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2013
A. M. Martins, Kyosen, S. O., Garrote, J., Marques, F. M. V., Guilhem, J. G., Macedo, E., J. Neto, S., and Ura, S., Demographic characterization of Brazilian patients enrolled in the Fabry Registry, vol. 12, pp. 136-142, 2013.
Anonymous (2011). Available at [www.brasil.gov.br/sobre/geografia/populacao/etnias]. Accessed October 19, 2011.   Branton MH, Schiffmann R, Sabnis SG, Murray GJ, et al. (2002). Natural history of Fabry renal disease: influence of alpha-galactosidase A activity and genetic mutations on clinical course. Medicine 81: 122-138. http://dx.doi.org/10.1097/00005792-200203000-00003 PMid:11889412   Desnick RJ, Ioannou YA and Eng CM (2001). Alpha-Galactosidase A Deficiency: Fabry Disease. In: The Metabolic Bases of Inherited Disease (Scriver C, Beaudet A, Sly W and Valle D, eds.). 8th edn. McGraw-Hill, New York, 3733-3774.   Eng CM, Fletcher J, Wilcox WR, Waldek S, et al. (2007). Fabry disease: baseline medical characteristics of a cohort of 1765 males and females in the Fabry Registry. J. Inherit. Metab. Dis. 30: 184-192. http://dx.doi.org/10.1007/s10545-007-0521-2 PMid:17347915   Hopkin RJ, Bissler J, Banikazemi M, Clarke L, et al. (2008). Characterization of Fabry disease in 352 pediatric patients in the Fabry Registry. Pediatr. Res. 64: 550-555. http://dx.doi.org/10.1203/PDR.0b013e318183f132 PMid:18596579   Mehta A, Ricci R, Widmer U, Dehout F, et al. (2004). Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey. Eur. J. Clin. Invest. 34: 236-242. http://dx.doi.org/10.1111/j.1365-2362.2004.01309.x PMid:15025684   Schiffmann R, Warnock DG, Banikazemi M, Bultas J, et al. (2009). Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy. Nephrol. Dial. Transplant. 24: 2102-2111. http://dx.doi.org/10.1093/ndt/gfp031 PMid:19218538 PMCid:2698092   Sims K, Politei J, Banikazemi M and Lee P (2009). Stroke in Fabry disease frequently occurs before diagnosis and in the absence of other clinical events: natural history data from the Fabry Registry. Stroke 40: 788-794. http://dx.doi.org/10.1161/STROKEAHA.108.526293 PMid:19150871   Wilcox WR, Oliveira JP, Hopkin RJ, Ortiz A, et al. (2008). Females with Fabry disease frequently have major organ involvement: lessons from the Fabry Registry. Mol. Genet. Metab. 93: 112-128. http://dx.doi.org/10.1016/j.ymgme.2007.09.013 PMid:18037317