Associated Papers
Global genetic prevalence estimates of primary hyperoxaluria are greater than previously reported.
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Clinical Kidney Journal, 2025
40873808 (PubMed )
Supplement: sfaf194_Supplemental_File.docx
Burden of Mendelian disorders in a large Middle Eastern biobank.
Aamer W et al.
Genome Medicine, 2024
38584274 (PubMed )
Supplement: 13073_2024_1307_MOESM1_ESM.xlsx › Table_S3
Primary hyperoxaluria diagnosed after kidney transplantation failure: lesson from 3 case reports and literature review.
Cai R et al.
Bmc Nephrology, 2019
Structural basis of substrate specificity in human glyoxylate reductase/hydroxypyruvate reductase.
Booth MP et al.
Journal of Molecular Biology, 2006
Primary hiperoxaluria diagnosed after kidney transplantation: report of 2 cases and literature review.
Rios JFN et al.
Jornal Brasileiro De Nefrologia, 0
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