High levels of proinflammatory cytokines IL-6 and IL-8 are associated with a poor clinical outcome in sickle cell anemia von Domingos, Igor F., Pereira-Martins, Diego A., Sobreira, Marcondes J. V. C., Oliveira, Romulo T. D., Alagbe, Adekunle E., Lanaro, Carolina, Albuquerque, Dulcineia M., Blotta, Maria H. S. L., Araujo, Aderson S., Costa, Fernando F., Lucena-Araujo, Antonio R., Sonati, Maria F., Bezerra, Marcos A. C., Santos, Magnun N. N.

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Thalassemia major phenotype caused by HB Zürich‐Albisrieden [α2 59(E8) Gly > Arg (HBA2:C.178G > C)] in a Brazilian child von Pedroso, Gisele A., Kimura, Elza M., Santos, Magnun N.N., Albuquerque, Dulcinéia M., Malimpensa, Danaê, Jorge, Susan E., Verissimo, Monica P.A., Costa, Fernando F., Sonati, Maria F.

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Functional characterization of compound heterozygosity Hb S/Hb Deer Lodge in Brazil von Sobreira, Marcondes J., Batista, Thais H., Santana, Rodrigo M., Arcanjo, Gabriela S., Jorge, Susan E., Santos, Magnun N., Albuquerque, Dulcinéia M., Hatzlhofer, Betânia L., dos Anjos, Ana C., Costa, Fernando F., Araujo, Aderson S., Sonati, Maria F., Lucena-Araujo, Antonio R., Bezerra, Marcos A.

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PIP4KIIA and β‐globin: transcripts differentially expressed in reticulocytes and associated with high levels of Hb H in two siblings with Hb H disease von Wenning, Marcia R. S. C., Mello, Maricilda P., Andrade, Tiago G., Lanaro, Carolina, Albuquerque, Dulcineia M., Saad, Sara T. O., Costa, Fernando F., Sonati, Maria F.

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Two new unstable haemoglobins leading to chronic haemolytic anaemia: Hb Caruaru [β122 (GH5) Phe→Ser], a probable case of germ line mutation, and Hb Olinda [β22 (B4) ‐ 25 (B7)], a d... von Bezerra, Marcos A. C., Albuquerque, Dulcinéia M., Santos, Magnun N. N., Kimura, Elza M., Jorge, Susan E. D. C., Oliveira, Denise M., Domingues, Betânia L. T. B., Peres, Jaqueline C., Araújo, Aderson S., Costa, Fernando F., Sonati, Maria F.

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Haplotypes of α-globin gene regulatory element in two Brazilian native populations von Ribeiro, Daniela M., Figueiredo, Maria S., Costa, Fernando F., Sonati, Maria F.

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α-THALASSEMIA DOES NOT SIGNIFICANTLY CONTRIBUTE TO THE LOW MCV LEVEL OF Hb C TRAIT von Silva, Nadia M., Soledade, Cinira S., Costa, Fernando F., Sonati, Maria F.

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A NOVEL β-GLOBIN VARIANT: Hb POÇOS DE CALDAS [β61(E5)Lys→Gln] von Kimura, Elza M., Jorge, Simone B., Ogo, Satie H., Cesquini, Maristela, Albuquerque, Dulcineia M., Fattori, Andre, Saad, Sara T.O., Costa, Fernando F., Sonati, Maria F.

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Pipkiia and Beta-Globin: Transcripts Differentially Expressed in Reticulocytes and Associated with High Levels of Hb H in Two Siblings with Hb H Disease von Sonati, Maria F., Wenning, Marcia R., Mello, Maricilda P., Andrade, Tiago G., Lanaro, Carolina, Albuquerque, Dulcineia M., Titular, Sara Saad, Titular, Fernando F. Costa

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HbA Is More Effective Than HbF for Improving the Clinical Course in Sickle Cell Disease von Bezerra, Marcos A.C., Fattori, Andre, Santos, Magnum N., Albuquerque, Dulcineia M., Sonati, Maria F., Saad, Sara T.O., Araujo, Aderson S., Costa, Fernando F.

