Export 8 results:
Author Title [ Type(Desc)] Year
Filters: Author is Almeida, S.  [Clear All Filters]
Journal Article
Correia, A. P., Pinto, J. P., Dias, V., Mascarenhas, C., et al. (2009). CAT53 and HFE alleles in Alzheimer's disease: A putative protective role of the C282Y HFE mutation. Neuroscience Letters, 457(3), 129 - 132.
Cruz, E., Melo, G., Lacerda, R., Almeida, S., & Porto, G. (2006). The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: An update of clinical and immunological data from 70 C282Y homozygous subjects. Blood Cells, Molecules, and Diseases, 37(1), 33 - 39.
Guiomar, R., S. da Silva, P., Conde, P., Cristóvão, P., et al. (2017). Cross-protection to new drifted influenza A(H3) viruses and prevalence of protective antibodies to seasonal influenza, during 2014 in Portugal. Vaccine, 35(16), 2092 - 2099.
Cardoso, C. S., Araújo, H. C., Cruz, E., Afonso, A., et al. (2006). Haemochromatosis gene (HFE) mutations in viral-associated neoplasia: Linkage to cervical cancer. Biochemical and Biophysical Research Communications, 341(1), 232 - 238.
Cruz, E., Vieira, J., Gonçalves, R., Alves, H., et al. (2004). Involvement of the Major Histocompatibility Complex region in the regulation regulation of circulating CD8+ T-cell numbers in humans. Tissue Antigens, 64(1), 25 - 34.
Beirão, I., Almeida, S., Swinkels, D., Costa, P. M. P., et al. (2008). Low serum levels of prohepcidin, but not hepcidin-25, are related to anemia in familial amyloidosis TTR V30M. Blood Cells, Molecules, and Diseases, 41(2), 175 - 178.
Vieira, J., Cardoso, C. S., Pinto, J., Patil, K., et al. (2007). A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans. International Journal of Immunogenetics, 34(5), 359 - 367.
Cruz, E., Vieira, J., Almeida, S., Lacerda, R., et al. (2006). A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: Relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload. BMC Medical Genetics, 7.

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