The real world experience of pediatric primary hyperoxaluria patients in the PEDSnet clinical research network
Author:
Funder
Dicerna Pharmaceuticals
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00431-023-05077-y.pdf
Reference50 articles.
1. Hopp K, Cogal AG, Bergstralh EJ, Seide BM, Olson JB, Meek AM et al (2015) Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria. J Am Soc Nephrol 26:2559–2570. https://doi.org/10.1681/ASN.2014070698
2. Hoppe B, Beck BB, Milliner DS (2009) The primary hyperoxalurias. Kidney Int 75:1264–1271. https://doi.org/10.1038/ki.2009.32
3. Ventzke A, Feldkotter M, Wei A, Becker J, Beck BB, Hoppe B (2017) Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow-up of primary hyperoxaluria type III. Pediatr Nephrol 32:2263–71. https://doi.org/10.1007/s00467-017-3731-3
4. Lieske JC, Monico CG, Holmes WS, Bergstralh EJ, Slezak JM, Rohlinger AL et al (2005) International registry for primary hyperoxaluria. Am J Nephrol 25:290–6. https://doi.org/10.1159/000086360
5. van der Hoeven SM, van Woerden CS, Groothoff JW (2012) Primary hyperoxaluria type 1, a too often missed diagnosis and potentially treatable cause of end-stage renal disease in adults: results of the Dutch cohort. Nephrol Dial Transplant 27:3855–3862. https://doi.org/10.1093/ndt/gfs320
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