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PreviewIssue DateTitleAuthor(s)AdvisorType
2001The Agamma-195 (c-->g) Mutation In Hereditary Persistence Of Fetal Hemoglobin Is Not Associated With Activation Of A Reporter Gene In Vitro.Schreiber, R; Gonçalves, M S; Junqueira, M L; Saad, S T; Krieger, J E; Costa, F F-Artigo de periódico
2001Detection Of Somatic Mutations Of The Pig-a Gene In Brazilian Patients With Paroxysmal Nocturnal Hemoglobinuria.Franco De Carvalho, R; Arruda, V R; Saad, S T; Costa, F F-Artigo de periódico
1996Expression Of Spectrin Alpha I/65 Hereditary Elliptocytosis In Patients From Brazil.Pranke, P H; Basseres, D S; Costa, F F; Saad, S T-Artigo de periódico
1991Reduced Cortisol Secretion In Patients With Iron Deficiency.Saad, M J; Morais, S L; Saad, S T-Artigo de periódico
1992Glucose-6-phosphate Dehydrogenase Deficiency And Sickle Cell Disease In Brazil.Saad, S T; Costa, F F-Artigo de periódico
1996Glutathione Peroxidase, Reduced Glutathione, Superoxide Dismutase And Catalase In Red Cells Of Patients With Hairy Cell Leukemia.Arruda, V R; Salles, T S; Costa, F F; Saad, S T-Artigo de periódico
1998Haplotype Analysis And Agamma Gene Polymorphism Associated With The Brazilian Type Of Hereditary Persistence Of Fetal Hemoglobin.Bordin, S; Martins, J T; Gonçalves, M S; Melo, M B; Saad, S T; Costa, F F-Artigo de periódico
1998Prothrombin Mutant, Factor V Leiden, And Thermolabile Variant Of Methylenetetrahydrofolate Reductase Among Patients With Sickle Cell Disease In Brazil.Andrade, F L; Annichino-Bizzacchi, J M; Saad, S T; Costa, F F; Arruda, V R-Artigo de periódico
1997G6pd Sumaré: A Novel Mutation In The G6pd Gene (1292 T-->g) Associated With Chronic Nonspherocytic Anemia.Saad, S T; Salles, T S; Arruda, V R; Sonati, M F; Costa, F F-Artigo de periódico
1998Increased Tyrosine Phosphorylation Of Band 3 In Hemoglobinopathies.Terra, H T; Saad, M J; Carvalho, C R; Vicentin, D L; Costa, F F; Saad, S T-Artigo de periódico