Pediatrics: Timely diagnosis of primary hyperoxaluria type 1.

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作者信息

Chand Alejandro Quiroga, Kaskel Frederick J

出版信息

Nat Rev Nephrol. 2009 Dec;5(12):670-1. doi: 10.1038/nrneph.2009.186.

DOI:10.1038/nrneph.2009.186

PMID:19935811

Abstract

摘要

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Alanine-glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer.

Proc Natl Acad Sci U S A. 2006 Nov 28;103(48):18249-54. doi: 10.1073/pnas.0607218103. Epub 2006 Nov 16.

Primary hyperoxaluria type 1: still challenging!

Pediatr Nephrol. 2006 Aug;21(8):1075-81. doi: 10.1007/s00467-006-0124-4. Epub 2006 Jun 30.

Implications of genotype and enzyme phenotype in pyridoxine response of patients with type I primary hyperoxaluria.

Am J Nephrol. 2005 Mar-Apr;25(2):183-8. doi: 10.1159/000085411. Epub 2005 Apr 21.

A United States survey on diagnosis, treatment, and outcome of primary hyperoxaluria.

Pediatr Nephrol. 2003 Oct;18(10):986-91. doi: 10.1007/s00467-003-1234-x. Epub 2003 Aug 15.

Results of long-term treatment with orthophosphate and pyridoxine in patients with primary hyperoxaluria.

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相似文献

Pediatrics: Timely diagnosis of primary hyperoxaluria type 1.

Nat Rev Nephrol. 2009 Dec;5(12):670-1. doi: 10.1038/nrneph.2009.186.

Oxalosis with nephrocalcinosis.

Nephrol Dial Transplant. 2000 Jan;15(1):124-5. doi: 10.1093/ndt/15.1.124.

Off-center fold: necrotizing livedo reticularis. Diagnosis: primary hyperoxaluria type I.

Arch Dermatol. 2001 Jul;137(7):957-62.

Primary Hyperoxaluria.

N Engl J Med. 2022 Mar 10;386(10):976. doi: 10.1056/NEJMicm2113369. Epub 2022 Mar 5.

A 2-month-old female infant with failure to thrive.

Pediatr Ann. 2013 May;42(5):191-3. doi: 10.3928/00904481-20130426-06.

Primary hyperoxaluria type 2.

Eur J Pediatr. 1997 Jul;156(7):509-12. doi: 10.1007/s004310050649.

Atypical features of primary hyperoxaluria in end-stage renal disease.

Am J Nephrol. 1991;11(4):301-4. doi: 10.1159/000168326.

Primary hyperoxaluria.

N Engl J Med. 2013 Aug 15;369(7):649-58. doi: 10.1056/NEJMra1301564.

Bone disease of primary hyperoxaluria in infancy.

Pediatr Radiol. 1989;20(1-2):131-3. doi: 10.1007/BF02010661.

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Kidney Int. 1999 Jun;55(6):2533-47. doi: 10.1046/j.1523-1755.1999.00477.x.

引用本文的文献

Oxalate Nephropathy and the Mechanism of Oxalate-Induced Kidney Injury.

Kidney Dis (Basel). 2023 Jul 27;9(6):459-468. doi: 10.1159/000533295. eCollection 2023 Dec.

[Oliguria and acute renal dysfunction in a six-month-old infant].

Zhongguo Dang Dai Er Ke Za Zhi. 2017 Feb;19(2):203-207. doi: 10.7499/j.issn.1008-8830.2017.02.015.

本文引用的文献

Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1.

Kidney Int. 2009 Oct;76(7):767-73. doi: 10.1038/ki.2009.237. Epub 2009 Jul 1.

Alanine-glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer.

Proc Natl Acad Sci U S A. 2006 Nov 28;103(48):18249-54. doi: 10.1073/pnas.0607218103. Epub 2006 Nov 16.

Primary hyperoxaluria type 1: still challenging!

Pediatr Nephrol. 2006 Aug;21(8):1075-81. doi: 10.1007/s00467-006-0124-4. Epub 2006 Jun 30.

Implications of genotype and enzyme phenotype in pyridoxine response of patients with type I primary hyperoxaluria.

Am J Nephrol. 2005 Mar-Apr;25(2):183-8. doi: 10.1159/000085411. Epub 2005 Apr 21.

A United States survey on diagnosis, treatment, and outcome of primary hyperoxaluria.

Pediatr Nephrol. 2003 Oct;18(10):986-91. doi: 10.1007/s00467-003-1234-x. Epub 2003 Aug 15.

Results of long-term treatment with orthophosphate and pyridoxine in patients with primary hyperoxaluria.

N Engl J Med. 1994 Dec 8;331(23):1553-8. doi: 10.1056/NEJM199412083312304.