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Recovery From Dialysis in Patients With Primary Hyperoxaluria Type 1 Treated With Pyridoxine: A Report of 3 Cases
Primary hyperoxaluria type 1 (PH1) is a genetic disorder characterized by overproduction of oxalate and eventual kidney failure. Kidney failure is usually irreversible in PH1. However, in PH1 patients homozygous for the G170R mutation, pyridoxine is an enzyme co-factor and decreases urine oxalate ex...
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| Publicat a: | Am J Kidney Dis |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7930154/ https://ncbi.nlm.nih.gov/pubmed/32891627 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1053/j.ajkd.2020.07.017 |
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