Primary Hyperoxaluria: Clinical Course, Diagnosis, and Treatment After Kidney Failure
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference17 articles.
1. Primary hyperoxaluria;Danpure,2001
2. Is there a genotype-phenotype correlation in primary hyperoxaluria type 1?;Beck;Kidney Int,2006
3. Primary hyperoxaluria type 1: Still challenging!;Cochat;Pediatr Nephrol,2006
4. The primary hyperoxalurias;Leumann;J Am Soc Nephrol,2001
5. Primary hyperoxaluria type 1;Cochat;Kidney Int,1999
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1. Primary hyperoxaluria type 1—a rare hereditary metabolic disorder as cause of livedo racemosa;Die Dermatologie;2024-01-02
2. Dual Glycolate Oxidase/Lactate Dehydrogenase A Inhibitors for Primary Hyperoxaluria;ACS Medicinal Chemistry Letters;2021-05-20
3. Plasma oxalate levels in primary hyperoxaluria type I show significant intra-individual variation and do not correlate with kidney function;Pediatric Nephrology;2020-04-09
4. HPO2Vec+: Leveraging heterogeneous knowledge resources to enrich node embeddings for the Human Phenotype Ontology;Journal of Biomedical Informatics;2019-08
5. Association of Urinary Oxalate Excretion With the Risk of Chronic Kidney Disease Progression;JAMA Internal Medicine;2019-04-01
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