Browsing by Author Sonati, MF

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PreviewIssue DateTitleAuthor(s)AdvisorType
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
2004A transcript finishing initiative for closing gaps in the human transcriptomeSogayar, MC; Camargo, AA; Bettoni, F; Carraro, DM; Pires, LC; Parmigiani, MB; Ferreira, EN; Moreira, ES; Latorre, MRDO; Simpson, AJG; Cruz, LO; Degaki, TL; Festa, F; Massirer, KB; Camargo, F; Camargo, LP; Cunha, MAV; De Souza, SJ; Faria, M; Giuliatti, S; Kopp; Oliviera, PSL; Paiva, PB; Pereira, AA; Pinheiro, DG; Puga, RD; Souza, JES; Albuquerque, DM; Andrade, LEC; Baia, GS; Briones, MRS; Cavaleiro-Luna, AMS; Cerutti, JM; Costa, FF; Constanzi-Strauss, E; Espreafico, EM; Ferrasi, AC; Ferro, ES; Fortes, MAHZ; Furchi, JRF; Gianella-Neto, D; Goldman, GH; Goldman, MHS; Gruber, A; Guimaraes, GS; Hackel, C; Henrique-Silva, F; Kimura, ET; Leoni, SG; Macedo, C; Malnic, B; Manzini, CV; Marie, SKN; Martinez-Rossi, NM; Menossi, M; Miracca, EC; Nagai, MA; Nobrega, FG; Nobrega, MP; Oba-Shinjo, SM; Oliviera, MK; Orabona, GM; Otsuke, AY; Paco-Larson, ML; Paixao, BMC; Pandolfi, JRC; Pardini, MIMC; Passos-Bueno, MR; Passos, GAS; Pesquero, JB; Pessoa, JG; Rahal, P; Rainho, CA; Reis, CP; Ricca, TI; Rodriguez, V; Rogatto, SR; Romano, CM; Romeiro, JG; Rossi, A; Sa, RG; Sales, MM; SantAnna, SC; Santarosa, PL; Segato, F; Silva, WA; Silva, IDCG; Silva, NP; Soares-Costa, A; Sonati, MF; Strauss, BE; Tajara, EH; Valentini, SR; Villanova, FE; Ward, LS; Zanette, DL-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
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
2008Regulation of human alpha-globin gene expression and alpha-thalassemiaRibeiro, DM; Sonati, MF-Artigo de periódico
2012Expression profiles of phosphatidylinositol phosphate kinase genes during normal human in vitro erythropoiesisZaccariotto, TR; Lanaro, C; Albuquerque, DM; Santos, MNN; Bezerra, MAC; Cunha, FGP; Lorand-Metze, I; Araujo, AS; Costa, FF; Sonati, MF-Artigo de periódico
2009Influence of the polymorphisms of the alpha-major regulatory element HS-40 on in vitro gene expressionRibeiro, DM; Zaccariotto, TR; Santos, MNN; Costa, FF; Sonati, MF-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
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
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
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
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
2003Haplotypes of alpha-globin gene regulatory element in two Brazilian native populationsRibeiro, DM; Figueiredo, MS; Costa, FF; Sonati, MF-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
1996Hereditary hemoglobinopathies in a population from southeast BrazilSonati, MF; Kimura, EM; Grotto, HZW; Gervasio, SA; Costa, FF-Artigo de periódico
1997Hematological phenotype and the type of beta thalassemia mutation in BrazilBertuzzo, CS; Sonati, MF; Costa, FF-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
2006Reticulocyte evaluation in alpha(+)-thalassemiaKrugner, F; Zaccariotto, TR; Rosim, ET; Costa, FF; Grotto, HZW; Sonati, MF-Artigo de periódico
2002alpha-thalassemia does not significantly contribute to the low MCV level of Hb C traitSilva, NM; Soledade, CS; 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