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Transplantation outcomes in patients with primary hyperoxaluria: a systematic review

BACKGROUND: Primary hyperoxaluria type 1 (PH1) is characterized by hepatic overproduction of oxalate and often results in kidney failure. Liver-kidney transplantation is recommended, either combined (CLKT) or sequentially performed (SLKT). The merits of SLKT and the place of an isolated kidney trans...

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Dades bibliogràfiques
Publicat a:Pediatr Nephrol
Autors principals: Metry, Elisabeth L., van Dijk, Liza M. M., Peters-Sengers, Hessel, Oosterveld, Michiel J.S., Groothoff, Jaap W., Ploeg, Rutger J., Stel, Vianda S., Garrelfs, Sander F.
Format: Artigo
Idioma:Inglês
Publicat: Springer Berlin Heidelberg 2021
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8260423/
https://ncbi.nlm.nih.gov/pubmed/33830344
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-021-05043-6
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