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Each Association appointed at least one author to serve on the writing group. The Chair of
the writing group was appointed by the AASLD. Members of the writing group were not …

Punishment is a popular tool when governing commons in situations where free riders
would otherwise take over. It is well known that sanctioning systems, such as the police and …

Introduction In primary hyperoxaluria type 1 (PH1), oxalate overproduction frequently causes
kidney stones, nephrocalcinosis, and kidney failure. As PH1 is caused by a congenital liver …

Primary hyperoxaluria type 1 (PH1) is a hepatic metabolic defect leading to end‐stage renal
failure. The posttransplant recurrence of kidney disease can suggest a need for combined …

Loss-of-function mutations in three genes, involved in the metabolic pathway of glyoxylate,
result in increased oxalate production and its crystallization in the form of calcium oxalate …

Primary hyperoxalurias (PH) comprise a group of three distinct metabolic diseases caused
by derangement of glyoxylate metabolism in the liver. Recent years have seen advances in …

Background Primary hyperoxaluria (PH) is an inherited disease lacking of hepatic oxalic
acid metabolic enzymes which could lead to irreverisible renal damage. Currently, liver …

Combined liver‐kidney transplantation (CLKT) is well established as a definitive therapy
with the potential to provide complete recovery for certain liver‐kidney diseases, although …

Purpose of review: To provide transplant physicians with a summary of the pathogenesis
and diagnosis of adenine phosphoribosyl transferase (APRT) deficiency and primary …