Abstract
The primary hyperoxalurias (PHs) are a group of rare genetic disorders affecting glyoxylate metabolism, leading to excessive oxalate production, a metabolic end-product. This overproduction can result in nephrocalcinosis, recurrent kidney stone formation and kidney failure. The clinical course of PH is highly variable, ranging from patients developing kidney failure in infancy to
| Original language | English |
|---|---|
| Qualification | Doctor of Philosophy |
| Awarding Institution |
|
| Supervisors/Advisors |
|
| Award date | 2 May 2025 |
| Print ISBNs | 9789465221656 |
| Publication status | Published - 2025 |
Fingerprint
Dive into the research topics of 'Stepping stones to targeted treatment of primary hyperoxaluria'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver