Patients with Fabry Disease after Enzyme Replacement Therapy Dose Reduction and Switch–2-Year Follow-Up

Because of the shortage of agalsidase-β supply between 2009 and 2012, patients with Fabry disease either were treated with reduced doses or were switched to agalsidase-α. In this observational study, we assessed end organ damage and clinical symptoms with special focus on renal outcome after 2 years...

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Vydáno v:J Am Soc Nephrol
Hlavní autoři: Lenders, Malte, Canaan-Kühl, Sima, Krämer, Johannes, Duning, Thomas, Reiermann, Stefanie, Sommer, Claudia, Stypmann, Jörg, Blaschke, Daniela, Üçeyler, Nurcan, Hense, Hans-Werner, Brand, Stefan-Martin, Wanner, Christoph, Weidemann, Frank, Brand, Eva
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society of Nephrology 2016
Témata:
Clinical Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4769208/
https://ncbi.nlm.nih.gov/pubmed/26185201
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2015030337
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