Browsing by Author Arruda, VR

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PreviewIssue DateTitleAuthor(s)AdvisorType
1999Spontaneous erythroid colony formation in Brazilian patients with sickle cell diseasePerlingeiro, RCR; Costa, FF; Saad, STO; Arruda, VR; Queiroz, MLS-Artigo de periódico
2006Successful transduction of liver in hemophilia by AAV-factor IX and limitations imposed by the host immune responseManno, CS; Arruda, VR; Pierce, GF; Glader, B; Ragni, M; Rasko, J; Ozelo, MC; Hoots, K; Blatt, P; Konkle, B; Dake, M; Kaye, R; Razavi, M; Zajko, A; Zehnder, J; Nakai, H; Chew, A; Leonard, D; Wright, JF; Lessard, RR; Sommer, JM; Tigges, M; Sabatino, D; Luk, A; Jiang, HY; Mingozzi, F; Couto, L; Ertl, HC; High, KA; Kay, MA-Artigo de periódico
1996Glutathione peroxidase, reduced glutathione, superoxide dismutase and catalase in red cells of patients with hairy cell leukemiaArruda, VR; Salles, TSI; Costa, FF; Saad, STO-Artigo de periódico
1998Geographic distribution of the 20210 G to A prothrombin variantRosendaal, FR; Doggen, CJM; Zivelin, A; Arruda, VR; Aiach, M; Siscovick, DS; Hillarp, A; Watzke, HH; Bernardi, F; Cumming, AM; Preston, FE; Reitsma, PH-Artigo de periódico
1999Hereditary hemorrhagic telangiectasia response to aminocaproic acid treatmentAnnichino-Bizzacchi, JM; Facchini, RM; Torresan, MZ; Arruda, VR-Artigo de periódico
1997The mutation Ala677->Val in the methylene tetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosisArruda, VR; vonZuben, PM; Chiaparini, LC; AnnichinoBizzacchi, JM; Costa, FF-Artigo de periódico
2004Follow-up of sickle cell disease patients with priapism treated by hydroxyureaSaad, STO; Lajolo, C; Gilli, S; Marques, JFC; Lima, CS; Costa, FF; Arruda, VR-Artigo de periódico
1998Prevalence of the mutation C677 -> T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in BrazilArruda, VR; Siqueira, LH; Goncalves, MS; von Zuben, PM; Soares, MCP; Menezes, R; Annichino-Bizzacchi, JM; Costa, FF-Artigo de periódico
1998Prevalence of the prothrombin gene variant 20210 G -> A among patients with myocardial infarctionArruda, VR; Siquiera, LH; Chiaparini, LC; Coelho, OR; Mansur, AP; Ramires, A; Annichino-Bizzacchi, JM-Artigo de periódico
1997Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial diseaseArruda, VR; AnnichinoBizzacchi, JM; Goncalves, MS; Costa, FF-Artigo de periódico
1998Prevalence of homozygosity for the deleted alleles of glutathione S-transferase mu (GSTM1) and theta (GSTT1) among distinct ethnic groups from Brazil: relevance to environmental carcinogenesis?Arruda, VR; Grignolli, CE; Goncalves, MS; Soares, MC; Menezes, R; Saad, STO; Costa, FF-Artigo de periódico
2003Prevalence of factor VII deficiency and molecular characterization of the F7 gene in Brazilian patientsRodrigues, DN; Siqueira, LH; Galizoni, AM; Arruda, VR; Annichino-Bizzacchi, JM-Artigo de periódico
2000The impact of the search for thrombophilia risk factors among antiphospholipid syndrome patients with thrombosisTorresan, M; Machado, TFGS; Siqueira, LH; Ozelo, MC; Arruda, VR; Annichino-Bizzacchi, JM-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
1996High-dose dexamethasone therapy in chronic idiopathic thrombocytopenic purpuraArruda, VR; AnnichinoBizzacchi, JM-Artigo de periódico
2000C282Y mutation in the HLA-H gene is not a risk factor for patients with myocardial infarctionAnnichino-Bizzacchi, JM; Saad, STO; Arruda, VR; Ramires, JAF; Siqueira, LH; Chiaparini, LC; Mansur, AP-Artigo de periódico
1999Frequencies of platelet-specific alloantigen systems 1-5 in three distinct ethnic groups in BrazilCastro, V; Origa, AF; Annichino-Bizzacchi, JM; Soares, M; Menezes, RC; Goncalves, MS; Costa, FF; Arruda, VR-Artigo de periódico
1999A novel splice site mutation in a Brazilian patient with hereditary antithrombin deficiency type IArnaldi, LAT; Polimeno, NC; Arruda, VR; Annichino-Bizzacchi, JM-Artigo de periódico
1999A novel nonsense mutation 6,E-X in the protein S gene causes type I deficiencyPugliese, L; Arruda, VR; Annichino-Bizzacchi, JM-Artigo de periódico
2001Antithrombin deficiency in Brazilian patients with venous thrombosis molecular characterization of a single splice site mutation, an insertion and a de novo point mutationArnaldi, LAT; Pretti, FA; Zampieri, JP; Ramos, CF; Arruda, VR; Annichino-Bizzacchi, JM-Artigo de periódico