A carregar...

Transplantation for Primary Hyperoxaluria Type 1: Designing New Strategies in the Era of Promising Therapeutic Perspectives

Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disease caused by the functional defect of alanine-glyoxylate aminotransferase that results in the overproduction of oxalate. It can be devastating especially for kidneys, leading to end-stage renal disease (ESRD) during the first 2 to 3 d...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Kidney Int Rep
Main Authors: Devresse, Arnaud, Cochat, Pierre, Godefroid, Nathalie, Kanaan, Nada
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7710835/
https://ncbi.nlm.nih.gov/pubmed/33305106
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ekir.2020.09.022
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!