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Glyoxylate reductase activity in blood mononuclear cells and the diagnosis of primary hyperoxaluria type 2
BACKGROUND: Primary hyperoxaluria type 2 (PH2) is a rare monogenic disorder characterized by an elevated urinary excretion of oxalate. Increased oxalate excretion in PH2 patients can cause nephrolithiasis and nephrocalcinosis, and can, in some cases, result in renal failure and systemic oxalate depo...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1579247/ https://ncbi.nlm.nih.gov/pubmed/16597637 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ndt/gfl142 |
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