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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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Dades bibliogràfiques
Publicat a:Am J Kidney Dis
Autors principals: Lorenz, Elizabeth C., Lieske, John C., Seide, Barbara M., Olson, Julie B., Mehta, Ramila, Milliner, Dawn S.
Format: Artigo
Idioma:Inglês
Publicat: 2020
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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