Export 9 results:
Author Title [ Type(Desc)] Year
Filters: Author is Barbot, J.  [Clear All Filters]
Journal Article
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.
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.
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.
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.
Rocha, S., Vitorino, R. M. P., Lemos-Amado, F. M., Castro, E. B., et al. (2008). Presence of cytosolic peroxiredoxin 2 in the erythrocyte membrane of patients with hereditary spherocytosis. Blood Cells, Molecules, and Diseases, 41(1), 5 - 9.
Rocha, S., Rebelo, I., Costa, E., Catarino, C., et al. (2005). Protein deficiency balance as a predictor of clinical outcome in hereditary spherocytosis. European Journal of Haematology, 74(5), 374 - 380.
Pellegrino, R. M., Coutinho, M., D'Ascola, D., Lopes, A. M., et al. (2012). Two novel mutations in the tmprss6 gene associated with iron-refractory iron-deficiency anaemia (irida) and partial expression in the heterozygous form. British Journal of Haematology, 158(5), 668 - 672.

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