Articles with "juvenile ph1" as a keyword



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Long-term outcome after combined or sequential liver and kidney transplantation in children with infantile and juvenile primary hyperoxaluria type 1

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Published in 2023 at "Frontiers in Pediatrics"

DOI: 10.3389/fped.2023.1157215

Abstract: Introduction Combined or sequential liver and kidney transplantation (CLKT/SLKT) restores kidney function and corrects the underlying metabolic defect in children with end-stage kidney disease in primary hyperoxaluria type 1 (PH1). However, data on long-term outcome,… read more here.

Keywords: long term; kidney; transplantation; ph1 ... See more keywords