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PreviewIssue DateTitleAuthor(s)AdvisorType
2010High Frequency Of Vitamin B12 Deficiency In A Brazilian Population.Xavier, J M; Costa, F F; Annichino-Bizzacchi, J M; Saad, S T O-Artigo de periódico
2007Hb Indianapolis [beta112 (g14) Cys-->arg] As The Probable Cause Of Moderate Hemolytic Anemia And Renal Damage In A Brazilian Patient.Fattori, A; Kimura, E M; Albuquerque, D M; Oliveira, D M; Costa, F F; Sonati, M F-Artigo de periódico
2007Three Novel Mutations In The Activin Receptor-like Kinase 1 (alk-1) Gene In Hereditary Hemorrhagic Telangiectasia Type 2 In Brazilian Patients.Assis, A M; Costa, F F; Arruda, V R; Annichino-Bizzacchi, J M; Bertuzzo, C S-Artigo de periódico
-Abo Blood Group In Amerindians From Brazilian Amazon.Barjas-Castro, M L; Soares, M C P; Menezes, R C; Carvalho, M H M; Costa, F F; Saad, S T O-Artigo de periódico
2011Characterization Of Alpha Thalassemic Genotypes By Multiplex Ligation-dependent Probe Amplification In The Brazilian Population.Suemasu, C N; Kimura, E M; Oliveira, D M; Bezerra, M A C; Araújo, A S; Costa, F F; Sonati, M F-Artigo de periódico
2002Molecular Identification Of Sicilian (deltabeta) Degrees-thalassemia Associated With Beta-thalassemia And Hemoglobin S In Andrade, T G; Fattori, A; Saad, S T O; Sonati, M F; Costa, F F-Artigo de periódico
2002Hemoglobin H Disease Resulting From The Association Of The - Alpha 3.7 Rightward Deletion And The (alpha Alpha)mm Deletion In A Brazilian Patient.Wenning, M R S C; Harteveld, C L; Giordano, P C; Kimura, E M; Saad, S T O; Costa, F F; Sonati, M F-Artigo de periódico
2001High Prevalence Of Alpha-thalassemia Among Individuals With Microcytosis And Hypochromia Without Anemia.Borges, E; Wenning, M R; Kimura, E M; Gervásio, S A; Costa, F F; Sonati, M F-Artigo de periódico
2001Detection Of Somatic Mutations Of The Pig-a Gene In Brazilian Patients With Paroxysmal Nocturnal Hemoglobinuria.Franco De Carvalho, R; Arruda, V R; Saad, S T; Costa, F F-Artigo de periódico
2002Presence Of The Rhd Pseudogene And The Hybrid Rhd-ce-d(s) Gene In Brazilians With The D-negative Phenotype.Rodrigues, A; Rios, M; Pellegrino, J; Costa, F F; Castilho, L-Artigo de periódico