Long-term outcomes after pre-emptive liver transplantation in primary hyperoxaluria type 1.

Background: Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disease caused by the liver defect of oxalate metabolism, which leads to kidney failure and systemic manifestations. Until recently, liver transplantation was the only definitive treatment. The timing of liver transplantation c...

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Publicado en:	Pediatric Nephrology Vol. 38; no. 6; pp. 1811 - 1821
Autores principales:	Shasha-Lavsky, Hadas, Avni, Aviv, Paz, Ziv, Kalfon, Limor, Dror, Amiel A., Yakir, Orly, Zaccai, Tzipora Falik, Weissman, Irith
Formato:	research tables/charts Journal Article
Publicado:	Springer Nature Jun2023
Acceso en línea:	Ver este registro en EBSCOhost