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Three Novel α-Globin Variants: Hb Itapira [α30(B11) Glu→Val (α1)], Hb Bom Jesus Da Lapa [α30(B11) Glu→Ala (α1)] and Hb Boa Esperança [α16(A14) Lis→Thr (α2)] von Sonati, Maria F., Kimura, Elza M., Albuquerque, Dulcineia M., Oliveira, Denise M., Costa, Fernando F.

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Three Novel α-Globin Variants: Hb Itapira [α30(B11) Glu→Val (α1)], Hb Bom Jesus Da Lapa [α30(B11) Glu→Ala (α1)] and Hb Boa Esperança [α16(A14) Lis→Thr (α2)] von Sonati, Maria F., Kimura, Elza M., Albuquerque, Dulcineia M., Oliveira, Denise M., Costa, Fernando F.

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HB Florida: A New Elongated C-Terminal β-Globin Variant Causing Dominant β-Thalassemia von Sonati, Maria F., Weinstein, Beatriz I., Erramouspe, Beatriz, Albuquerque, Dulcineia M., Kimura, Elza M., Oliveira, Denise M., Costa, Fernando F.

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PIP4KIIA and β-globin: transcripts differentially expressed in reticulocytes and associated with high levels of Hb H in two siblings with Hb H disease von Wenning, Marcia R. S. C., Mello, Maricilda P., Andrade, Tiago G., Lanaro, Carolina, Albuquerque, Dulcineia M., Saad, Sara T. O., Costa, Fernando F., Sonati, Maria F.

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Two new unstable haemoglobins leading to chronic haemolytic anaemia: Hb Caruaru [β122 (GH5) Phe→Ser], a probable case of germ line mutation, and Hb Olinda [β22 (B4) - 25 (B7)], a d... von Bezerra, Marcos A. C., Albuquerque, Dulcinéia M., Santos, Magnun N. N., Kimura, Elza M., Jorge, Susan E. D. C., Oliveira, Denise M., Domingues, Betânia L. T. B., Peres, Jaqueline C., Araújo, Aderson S., Costa, Fernando F., Sonati, Maria F.

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Beyond the Definitions of the Phenotypic Complications of Sickle Cell Disease : An Update on Management von Kesen, Muge R., Ballas, Samir K., Goldberg, Morton F., Lutty, Gerard A., Dampier, Carlton, Osunkwo, Ifeyinwa, Wang, Winfred C., Hoppe, Carolyn, Hagar, Ward, Darbari, Deepika S., Malik, Punam

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Functional Properties of Hb S and Hb C in Stored Cpda-1 Red Blood Cells Concentrate — a Prospective Study von Jorge, Susan Elisabeth, Grigoleto, Marcela Regina, Castro, Maria Lourdes Barjas, Costa, Fernando F., Sonati, Maria de Fátima

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The CCR5Δ32 Polymorphism in Brazilian Patients with Sickle Cell Disease von Costa, Fernando Ferreira, Sonati, M. F., Araújo, Aderson da Silva, Zaccariotto, Tânia Regina, Albuquerque, Dulcinéia Martins, Hatzlhofer, Betânia Lucena Domingues, Bezerra, Marcos André Cavalcanti, Faber, Eliel Wagner, Santos, Magnun Nueldo Nunes, Lopes, Mariana Pezzute, Ribeiro, Daniela Maria

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CRISPR/Cas9 Unsettle PIP4K2A and α, β, and γ Globin Genes Expression von Malimpensa, Danaê, Faber, Eliel, Corat, Marcus A.F., Lana, Marlous V.G., Strauss, Bryan E., Costa, Fernando F., Jorge, Susan Elisabeth, Sonati, Maria de Fátima

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Rare α0-thalassemia deletions detected by MLPA in five unrelated Brazilian patients von Mota, Natália O, Kimura, Elza M, Ferreira, Roberta D, Pedroso, Gisele A, Albuquerque, Dulcinéia M, Ribeiro, Daniela M, Santos, Magnun N N, Bittar, Cristina M, Costa, Fernando F, Sonati, Maria de Fatima

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