Evaluation of the immature platelet fraction contribute to the differential diagnosis of hereditary, immune and other acquired thrombocytopenias by Ferreira, F. L. B., Colella, M. P., Medina, S. S., Costa-Lima, C., Fiusa, M. M. L., Costa, L. N. G., Orsi, F. A., Annichino-Bizzacchi, J. M., Fertrin, K. Y., Gilberti, M. F. P., Ozelo, M. C., De Paula, E. V.

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A chip calorimetry-based method for the real-time investigation of metabolic activity changes in human erythrocytes caused by cell sickling by Lerchner, J., Volpe, P. O. L., Lanaro, C., Fertrin, K. Y., Costa, F. F., Albuquerque, D. M., Haenschke, F., Mertens, F.

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Increased circulating PEDF and low sICAM-1 are associated with sickle cell retinopathy by Cruz, P.R.S., Lira, R.P.C., Pereira Filho, S.A.C., Souza, B.B., Mitsuushi, F.N., Menaa, F., Fertrin, K.Y., Vasconcellos, J.P.C., Conran, N., Costa, F.F., Melo, M.B.

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UDP-glucuronosyltransferase 1 gene promoter polymorphism is associated with increased serum bilirubin levels and cholecystectomy in patients with sickle cell anemia by Fertrin, K. Y., Melo, M. B., Assis, Â. M., Saad, S. T. O., Costa, F. F.

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A thalidomide–hydroxyurea hybrid increases HbF production in sickle cell mice and reduces the release of proinflammatory cytokines in cultured monocytes by Lanaro, Carolina, Franco-Penteado, Carla F., Silva, Fabio H., Fertrin, Kleber Y., dos Santos, Jean Leandro, Wade, Marlene, Yerigenahally, Shobha, de Melo, Thais R., Chin, Chung Man, Kutlar, Abdullah, Meiler, Steffen E., Costa, Fernando Ferreira

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