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Published in 2018 at "Pediatric Nephrology"
DOI: 10.1007/s00467-018-4081-5
Abstract: BackgroundPrimary hyperoxaluria type 1 (PH1) is an orphan inborn error of oxalate metabolism leading to hyperoxaluria, progressive renal failure, oxalate deposition, and increased cardiovascular complications. As endothelial dysfunction and arterial stiffness are early markers of…
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Keywords:
dysfunction;
ph1;
ph1 cons;
hyperoxaluria type ... See more keywords