Primary hyperoxaluria type 1 and end-stage renal disease in a 3-month-old infant
Author:
Affiliation:
1. Fukui Red Cross Hospital
2. Department of Pediatrics, Faculty of Medical Sciences, University of Fukui
3. Department of Health Science, Faculty of Medical Sciences, University of Fukui
Publisher
Japanese Society for Pediatric Nephrology
Subject
Literature and Literary Theory,History,Cultural Studies
Link
https://www.jstage.jst.go.jp/article/jjpn/28/1/28_60/_pdf
Reference15 articles.
1. 1) Hoppe B: Evidence of true genotype-phenotype correlation in primary hyperoxaluria type 1. Kidney Int 2010; 77: 383–385.
2. 2) Cochat P, Koch Nogueira PC, Mahmoud MA, Jamieson NW, Scheinman JL: Primary hyperoxaluria in infant: Medical, ethical, and economic issues. J Pediatr 1999; 35: 746–750.
3. 3) Cochat P, Hulton SA, Acquaviva C, Danpure CJ, Daudon M, De Marchi M, Fargue S, Groothoff J, Harambat J, Hoppe B, Jamieson NV, Kemper MJ, Mandrile G, Marangella M, Picca S, Rumsby G, Salido E, Straub M, van Woerden CS; OxalEurope: Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment. Nephrol Dial Transplant 2012; 27: 1729–1736.
4. 5) Inoue Y, Masuyama H, Ikawa H, Mitubuchi H, Kuhara T: Monitoring method for pre- and post-liver transplantation in patients with primary hyperoxaluria type 1. J Chromatogr B 2003; 792: 89–97.
5. 7) Leumann EP, Niederwiesser A, Fanconi A: New aspects of infantile oxalosis. Pediatr Nephrol 1987; 3: 531–535.
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