Export 9 results:
Author Title [ Type(Desc)] Year
Filters: Author is Beirão, I.  [Clear All Filters]
Journal Article
Lobato, L., Beirão, I., Silva, M., Fonseca, I., et al. (2004). End-stage renal disease and dialysis in hereditary amyloidosis TTR V30M: Presentation, survival and prognostic factors. Amyloid, 11(1), 27 - 37.
Beirão, I., Moreira, L., Barandela, T., Lobato, L., et al. (2010). Erythropoietin production by distal nephron in normal and familial amyloidotic adult human kidneys. Clinical Nephrology, 74(5), 327 - 335.
Beirão, J. M., Malheiro, J., Lemos, C., Matos, E., et al. (2015). Impact of liver transplantation on the natural history of oculopathy in Portuguese patients with transthyretin (V30M) amyloidosis. Amyloid, 22(1), 31 - 35.
Beirão, I., Lobato, L., Costa, P. M., Fonseca, I., et al. (2004). Kidney and anemia in familial amyloidosis type I. Kidney international, 66(5), 2004 - 2009.
Beirão, I., Lobato, L., Costa, P. M. P., Fonseca, I., et al. (2007). Liver transplantation and anemia in familial amyloidosis ATTR V30M. Amyloid, 14(1), 33 - 37.
Beirão, I., Moreira, L., Porto, G., Lobato, L., et al. (2008). Low erythropoietin production in familial amyloidosis TTR V30M is not related with renal congophilic amyloid deposition: A clinicopathologic study of twelve cases. Nephron - Clinical Practice, 109(2), c95 - c99.
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.
Balreira, A., Gaspar, P., Caiola, D., Chaves, J., et al. (2008). A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome. Human Molecular Genetics, 17(14), 2238 - 2243.
Chaves, J., Beirão, I., Balreira, A., Gaspar, P., et al. (2011). Progressive myoclonus epilepsy with nephropathy C1q due to SCARB2/LIMP-2 deficiency: Clinical report of two siblings. Seizure, 20(9), 738 - 740.

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