mutation|January 1, 1997
G6PD sumaré: a novel mutation in the G6PD gene (1292 T-->G) associated with chronic nonspherocytic anemiaS T Saad, T S Salles, V R Arruda, et al.
Human & Experimental Toxicology|June 9, 1998
Abnormal antioxidant system in erythrocytes of mercury-exposed workersM L Queiroz, S C Pena, T S Salles, et al.
American Journal of Hematology|September 2, 1998
Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in BrazilF L Andrade, J M Annichino-Bizzacchi, S T Saad, et al.
Leukemia & Lymphoma|January 1, 1997
N-ras gene point mutations in Brazilian acute myelogenous leukemia patients correlate with a poor prognosisM B De Melo, I Lorand-Metze, C S Lima, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|April 4, 2001
The Agamma-195 (C-->G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitroR Schreiber, M S Gonçalves, M L Junqueira, et al.
Acta Oncologica (Stockholm, Sweden)|January 1, 1997
Relationship between the type of BCR-ABL rearrangement and bone marrow histopathological features in chronic myeloid leukemiaG W Colleoni, M R Silva, R S Silva, et al.
Pageof 10

Showing results (51-60 of 91) with videos related to

Sort By:
Pageof 10
British Journal of Haematology|February 13, 2001
A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosisP G Gallagher, J D Ferreira, F F Costa, et al.
British Journal of Haematology|October 1, 1994
Red cell membrane protein abnormalities in hereditary spherocytosis in BrazilS T Saad, F F Costa, D L Vicentim, et al.
Sao Paulo Medical Journal = Revista Paulista De Medicina|September 1, 1996
Comparison of red cell distribution width and a red cell discriminant function incorporating volume dispersion for distinguishing iron deficiency from beta thalassemia trait in patients with microcytosisC S Lima, A R Reis, H Z Grotto, et al.
Clinical and Laboratory Haematology|May 3, 2000
Molecular heterogeneity of the A3 subgroupM L Barjas-Castro, M H Carvalho, M F Locatelli, et al.
Human Mutation|January 1, 1997
G6PD sumaré: a novel mutation in the G6PD gene (1292 T-->G) associated with chronic nonspherocytic anemiaS T Saad, T S Salles, V R Arruda, et al.
Human & Experimental Toxicology|June 9, 1998
Abnormal antioxidant system in erythrocytes of mercury-exposed workersM L Queiroz, S C Pena, T S Salles, et al.
American Journal of Hematology|September 2, 1998
Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in BrazilF L Andrade, J M Annichino-Bizzacchi, S T Saad, et al.
Leukemia & Lymphoma|January 1, 1997
N-ras gene point mutations in Brazilian acute myelogenous leukemia patients correlate with a poor prognosisM B De Melo, I Lorand-Metze, C S Lima, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|April 4, 2001
The Agamma-195 (C-->G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitroR Schreiber, M S Gonçalves, M L Junqueira, et al.
Acta Oncologica (Stockholm, Sweden)|January 1, 1997
Relationship between the type of BCR-ABL rearrangement and bone marrow histopathological features in chronic myeloid leukemiaG W Colleoni, M R Silva, R S Silva, et al.
Pageof 10