Diagnostic policies on nephrolithiasis/nephrocalcinosis of possible genetic origin by Italian nephrologists: a survey by the Italian Society of Nephrology with an emphasis on primary hyperoxaluria

BACKGROUND: Primary hyperoxaluria is a genetic disorder of the metabolism of glyoxylate, the precursor of oxalate. It is characterized by high endogenous production and excessive urinary excretion of oxalate, resulting in the development of calcium oxalate nephrolithiasis, nephrocalcinosis, and, in...

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Detalles Bibliográficos
Autores principales: Ferraro, Pietro Manuel, Caletti, Chiara, Capolongo, Giovanna, Lombardi, Marco, Scolari, Francesco, Vezzoli, Giuseppe, Vitale, Corrado, Gambaro, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393840/
https://www.ncbi.nlm.nih.gov/pubmed/37358729
http://dx.doi.org/10.1007/s40620-023-01693-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393840/
https://www.ncbi.nlm.nih.gov/pubmed/37358729
http://dx.doi.org/10.1007/s40620-023-01693-x

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