Browsing by Author Costa, FF

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PreviewIssue DateTitleAuthor(s)AdvisorType
2009New mutations detected by denaturing high performance liquid chromatography during screening of exon 6 bcr-abl mutations in patients with chronic myeloid leukemia treated with tyrosine kinase inhibitorsMascarenhas, CC; Cunha, AF; Miranda, EC; Zulli, R; Silveira, RA; Costa, FF; Pagnano, KBB; De Souza, CA-Artigo de periódico
1996The release of nitric oxide and superoxide anion by neutrophils and mononuclear cells from patients with sickle cell anaemiaDiasDaMotta, PM; Arruda, VR; Muscara, MN; Saad, STO; DeNucci, G; Costa, FF; CondinoNeto, A-Artigo de periódico
1998The relationship of bone marrow histology with the molecular pattern in chronic myeloid leukemiaVigorito, AC; Lorand-Metze, I; Chauffaile, MD; Costa, FF; Saad, STO-Artigo de periódico
1999Spontaneous erythroid colony formation in Brazilian patients with sickle cell diseasePerlingeiro, RCR; Costa, FF; Saad, STO; Arruda, VR; Queiroz, MLS-Artigo de periódico
2003Simple fluorescent PCR method for detection of large deletions in the beta-globin gene clusterDe Andrade, TG; Saad, STO; Sonati, MD; Costa, FF-Artigo de periódico
2009Constitutive JunB expression, associated with the JAK2 V617F mutation, stimulates proliferation of the erythroid lineageMonte-Mor, BDR; Plo, I; da Cunha, AF; Costa, GGL; de Albuquerque, DM; Jedidi, A; Villeval, JL; Badaoui, S; Lorand-Metze, I; Pagnano, KBB; Saad, STO; Vainchenker, W; Costa, FF-Artigo de periódico
2003Mild hemolysis in a girl with G6PD Sumare (class I variant) associated with G6PD A-Saad, STO; Costa, FF-Artigo de periódico
1998Mild clinical expression of S-beta thalassemia in a Brazilian patient with the beta(+) IVS-I-6 (T -> C) mutationSonati, MD; Kaeda, J; Kimura, EM; Costa, FF; Luzzatto, L-Artigo de periódico
2007Chronic liver abnormalities in sickle cell disease: A clinicopathological study in 70 living patientsTraina, F; Jorge, SG; Yamanaka, A; de Meirelles, LR; Costa, FF; Saad, STO-Artigo de periódico
2010Clinical and genetic risk factors for moderate hyperbilirubinemia in Brazilian newborn infantsMezzacappa, MA; Facchini, FP; Pinto, AC; Cassone, AEL; Souza, DS; Bezerra, MAC; Albuquerque, DM; Saad, STO; Costa, FF-Artigo de periódico
2004A novel FY allele in BraziliansCastilho, L; Rios, M; Pellegrino, J; Saad, STO; Costa, FF; Reid, ME-Artigo de periódico
2005A novel mutation in the GJA1 gene in a family with oculodentodigital dysplasiaVasconcellos, JPC; Melo, MB; Schimiti, RB; Bressanim, NC; Costa, FF; Costa, VP-Artigo de periódico
2009Two new unstable haemoglobins leading to chronic haemolytic anaemia: Hb Caruaru [beta 122 (GH5) Phe -> Ser], a probable case of germ line mutation, and Hb Olinda [beta 22 (B4)-25 (B7)], a deletion of a 12 base-pair sequenceBezerra, MAC; Albuquerque, DM; Santos, MNN; Kimura, EM; Jorge, SEDC; Oliveira, DM; Domingues, BLTB; Peres, JC; Araujo, AS; Costa, FF; Sonati, MF-Artigo de periódico
2003A possible role of the P53 gene deletion as a prognostic factor in multiple myelomaOrtega, MM; Melo, MB; De Souza, CA; Lorand-Metze, I; Costa, FF; Lima, CSP-Artigo de periódico
2003Long-term hydroxyurea therapy in beta-thalassaemia patientsde Paula, EV; Lima, CSP; Arruda, VR; Alberto, FL; Saad, STO; Costa, FF-Artigo de periódico
2001Low incidence of human herpesvirus 8 in bone marrow samples from Brazilian patients with multiple myelomaCunha, A; Costa, SC; Lima, CSP; Ortega, M; Costa, FF-Artigo de periódico
2002Liver transplantation in a patient with S beta degrees-thalassemiaGilli, SCO; Boin, IFS; Leonardi, LS; Luzo, ACM; Costa, FF; Saad, STO-Artigo de periódico
2008ARHGAP21 associates with FAK and PKC zeta and is redistributed after cardiac pressure overloadBorges, L; Bigarella, CL; Baratti, MO; Crosara-Alberto, DP; Joazeiro, PP; Franchini, KG; Costa, FF; Saad, STO-Artigo de periódico
2002ARHGAP10, a novel human gene coding for a potentially cytoskeletal Rho-GTPase activating proteinBasseres, DS; Tizzei, EV; Duarte, AAS; Costa, FF; Saad, STO-Artigo de periódico
2000Association of the alpha-spectrin R28H mutation with allele alpha(LELY) and with alpha I/alpha II domain haplotypes in three Brazilian familiesBasseres, DS; Bordin, S; Costa, FF; Saad, STO-Artigo de periódico