Browsing by Author Arruda, VR

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PreviewIssue DateTitleAuthor(s)AdvisorType
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
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
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
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
2003Long-term hydroxyurea therapy in beta-thalassaemia patientsde Paula, EV; Lima, CSP; Arruda, VR; Alberto, FL; Saad, STO; 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
1998Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in BrazilAndrade, FL; Annichino-Bizzacchi, JM; Saad, STO; Costa, FF; Arruda, VR-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
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
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
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
1999Hereditary hemorrhagic telangiectasia response to aminocaproic acid treatmentAnnichino-Bizzacchi, JM; Facchini, RM; Torresan, MZ; Arruda, VR-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
1996High-dose dexamethasone therapy in chronic idiopathic thrombocytopenic purpuraArruda, VR; AnnichinoBizzacchi, JM-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 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