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Magnesium lactate in the treatment of Gitelman syndrome: patient-reported outcomes
Background: Gitelman syndrome (GS) is a rare recessively inherited renal tubulopathy associated with renal potassium (K) and magnesium (Mg) loss. It requires lifelong K and Mg supplementation at high doses that are at best unpalatable and at worst, intolerable. In particular, gastrointestinal side e...
Shranjeno v:
| izdano v: | Nephrol Dial Transplant |
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| Main Authors: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Oxford University Press
2017
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5837242/ https://ncbi.nlm.nih.gov/pubmed/26940126 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ndt/gfw019 |
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