Aggressive immunotherapy combined with bortezomib and rituximab for membranous nephropathy associated with enzyme replacement therapy in Pompe disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00467-022-05672-5.pdf
Reference15 articles.
1. Kishnani PS, Steiner RD, Bali D, Berger K et al (2006) Pompe disease diagnosis and management guideline. Genet Med 8:267–288. https://doi.org/10.1097/01.gim.0000218152.87434.f3
2. Kishnani PS, Corzo D, Nicolino M, Byrne B et al (2007) Recombinant human acid α-glucosidase: major clinical benefits in infantile-onset Pompe disease. Neurology 68:99–109. https://doi.org/10.1212/01.wnl.0000251268.41188.04
3. Chien YH, Lee NC, Thurberg BL, Chiang SC et al (2009) Pompe disease in infants: improving the prognosis by newborn screening and early treatment. Pediatrics 124:e1116–e1125. https://doi.org/10.1542/peds.2008-3667
4. Toscano A, Schoser B (2013) Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review. J Neurol 260:951–959. https://doi.org/10.1007/s00415-012-6636-x
5. Hanna D, Vassili V, Olivia B, Laure-Helene N et al (2014) Allo-immune membranous nephropathy and recombinant aryl sulfatase replacement therapy: a need for tolerance induction therapy. J Am Soc Nephrol 25:675–680. https://doi.org/10.1681/ASN.2013030290
Cited by 2 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. Optimizing treatment outcomes: immune tolerance induction in Pompe disease patients undergoing enzyme replacement therapy;Frontiers in Immunology;2024-04-23
2. Alglucosidase-alfa;Reactions Weekly;2023-03-18
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