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...

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Detalles Bibliográficos
Autores principales: Devresse, Arnaud, Cochat, Pierre, Godefroid, Nathalie, Kanaan, Nada
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710835/
https://www.ncbi.nlm.nih.gov/pubmed/33305106
http://dx.doi.org/10.1016/j.ekir.2020.09.022

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710835/
https://www.ncbi.nlm.nih.gov/pubmed/33305106
http://dx.doi.org/10.1016/j.ekir.2020.09.022

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