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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Dades bibliogràfiques
Publicat a:J Endourol
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: Mary Ann Liebert, Inc., publishers 2020
Matèries:
Review Articles
Accés en línia: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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