Browsing by Author Costa, F F

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PreviewIssue DateTitleAuthor(s)AdvisorType
2009Altered Levels Of Cytokines And Inflammatory Mediators In Plasma And Leukocytes Of Sickle Cell Anemia Patients And Effects Of Hydroxyurea Therapy.Lanaro, C; Franco-Penteado, C F; Albuqueque, D M; Saad, S T O; Conran, N; Costa, F F-Artigo de periódico
2010High Frequency Of Vitamin B12 Deficiency In A Brazilian Population.Xavier, J M; Costa, F F; Annichino-Bizzacchi, J M; Saad, S T O-Artigo de periódico
2011Analysis Of The Workers Head Transcriptome Of The Asian Subterranean Termite, Coptotermes Gestroi.Leonardo, F C; da Cunha, A F; da Silva, M J; Carazzolle, M F; Costa-Leonardo, A M; Costa, F F; Pereira, G A-Artigo de periódico
2005High Frequency Of Partial Diiia And Dar Alleles Found In Sickle Cell Disease Patients Suggests Increased Risk Of Alloimmunization To Rhd.Castilho, L; Rios, M; Rodrigues, A; Pellegrino, J; Saad, S T O; Costa, F F-Artigo de periódico
2007Hb Indianapolis [beta112 (g14) Cys-->arg] As The Probable Cause Of Moderate Hemolytic Anemia And Renal Damage In A Brazilian Patient.Fattori, A; Kimura, E M; Albuquerque, D M; Oliveira, D M; Costa, F F; Sonati, M F-Artigo de periódico
2015Increased Circulating Pedf And Low Sicam-1 Are Associated With Sickle Cell Retinopathy.Cruz, P R S; Lira, R P C; Pereira Filho, S A C; Souza, B B; Mitsuushi, F N; Menaa, F; Fertrin, K Y; Vasconcellos, J P C; Conran, N; Costa, F F; Melo, M B-Artigo de periódico
2005Increasing Seroprevalence Of Human Herpesvirus 8 (hhv-8) With Age Confirms Hhv-8 Endemicity In Amazon Amerindians From Brazil.Cunha, A M G; Caterino-de-Araujo, A; Costa, S C B; Santos-Fortuna, E; Boa-Sorte, N C A; Gonçalves, M S; Costa, F F; Galvão-Castro, B-Artigo de periódico
2005Rhnull Syndrome: Identification Of A Novel Mutation In Rhce.Rosa, K A; Reid, M E; Lomas-Francis, C; Powell, V I; Costa, F F; Stinghen, S T; Watanabe, A M; Carboni, E K; Baldon, J P; Jucksch, M M F; Castilho, L-Artigo de periódico
2012Lack Of Association Between Mdm2 Snp309 And Tp53 Arg72pro Polymorphisms With Clinical Outcomes In Myelodysplastic Syndrome.Machado-Neto, J A; Traina, F; De Melo Campos, P; Andreoli-Risso, M F; Costa, F F; Olalla Saad, S T-Artigo de periódico
2007Three Novel Mutations In The Activin Receptor-like Kinase 1 (alk-1) Gene In Hereditary Hemorrhagic Telangiectasia Type 2 In Brazilian Patients.Assis, A M; Costa, F F; Arruda, V R; Annichino-Bizzacchi, J M; Bertuzzo, C S-Artigo de periódico
2007Early Proliferation Of Umbilical Cord Blood Cells From Premature Neonates.Luzo, A C M; Duarte, A S S; Salles, T S I; Queiroz, M L S; Lorand-Metze, I; Costa, F F; Saad, S T O-Artigo de periódico
2008Low Expression Of Apaf-1xl In Acute Myeloid Leukemia May Be Associated With The Failure Of Remission Induction Therapy.Benites, B D; Fattori, A; Hackel, C; Lorand-Metze, I; De Souza, C A; Schulz, E; Costa, F F; Saad, S T O-Artigo de periódico
2009Influence Of The Polymorphisms Of The Alpha-major Regulatory Element Hs-40 On In Vitro Gene Expression.Ribeiro, D M; Zaccariotto, T R; Santos, M N N; Costa, F F; Sonati, M F-Artigo de periódico
2006Reticulocyte Evaluation In Alpha(+)-thalassemia.Krügner, F; Zaccariotto, T R; Rosim, E T; Costa, F F; Grotto, H Z W; Sonati, M F-Artigo de periódico
2007Evaluation Of Reticulated Platelets In Patients With Sickle Cell Diseases.Noronha, J F A; Costa, F F; Saad, S T O; Lorand-Metze, I G H; Grotto, H Z W-Artigo de periódico
2010Clinical And Genetic Risk Factors For Moderate Hyperbilirubinemia In Brazilian Newborn Infants.Mezzacappa, M A; Facchini, F P; Pinto, A C; Cassone, A E L; Souza, D S; Bezerra, M A C; Albuquerque, D M; Saad, S T O; 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
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
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
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
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