Browsing by Author Arruda, VR

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PreviewIssue DateTitleAuthor(s)AdvisorType
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
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
1999Spontaneous erythroid colony formation in Brazilian patients with sickle cell diseasePerlingeiro, RCR; Costa, FF; Saad, STO; Arruda, VR; Queiroz, MLS-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
2003Long-term hydroxyurea therapy in beta-thalassaemia patientsde Paula, EV; Lima, CSP; Arruda, VR; Alberto, FL; Saad, STO; Costa, FF-Artigo de periódico
1996Association of severe haemophilia A and factor V Leiden: Report of three casesArruda, VR; AnnichinoBizzacchi, JM; Antunes, SV; Costa, FF-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
2007A prospective study on the prevalence and risk factors for neonatal thrombocytopenia and platelet alloimmunization among 9332 unselected Brazilian newbornsCastro, V; Kroll, H; Origa, AF; Falconi, MA; Marques, SBD; Marba, ST; Passini, R; Annichino-Bizzacchi, JM; Costa, FF; Santoso, S; 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
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
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
1997Factor V Leiden is not common in children with portal vein thrombosisSeixas, CA; Hessel, G; Ribeiro, CC; Arruda, VR; AnnichinoBizzacchi, JM-Artigo de periódico
1998Genetic analysis of beta-thalassemia major and beta-thalassemia intermedia in BrazilFonseca, SF; Kerbauy, J; Escrivao, C; Figueiredo, MS; Cancado, R; Arruda, VR; Saad, STO; Costa, FF-Artigo de periódico
2004Genetic variability of platelet glycoprotein Ib alpha geneOzelo, MC; Costa, DSP; Siqueira, LH; Machado, TMF; Castro, V; Goncalves, MS; Menezes, RC; Soares, M; Annichino-Bizzacchi, JM; Costa, FF; Arruda, VR-Artigo de periódico
2006Evidence of multiyear factor IX expression by AAV-mediated gene transfer to skeletal muscle in an individual with severe hemophilia BJiang, HY; Pierce, GF; Ozelo, MC; de Paula, EV; Vargas, JA; Smith, P; Summer, J; Luk, A; Manno, CS; High, KA; Arruda, VR-Artigo de periódico
2000Possible association between cytomegalovirus infection and gastrointestinal bleeding in hemophiliac patientsNogueira, E; Arruda, VR; Bizzacchi, JMA; Costa, FF; Ozelo, MC; Rossi, CL; Costa, SCB-Artigo de periódico
1996Effect of alpha-thalassemia and beta-globin gene cluster haplotypes on the hematological and clinical features of sickle-cell anemia in BrazilFigueiredo, MS; Kerbauy, J; Goncalves, MS; Arruda, VR; Saad, STO; Sonati, MF; Stoming, T; Costa, FF-Artigo de periódico
1999Hb Rio Claro [beta 34(B16)Val -> Met]: a novel electrophoretically silent variant found in association with Hb Hasharon [alpha 47(CE5)Asp -> His] and alpha-thalassemia-2 (-alpha(3.7))Grignoli, CRE; Wenning, MRSC; Sonati, MF; Kimura, EM; Arruda, VR; Saad, STO; Costa, FF-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
1997G6PD sumare: A novel mutation in the G6PD gene (1292 T->G) associated with chronic nonspherocytic anemiaSaad, ST; Salles, TSI; Arruda, VR; Sonati, MF; Costa, FE-Artigo de periódico