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The Primary Hyperoxalurias

The primary hyperoxalurias are rare disorders of glyoxylate metabolism in which specific hepatic enzyme deficiencies result in overproduction of oxalate. Due to resulting severe hyperoxaluria, recurrent urolithiasis or progressive nephrocalcinosis are the principal manifestations. End stage renal fa...

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Bibliografiske detaljer
Udgivet i:Kidney Int
Main Authors: Hoppe, Bernd, Beck, Bodo B., Milliner, Dawn
Format: Artigo
Sprog:Inglês
Udgivet: 2009
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4577278/
https://ncbi.nlm.nih.gov/pubmed/19225556
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ki.2009.32
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