Liver transplantation for the treatment of urea cycle disorders
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005317909946/fullpdf
Reference16 articles.
1. The use of reduced-size liver transplants in children, including split livers and living related liver transplants;Brolsch;Eur J Pediatr Surg,1991
2. Treatment of inherited metabolic disorders by liver transplantation;Burdelski;J Inher Metab Dis,1991
3. Liver transplantation for metabolic disease of the liver;Esquivel;Gastroenterol Clin N Am,1988
4. Orthotopic liver transplantation for ornithine transcarbamylase deficiency with hyperammonemic encephalopathy;Hasegawa;J Pediatr Surg,1995
5. Histological improvement in native liver after auxiliary partial liver transplantation for ornithine transcarbamylase deficiency [Letter];Inui;Lancet,1996
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1. Impact of supplementation with L-citrulline/arginine after liver transplantation in individuals with Urea Cycle Disorders;Molecular Genetics and Metabolism;2024-03
2. Severity-adjusted evaluation of liver transplantation on health outcomes in Urea Cycle Disorders;Genetics in Medicine;2023-12
3. Lipid nanoparticle-targeted mRNA formulation as a treatment for ornithine-transcarbamylase deficiency model mice;Molecular Therapy - Nucleic Acids;2023-09
4. Citrullinemia in a newborn: a case report;Russian Journal of Child Neurology;2022-12-17
5. Liver transplantation in rare late‐onset ornithine transcarbamylase deficiency with central nervous system injury: A case report and review of the literature;Brain and Behavior;2022-09-20
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