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The role of preemptive liver transplantation in primary hyperoxaluria type 1

✍ Scribed by Kemper, Markus J.


Publisher
Springer
Year
2005
Tongue
English
Weight
172 KB
Volume
33
Category
Article
ISSN
0300-5623

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Primary hyperoxaluria type 1: update and
✍ Emma L. Williams; Cecile Acquaviva; Antonio Amoroso; Francoise Chevalier; Marion πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 243 KB

Primary hyperoxaluria type 1 (PH1) is an autosomal recessive, inherited disorder of glyoxylate metabolism arising from a deficiency of the alanine:glyoxylate aminotransferase (AGT) enzyme, encoded by the AGXT gene. The disease is manifested by excessive endogenous oxalate production, which leads to