Primary hyperoxaluria Type 1
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference19 articles.
1. Epidemiology of primary hyperoxaluria type 1;Cochat;Nephrol Dial Transplant,1995
2. Primary hyperoxaluria type 1 in the Netherlands: prevalence and outcome;van Woerden;Nephrol Dial Transplant,2003
3. Evaluation of mutation screening as a first line test for the diagnosis of the primary hyperoxalurias;Rumsby;Kidney Int,2004
4. Phenotype-genotype correlations and estimated carrier frequencies of primary hyperoxaluria;Hopp;J Am Soc Nephrol,2015
5. Crystallization and preliminary crystallographic analysis of human alanine:glyoxylate aminotransferase and its polymorphic variants;Zhang;Acta Crystallogr D Biol Crystallogr,2001
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Molecular Analysis of the AGXT Gene Detected a Missense and Pathogenic Variant Associated with Primary Hyperoxaluria Type 1; a Case Study;2023-11-29
2. Identification of mutations in 15 nephrolithiasis-related genes leading to a molecular diagnosis in 85 Chinese pediatric patients;Pediatric Nephrology;2023-06-12
3. Clinical experience of using denosumab in the treatment of hypercalcemia and oxalate osteopathy for a young patient with primary hyperoxaluria type 1.;Osteoporosis and Bone Diseases;2021-02-27
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