Publications
Found 1 results
Filters: Author is S.O. Kyosen [Clear All Filters]
“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