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PreviewIssue DateTitleAuthor(s)AdvisorType
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
2007Three novel mutations in the activin receptor-like kinase 1 (ALK-1) gene in hereditary hemorrhagic telangiectasia type 2 in Brazilian patientsAssis, AM; Costa, FF; Arruda, VR; Annichino-Bizzacchi, JM; Bertuzzo, CS-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
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
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
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