Long-term outcomes after pre-emptive liver transplantation in primary hyperoxaluria type 1
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00467-022-05803-y.pdf
Reference38 articles.
1. Cochat P, Rumsby G (2013) Primary Hyperoxaluria. N Engl J Med 369:649–658. https://doi.org/10.1056/NEJMra1301564
2. Danpure CJ (1991) Molecular and clinical heterogeneity in primary hyperoxaluria type. Am J Kidney Dis 17:366–369. https://doi.org/10.1016/s0272-6386(12)80624-x
3. Ben-Shalom E, Cytter-Kuint R, Choni R, Becker-Cohen R, Tzvi-Behr S, Goichberg J, Peles V, Frishberg Y (2021) Long-term complications of systemic oxalosis in children-a retrospective single-center cohort study. Pediatr Nephrol 36:3123–3132. https://doi.org/10.1007/s00467-021-05002-1
4. Lieske JC, Monico CG, Holmes WS, Bergstralh EJ, Slezak JM, Rohlinger AL, Olson JB, Milliner DS (2005) International registry for primary hyperoxaluria. Am J Nephrol 25:290–296. https://doi.org/10.1159/000086360
5. Hoppe B, Langman CB (2003) A United States survey on diagnosis, treatment, and outcome of primary hyperoxaluria. Pediatr Nephrol 18:986–991. https://doi.org/10.1007/s00467-003-1234-x
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