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Outcomes of liver–kidney transplantation in patients with primary hyperoxaluria: an analysis of the scientific registry of transplant recipients database
BACKGROUND: Primary hyperoxaluria (PH) is an inherited disease lacking of hepatic oxalic acid metabolic enzymes which could lead to irreverisible renal damage. Currently, liver–kidney transplantation is a curative but highly invasive therapy used to treat patients with PH. However, limited studies h...
Autores principales: | Xiang, Jie, Chen, Zheng, Xu, Fangshen, Mei, Shengmin, Li, Zhiwei, Zhou, Jie, Dong, Yinlei, Gu, Yangjun, Huang, Zhichao, Hu, Zhenhua |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333252/ https://www.ncbi.nlm.nih.gov/pubmed/32620094 http://dx.doi.org/10.1186/s12876-020-01349-1 |
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