Browsing by Author Costa, F F

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PreviewIssue DateTitleAuthor(s)AdvisorType
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
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
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
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
2004A Novel Fy Allele In Brazilians.Castilho, L; Rios, M; Pellegrino, J; Saad, S T O; Costa, F F; Reid, M E-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
1999Spontaneous Erythroid Colony Formation In Brazilian Patients With Sickle Cell Disease.Perlingeiro, R C; Costa, F F; Saad, S T; Arruda, V R; Queiroz, M L-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
1992Glucose-6-phosphate Dehydrogenase Deficiency And Sickle Cell Disease In Brazil.Saad, S T; Costa, F F-Artigo de periódico
1992The Ivs-i-110 (g-->t) And Codon 39 (c-->t) Beta-thalassemia Mutations In Association With Alpha-thal-2 (-3.7 Kb) And Hb Hasharon [alpha 47(ce5)asp-->his] In A Brazilian Patient.Costa, F F; Figueredo, M S; Sonati, M F; Kimura, E M; Martins, C S-Artigo de periódico
-[differentiation Between Heterozygotic Beta-thalassemia And Iron Deficiency Anemia].Sonati, M de F; Grotto, H Z; Kimura, E M; Costa, F F-Artigo de periódico
-[detection Of Hemophilia A Gene Carriers In A Brazilian Population].Arruda, V R; Annichino-Bizzacchi, J M; Costa, F F-Artigo de periódico
2000Possible Association Between Cytomegalovirus Infection And Gastrointestinal Bleeding In Hemophiliac Patients.Nogueira, E; Arruda, V R; Bizzacchi, J M; Costa, F F; Ozelo, M C; Rossi, C L; Costa, S C-Artigo de periódico
2003Screening For Mutations In Human Alpha-globin Genes By Nonradioactive Single-strand Conformation Polymorphism.Jorge, S B; Melo, M B; Costa, F F; Sonati, M F-Artigo de periódico
-Abo Blood Group In Amerindians From Brazilian Amazon.Barjas-Castro, M L; Soares, M C P; Menezes, R C; Carvalho, M H M; Costa, F F; Saad, S T O-Artigo de periódico
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
2004Weakened Expression Of 'e' Owing To Concomitant Occurrence Of Cys16 And Val245 (vs Antigen).Rodrigues, A; Rios, M; Costa, F F; Saad, S T O; Pellegrino, J; Castilho, L-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
2002Accuracy Of The Urinary Albumin To Creatinine Ratio As A Predictor Of Albuminuria In Adults With Sickle Cell Disease.Lima, C S P; Bottini, P V; Garlipp, C R; Santos, A O; Costa, F F; Saad, S T O-Artigo de periódico