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Author Title [ Type(Asc)] Year
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Journal Article
Sims, A. - M., Timms, A. E., Bruges-Armas, J., Burgos-Vargas, R., et al. (2008). Prospective meta-analysis of interleukin 1 gene complex polymorphisms confirms associations with ankylosing spondylitis. Annals of the Rheumatic Diseases, 67(9), 1305 - 1309.
Couto, A. R., Bruges-Armas, J., Peach, C. A., Chapman, K., et al. (2007). A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis. Calcified Tissue International, 81(2), 81 - 84.
Gruber, B. L., Couto, A. R., Armas, J. B., Brown, M. A., et al. (2012). Novel ANKH amino terminus mutation (Pro5Ser) associated with early-onset calcium pyrophosphate disease with associated phosphaturia. Journal of Clinical Rheumatology, 18(4), 192 - 195.
Couto, A. R., Zhang, Y., Timms, A., Bruges-Armas, J., et al. (2012). Investigating ANKH and ENPP1 in Slovakian families with chondrocalcinosis. Rheumatology International, 32(9), 2745 - 2751.
Evans, D. M., Spencer, C. C. A., Pointon, J. J., Su, Z., et al. (2011). Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. Nature Genetics, 43(8), 761 - 767.
Couto, A. R., & Brown, M. A. (2007). Genetic factors in the pathogenesis of CPPD crystal deposition disease. Current Rheumatology Reports, 9(3), 231 - 236.

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