Membranous nephropathy without vacuolated podocytes in Fabry disease treated with agalsidase-β and carbamazepine
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference11 articles.
1. Fabry disease: guidelines for the evaluation and management of multi-organ system involvement;Eng;Genet Med,2006
2. Coexistence of Fabry disease and membranous nephropathy;Liu;Iran J Kidney Dis,2016
3. Coexistence of Fabry disease with IgM nephropathy: a case report;Wu;Medicine (Baltimore),2019
4. Foot process effacement with normal urinalysis in classic Fabry disease;Kanai;JIMD Rep,2011
5. Surges in proteinuria are associated with plasma GL-3 elevations in a young patient with classic Fabry disease;Kanai;Eur J Pediatr,2016
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Diagnosing Fabry nephropathy: the challenge of multiple kidney disease;BMC Nephrology;2023-11-21
2. Fabry Disease Nephropathy: Histological Changes With Nonclassical Mutations and Genetic Variants of Unknown Significance;American Journal of Kidney Diseases;2023-11
3. Agalsidase-β/carbamazepine;Reactions Weekly;2022-04
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