Browsing by Author Saad, S T

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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
2001Hydroxyurea Promotes The Reduction Of Spontaneous Bfu-e To Normal Levels In Ss And S/beta Thalassemic Patients.Bincoletto, C; Perlingeiro, R C; Saad, S T; Costa, F F; Queiroz, M L-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
1990Acute Myocardial Infarction In Sickle Cell Anaemia Associated With Severe Hypoxia.Saad, S T; Arruda, V R; Junqueira, O O; Schelini, F A; Coelho, O B-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
-Molecular Characterization Of Glucose-6-phosphate Dehydrogenase Deficiency In Brazil.Saad, S T; Salles, T S; Carvalho, M H; Costa, F F-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
1998Autonomous Proliferation And Bcl-2 Expression Involving Haematopoietic Cells In Patients With Myelodysplastic Syndrome.Bincoletto, C; Saad, S T; Soares da Silva, E; Queiroz, M L-Artigo de periódico
1997Minimal Doses Of Hydroxyurea For Sickle Cell Disease.Lima, C S; Arruda, V R; Costa, F F; Saad, S T-Artigo de periódico
1998Presence Of Allele Alphalely In An Amazonian Indian Population.Bassères, D S; Salles, T S; Costa, F F; Saad, S T-Artigo de periódico
1998Expression Of Spectrin Alphai/50 Hereditary Elliptocytosis And Its Association With The Alphalely Allele.Bassères, D S; Pranke, P H; Vicentim, D; Costa, F F; Saad, S T-Artigo de periódico
1998Abnormal Antioxidant System In Erythrocytes Of Mercury-exposed Workers.Queiroz, M L; Pena, S C; Salles, T S; de Capitani, E M; Saad, S T-Artigo de periódico
1998Molecular Analysis Of The Retinoblastoma (rb1) Gene In Acute Myeloid Leukemia Patients.Melo, M B; Costa, F F; Saad, S T; Lorand-Metze, I; Bordin, S; Ahmad, N N-Artigo de periódico
1997Beta-spectrin Campinas: A Novel Shortened Beta-chain Variant Associated With Skipping Of Exon 30 And Hereditary Elliptocytosis.Basserès, D S; Pranke, P H; Sales, T S; Costa, F F; Saad, S T-Artigo de periódico
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