Hyperoxaluria
Author:
Publisher
Springer Berlin Heidelberg
Link
https://link.springer.com/content/pdf/10.1007/978-3-642-27843-3_39-2
Reference78 articles.
1. Cochat P, Rumsby G. Primary hyperoxaluria. N Engl J Med. 2013;369:649–58.
2. Reusz GS, Dobos M, Byrd D, Sallay P, Miltényi M, Tulassay T. Urinary calcium and oxalate excretion in children. Pediatr Nephrol. 1995;9:39–44.
3. Zhao F, Bergstralh EJ, Mahta RA, Vaughan LE, Olson JB, Seide BM, et al. Predictors of incident ESKD among patients with primary hyperoxaluria presenting prior to kidney failure. Clin J Am Soc Nephrol. 2016;11:119–26.
4. Hopp K, Cogal AG, Bergstralh EJ, Seide BM, Olson JB, Meek AM, et al. Phenotype-genotype correlations and estimated carrier frequencies of primary hyperoxaluria. J Am Soc Nephrol. 2015;26:2559–70.
5. Harambat J, Fargue S, Acquaviva C, Gagnadoux MF, Janssen F, Liutkus A, et al. Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg mutation is associated with better outcome. Kidney Int. 2010;77:443–9.
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