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Evaluation and Medical Management of Patients with Cystine Nephrolithiasis: A Consensus Statement

Purpose: Cystinuria is a genetic disorder with both autosomal recessive and incompletely dominant inheritance. The disorder disrupts cystine and other dibasic amino acid transport in proximal tubules of the kidney, resulting in recurrent kidney stone formation. Currently, there are no consensus guid...

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Dettagli Bibliografici
Pubblicato in:J Endourol
Autori principali: Eisner, Brian H., Goldfarb, David S., Baum, Michelle A., Langman, Craig B., Curhan, Gary C., Preminger, Glenn M., Lieske, John C., Pareek, Gyan, Thomas, Kay, Zisman, Anna L., Papagiannopoulos, Dimitri, Sur, Roger L.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Mary Ann Liebert, Inc., publishers 2020
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7869875/
https://ncbi.nlm.nih.gov/pubmed/32066273
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/end.2019.0703
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