The prevalence of Fabry disease in a Turkish population with chronic kidney patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Urology,Nephrology
Link
https://link.springer.com/content/pdf/10.1007/s11255-023-03488-2.pdf
Reference27 articles.
1. Ito S, Ogura M, Kamei K, Matsuoka K, Warnock DG (2016) Significant improvement in Fabry disease podocytopathy after 3 years of treatment with agalsidase beta. Pediatr Nephrol 31:1369–1373. https://doi.org/10.1007/s00467-016-3387-4
2. Kanai T, Yamagata T, Ito T, Odaka J, Saito T, Aoyagi J, Kobayashi M, Ohashi T, Ueda Y, Momoi MY (2011) Foot process effacement with normal urinalysis in classic Fabry disease. JIMD Rep 1:39–42. https://doi.org/10.1007/8904_2011_14
3. Germain DP (2010) Fabry disease. Orphanet J Rare Dis 5:30. https://doi.org/10.1186/1750-1172-5-30
4. Wang RY, Lelis A, Mirocha J, Wilcox WR (2007) Heterozygous Fabry women are not just carriers, but have a significant burden of disease and impaired quality of life. Genet Med 9:34–45. https://doi.org/10.1097/gim.0b013e31802d8321
5. Wilcox WR, Oliveira JP, Hopkin RJ, Ortiz A, Banikazemi M, Feldt-Rasmussen U, Sims K, Waldek S, Pastores GM, Lee P, Eng CM, Marodi L, Stanford KE, Breunig F, Wanner C, Warnock DG, Lemay RM, Germain DP, Fabry R (2008) Females with Fabry disease frequently have major organ involvement: lessons from the Fabry Registry. Mol Genet Metab 93:112–128. https://doi.org/10.1016/j.ymgme.2007.09.013
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