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- W2015051686 abstract "Patientswith inborn errors of metabolism undergo liver transplantation, but the effectof transplanting the liver of healthy carriers of these conditions has notbeen fully clarified. A 6-year-old girl with classical citrullinemia, whorepeatedly suffered from hyperammonemia, underwent living-related livertransplantation by using a segment of the liver of her mother, who was aheterozygote carrier for classical citrullinemia. Hyperammonemia alleviated inthe patient after the transplantation, thereby dramatically improving herquality of life. Although the levels of plasma and urinary citrulline remainedhigh postoperatively, there was no marked difference in the level of plasmacitrulline up to 1 month after surgery when compared with that of previouslyreported orthotopic liver transplantation cases with classicalcitrullinemia." @default.
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- W2015051686 date "2001-05-01" @default.
- W2015051686 modified "2023-10-16" @default.
- W2015051686 title "A PEDIATRIC PATIENT WITH CLASSICAL CITRULLINEMIA WHO UNDERWENT LIVING-RELATED PARTIAL LIVER TRANSPLANTATION" @default.
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- W2015051686 doi "https://doi.org/10.1097/00007890-200105270-00026" @default.
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