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Fabry disease in donor kidneys with 3- and 12-year follow-up after transplantation
Enzyme replacement therapy (ERT) has been introduced for Fabry disease and has been reported to clear some renal cell types of accumulated glycolipids and to reduce the accumulation in other cell types. We describe two patients without Fabry disease who were transplanted with kidney allografts from...
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| Vydáno v: | NDT Plus |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5477959/ https://ncbi.nlm.nih.gov/pubmed/28657066 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ndtplus/sfq036 |
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