Current approaches to the management of primary hyperoxaluria.
作者信息
Cochat P, Basmaison O
机构信息
Département de Pédiatrie, Hôpital Edouard Herriot and Université Claude Bernard, Lyon, France.
出版信息
Arch Dis Child. 2000 Jun;82(6):470-3. doi: 10.1136/adc.82.6.470.
Abstract
摘要
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本文引用的文献
1
Primary hyperoxaluria in infants: medical, ethical, and economic issues.
J Pediatr. 1999 Dec;135(6):746-50. doi: 10.1016/s0022-3476(99)70095-8.
2
What is new in primary hyperoxaluria?
Nephrol Dial Transplant. 1999 Nov;14(11):2556-8. doi: 10.1093/ndt/14.11.2556.
3
The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II.编码羟基丙酮酸还原酶（GRHPR）的基因在II型原发性高草酸尿症患者中发生突变。
Hum Mol Genet. 1999 Oct;8(11):2063-9. doi: 10.1093/hmg/8.11.2063.
4
Primary hyperoxaluria type 1.1型原发性高草酸尿症
Kidney Int. 1999 Jun;55(6):2533-47. doi: 10.1046/j.1523-1755.1999.00477.x.
5
Transplantation strategies in type 1 primary hyperoxaluria: the issue of pyridoxine responsiveness.1型原发性高草酸尿症的移植策略：维生素B6反应性问题。
Nephrol Dial Transplant. 1999 Feb;14(2):301-3. doi: 10.1093/ndt/14.2.301.
6
Clinical expression and long-term outcomes of primary hyperoxaluria types 1 and 2.1型和2型原发性高草酸尿症的临床表现及长期预后
J Nephrol. 1998 Mar-Apr;11 Suppl 1:56-9.
7
8
Crystalluria: a clinically useful investigation in children with primary hyperoxaluria post-transplantation.结晶尿症：对移植后原发性高草酸尿症患儿的一项临床有用的检查。
Kidney Int. 1998 May;53(5):1412-6. doi: 10.1046/j.1523-1755.1998.00876.x.
9
Kinetic analysis and tissue distribution of human D-glycerate dehydrogenase/glyoxylate reductase and its relevance to the diagnosis of primary hyperoxaluria type 2.人D-甘油酸脱氢酶/乙醛酸还原酶的动力学分析及组织分布及其与原发性高草酸尿症2型诊断的相关性
Ann Clin Biochem. 1998 Jan;35 ( Pt 1):104-9. doi: 10.1177/000456329803500114.
10
A unique molecular basis for enzyme mistargeting in primary hyperoxaluria type 1.1型原发性高草酸尿症中酶靶向错误的独特分子基础。
Clin Chim Acta. 1997 Oct 9;266(1):39-50. doi: 10.1016/s0009-8981(97)00165-4.
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