Outcomes of liver–kidney transplantation in patients with primary hyperoxaluria: an analysis of the scientific registry of transplant recipients database

Abstract 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 s...

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Autors principals:	Jie Xiang, Zheng Chen, Fangshen Xu, Shengmin Mei, Zhiwei Li, Jie Zhou, Yinlei Dong, Yangjun Gu, Zhichao Huang, Zhenhua Hu
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2020-07-01
Col·lecció:	BMC Gastroenterology
Matèries:	Primary hyperoxaluria Inherited disease Liver–kidney transplantation Combined liver and kidney transplantation Sequential liver and kidney transplantation
Accés en línia:	http://link.springer.com/article/10.1186/s12876-020-01349-1
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