Long-term therapy with agalsidase alfa for Fabry disease: safety and effects on renal function in a home infusion setting
Abstract. Background. Fabry disease is an X-linked disorder of glycosphingolipid catabolism that is the result of an intracellular deficiency in the lysosomal
Gespeichert in:
| Hauptverfasser: | , , , , |
|---|---|
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2006
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| In: |
Nephrology, dialysis, transplantation
Year: 2005, Jahrgang: 21, Heft: 2, Pages: 345-354 |
| ISSN: | 1460-2385 |
| DOI: | 10.1093/ndt/gfi152 |
| Online-Zugang: | Verlag, Volltext: https://doi.org/10.1093/ndt/gfi152 Verlag, Volltext: https://academic.oup.com/ndt/article/21/2/345/1850640 
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| Verfasserangaben: | Raphael Schiffmann, Markus Ries, Margaret Timmons, John T. Flaherty and Roscoe O. Brady |
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