Percorrer por autor DE SOUSA, M.
Mostrar resultados 1-5 de 5.
Data | Título | Autor(es) | Tipo | Acesso |
Ago-2001 | Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload | PORTO, G.; CARDOSO, C.S.; GORDEUK, V.; CRUZ, E.; FRAGA, J.; AREIAS, J.; OLIVEIRA, J.C.; BRAVO, F.; GANGAIDZO, I.T.; MACPHAIL, A.P.; GOMO, Z.A.; MOYO, V.M.; MELO, G.; SILVA, C.; JUSTICA, B.; DE SOUSA, M. | article |  |
Nov-2005 | Low serum transferrin levels in HFE C282Y homozygous subjects are associated with low CD8(+) T lymphocyte numbers. | MACEDO, M.F.; CRUZ, E.; LACERDA, R.; PORTO, G.; DE SOUSA, M. | article |  |
Abr-1998 | Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA‐A29, and non‐classical forms of hemochromatosis. | PORTO, G.; ALVES, H.; RODRIGUES, P.; CABEDA, J.M.; PORTAL, C.; RUIVO, A.; JUSTICA, B.; WOLFF, R.; DE SOUSA, M. | article |  |
Abr-1999 | T cell numbers relate to bone involvement in Gaucher disease | LACERDA, L.; AROSA, F.A.; LACERDA, R.; CABEDA, J.; PORTO, G.; AMARAL, O.; FORTUNA, A.; PINTO, R.; OLIVEIRA, P.; MCLAREN, C.E.; SA MIRANDA, C.; DE SOUSA, M. | article |  |
Ago-2002 | Transferrin receptor 2 (TfR2) and HFE mutational analysis in non‐C282Y iron overload: identification of a novel TfR2 mutation | MATTMAN, A.; HUNTSMAN, D.; LOCKITCH, G.; LANGLOIS, S.; BUSKARD, N.; RALSTON, D.; BUTTERFIELD, Y.; RODRIGUES, P.; JONES, S.; PORTO, G.; MARRA, M.; DE SOUSA, M.; VATCHER, G. | article |  |