Browsing by Author Kimura, EM

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PreviewIssue DateTitleAuthor(s)AdvisorType
2011Determination of beta(S) haplotypes in patients with sickle-cell anemia in the state of Rio Grande do Norte, BrazilCabral, CHK; Serafim, ESS; de Medeiros, WRDB; Fernandes, TAAD; Kimura, EM; Costa, FF; Sonati, MD; Rebecchi, IMM; de Medeiros, TMD-Artigo de periódico
1999Molecular characterization of hemoglobins Kurosaki [alpha 7 Lys -> Glu], G-Pest [alpha 74 Asp -> Asn], Stanleyville-II [alpha 78 Asn -> Lys] and J-Rovigo [alpha 53 Ala -> Asp]Wenning, MRSC; Kimura, EM; Jorge, SB; Costa, FF; Sonati, MF-Artigo de periódico
2003Thalassemia intermedia as a result of heterozygosis for beta(0)-thalassemia and alpha alpha alpha(anti-3.7)/alpha alpha genotype in a Brazilian patientKimura, EM; Grignoli, CRE; Pinheiro, VRP; Costa, FF; Sonati, MF-Artigo de periódico
2009Hb H disease resulting from the association of an alpha(0)-thalassemia allele [-(alpha)(20.5)] with an unstable alpha-globin variant [Hb Icaria]: First report on the occurrence in BrazilKimura, EM; Oliveira, DM; Fertrin, K; Pinheiro, VR; Jorge, SEDC; Costa, FF; Sonati, MD-Artigo de periódico
2006Hb Florida: A novel elongated C-terminal beta-globin variant causing dominant beta-thalassemia phenotypeWeinstein, BI; Erramouspe, B; Albuquerque, DM; Oliveira, DM; Kimura, EM; Costa, FF; Sonati, MF-Artigo de periódico
2007Hb Indianapolis [beta 112 (G14) Cys -> Arg] as the probable cause of moderate hemolytic anemia and renal damage in a Brazilian patientFattori, A; Kimura, EM; Albuquerque, DM; Oliveira, DM; Costa, FF; Sonati, MF-Artigo de periódico
1996Hb Camperdown [alpha(2)beta(2)104(G6)Arg->Ser] identified by DNA analysis in a Brazilian familyMiranda, SRP; Kimura, EM; Teixeira, RC; Bertuzzo, CS; Ramalho, AS; Saad, STO; Costa, FF-Artigo de periódico
2000Hb Campinas [alpha 26(B7)Ala -> Val]: a novel, electrophoretically silent, variantWenning, MRSC; Silva, NM; Jorge, SB; Kimura, EM; Costa, FF; Torsoni, MA; Ogo, SH; Sonati, MF-Artigo de periódico
2008Haptoglobin study in myasthenia gravisOliveira, LHM; Franca, MC; Nucci, A; de Oliveira, DM; Kimura, EM; Sonati, MD-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
2004Hb Osu-Christiansborg [beta 52(D3)Asp -> Asn): A de novo mutation in Brazilde Souza, LR; Kimura, EM; Albuquerque, DM; Costa, FF; Sonati, MD-Artigo de periódico
2004Structural alterations of the gamma-globin genes in a Brazilian populationDuarte, DF; Kimura, EM; Albuquerque, DM; Pinheiro, VRP; Costa, FF; Sonati, MDF-Artigo de periódico
2013A new beta(0)-thalassemia frameshift mutation [beta 48 (-T)] in a Uruguayan familyDa Luz, J; Lopez, P; Kimura, EM; Albuquerque, DM; Costa, FF; Sans, M; Sonati, MF-Artigo de periódico
1996Hereditary hemoglobinopathies in a population from southeast BrazilSonati, MF; Kimura, EM; Grotto, HZW; Gervasio, SA; Costa, FF-Artigo de periódico
2012Prevalence of alpha-thalassemia 3.7 kb deletion in the adult population of Rio Grande do Norte, BrazilAlcoforado, GHD; Bezerra, CM; Lemos, TMAM; de Oliveira, DM; Kimura, EM; Costa, FF; Sonati, MD; de Medeiros, TMD-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 patientWenning, MRSC; Harteveld, CL; Giordano, PC; Kimura, EM; Saad, STO; Costa, FF; Sonati, MF-Artigo de periódico
2002A novel beta-globin variant: Hb Pocos de Caldas [beta 61(E5)Lys -> Gln]Kimura, EM; Jorge, SB; Ogo, SH; Cesquini, M; Albuquerque, DM; Fattori, A; Saad, STO; Costa, FF; Sonati, MF-Artigo de periódico
1998Mild clinical expression of S-beta thalassemia in a Brazilian patient with the beta(+) IVS-I-6 (T -> C) mutationSonati, MD; Kaeda, J; Kimura, EM; Costa, FF; Luzzatto, L-Artigo de periódico
2009Two new unstable haemoglobins leading to chronic haemolytic anaemia: Hb Caruaru [beta 122 (GH5) Phe -> Ser], a probable case of germ line mutation, and Hb Olinda [beta 22 (B4)-25 (B7)], a deletion of a 12 base-pair sequenceBezerra, MAC; Albuquerque, DM; Santos, MNN; Kimura, EM; Jorge, SEDC; Oliveira, DM; Domingues, BLTB; Peres, JC; Araujo, AS; Costa, FF; Sonati, MF-Artigo de periódico
2010Beta-Globin Gene Cluster Haplotypes in Afro-Uruguayans from Two Geographical Regions (South and North)Da Luz, J; Kimura, EM; Costa, FF; Sonati, MD; Sans, M-Artigo de periódico