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Journal Article
Nascimento, H., Vieira, E., Coimbra, S., Catarino, C., et al. (2016). Adipokine gene single-nucleotide polymorphisms in Portuguese obese adolescents: Associations with plasma concentrations of adiponectin, resistin, IL-6, IL-1β, and TNF-α. Childhood Obesity, 12(4), 300 - 313.
Costa, E., Rocha, S., Rocha-Pereira, P., Castro, E., et al. (2008). Altered erythrocyte membrane protein composition in chronic kidney disease stage 5 patients under haemodialysis and recombinant human erythropoietin therapy. Blood Purification, 26(3), 267 - 273.
Borges, A., Borges, M., Fernandes, J., Nascimento, H., et al. (2011). Apoptosis of peripheral CD4 ++ T-lymphocytes in end-stage renal disease patients under hemodialysis and rhEPO therapies. Renal Failure, 33(2), 138 - 143.
Rodrigues, C., Rocha, S., Nascimento, H., Vieira, E., et al. (2013). Bilirubin levels and redox status in a young healthy population. Acta Haematologica, 130(1), 57 - 60.
Do Sameiro-Faria, M., Ribeiro, S., Rocha-Pereira, P., Fernandes, J., et al. (2013). Body mass index and resistance to recombinant human erythropoietin therapy in maintenance hemodialysis patients. Renal Failure, 35(10), 1392 - 1398.
Teixeira, M., Rodrigues-Santos, P., Garrido, P., Costa, E., et al. (2012). Cardiac antiapoptotic and proproliferative effect of recombinant human erythropoietin in a moderate stage of chronic renal failure in the rat. Journal of Pharmacy and Bioallied Sciences, 4(1), 76 - 83.
Nascimento, H., Costa, E., Rocha-Pereira, P., Rego, C., et al. (2012). Cardiovascular risk factors in Portuguese obese children and adolescents: Impact of small reductions in body mass index imposed by lifestyle modifications. Open Biochemistry Journal, 6, 43 - 50.
Costa, E., Rocha, S., Rocha-Pereira, P., Castro, E., et al. (2008). Changes in red blood cells membrane protein composition during hemodialysis procedure. Renal Failure, 30(10), 971 - 975.
Kohlova, M., Ribeiro, S., Do Sameiro-Faria, M., Rocha-Pereira, P., et al. (2013). Circulating cell-free DNA levels in hemodialysis patients and its association with inflammation, iron metabolism, and rhEPO doses. Hemodialysis International, 17(4), 664 - 667.
Branca, R., Costa, E., Rocha, S., Coelho, H., et al. (2004). Coexistence of congenital red cell pyruvate kinase and band 3 deficiency. Clinical and Laboratory Haematology, 26(4), 297 - 300.
Ribeiro, S., Nascimento, H., Borges, A., Faria, M. D. S., et al. (2012). Comparison of Bio-Plex measurements with standard techniques. Clinical Chemistry and Laboratory Medicine, 50(2), 399 - 402.
Rocha, S., Costa, E., Rocha-Pereira, P., Ferreira, F., et al. (2011). Complementary markers for the clinical severity classification of hereditary spherocytosis in unsplenectomized patients. Blood Cells, Molecules, and Diseases, 46(2), 166 - 170.
Costa, E., Rocha, S., Rocha-Pereira, P., Castro, E., et al. (2008). Cross-talk between inflammation, coagulation/fibrinolysis and vascular access in hemodialysis patients. Journal of Vascular Access, 9(4), 248 - 253.
Costa, E., Rocha, S., Rocha-Pereira, P., Reis, F., et al. (2008). DMT1 (NRAMP2/DCT1) Genetic Variability and Resistance to Recombinant Human Erythropoietin Therapy in Chronic Kidney Disease Patients under Haemodialysis. Acta Haematologica, 120(1), 11 - 13.
Costa, E., Rocha, S., Rocha-Pereira, P., Reis, F., et al. (2009). Effect of hemodialysis procedure in prohepcidin serum levels in regular hemodialysis patients. Clinical Nephrology, 71(2), 233 - 235.
Rocha, S., Costa, E., Rocha-Pereira, P., Ferreira, F., et al. (2010). Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients. British Journal of Haematology, 149(5), 785 - 794.
Rocha, S., Costa, E., Rocha-Pereira, P., Ferreira, F., et al. (2011). Erythropoiesis versus inflammation in Hereditary Spherocytosis clinical outcome. Clinical Biochemistry, 44(13), 1137 - 1143.
Rocha, S., Costa, E., Catarino, C., Belo, L., et al. (2005). Erythropoietin levels in the different clinical forms of hereditary spherocytosis. British Journal of Haematology, 131(4), 534 - 542.
Costa, E., Swinkels, D. W., Laarakkers, C. M., Rocha-Pereira, P., et al. (2009). Hepcidin serum levels and resistance to recombinant human erythropoietin therapy in haemodialysis patients. Acta Haematologica, 122(4), 226 - 229.
Rocha, S., Costa, E., Ferreira, F., Cleto, E., et al. (2010). Hereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region-A comparison of the bilirubin plasmatic levels in the different clinical forms. Blood Cells, Molecules, and Diseases, 44(2), 117 - 119.
Costa, E., Lima, M., Rocha, S., Rocha-Pereira, P., et al. (2008). IL-7 serum levels and lymphopenia in hemodialysis patients, non-responders to recombinant human erythropoietin therapy. Blood Cells, Molecules, and Diseases, 41(1), 134 - 135.
Rodrigues, C., Vieira, E., Santos, R., de Carvalho, J., et al. (2012). Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects. Blood Cells, Molecules, and Diseases, 48(3), 166 - 172.
Costa, E., Lima, M., Alves, J. M., Rocha, S., et al. (2008). Inflammation, T-cell phenotype, and inflammatory cytokines in chronic kidney disease patients under hemodialysis and its relationship to resistance to recombinant human erythropoietin therapy. Journal of Clinical Immunology, 28(3), 268 - 275.
Rocha, S., Costa, E., Coimbra, S., Nascimento, H., et al. (2009). Linkage of cytosolic peroxiredoxin 2 to erythrocyte membrane imposed by hydrogen peroxide-induced oxidative stress. Blood Cells, Molecules, and Diseases, 43(1), 68 - 73.
Alexandre, N., Amorim, I., Caseiro, A. R., Pereira, T., et al. (2017). Long term performance evaluation of small-diameter vascular grafts based on polyvinyl alcohol hydrogel and dextran and MSCs-based therapies using the ovine pre-clinical animal model. International Journal of Pharmaceutics, 523(2), 515 - 530.

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