An infant with nephrolithiasis and renal failure: Answers.

作者信息

Ueno Kazuyuki, Shimizu Masaki, Kubo Tatsuya, Igarashi Noboru, Hatasaki Kiyoshi

机构信息

Department of Pediatrics, Toyama Prefectural Central Hospital, Toyama, Japan.

Department of Pediatrics, School of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, 13-1 Takaramachi, Kanazawa, 920-8641, Japan.

出版信息

Pediatr Nephrol. 2016 Jul;31(7):1083-4. doi: 10.1007/s00467-015-3100-z. Epub 2015 Apr 11.

DOI:10.1007/s00467-015-3100-z

PMID:25862022

Abstract

摘要

相似文献

An infant with nephrolithiasis and renal failure: Answers.

Pediatr Nephrol. 2016 Jul;31(7):1083-4. doi: 10.1007/s00467-015-3100-z. Epub 2015 Apr 11.

[2,8-dihydroxyadenine nephrolithiasis: from diagnosis to therapy].

Ann Biol Clin (Paris). 2007 Nov-Dec;65(6):585-92.

Adenine phosphoribosyltransferase deficiency and 2, 8-dihydroxyadenine renal stones: A preventable cause of pediatric renal stones and kidney disease.

Saudi J Kidney Dis Transpl. 2019 May-Jun;30(3):723-725. doi: 10.4103/1319-2442.261357.

Adenine phosphoribosyltransferase deficiency with renal deposition of 2,8-dihydroxyadenine leading to nephrolithiasis and chronic renal failure.

Arch Intern Med. 1993 Mar 22;153(6):767-70.

Chronic tubulointerstitial kidney disease in untreated adenine phosphoribosyl transferase (APRT) deficiency: A case report .

Clin Nephrol. 2018 Oct;90(4):296-301. doi: 10.5414/CN109460.

2,8-Dihydroxyadenine renal stones in a 41-year-old man.

Ann Clin Biochem. 2004 Mar;41(Pt 2):160-1. doi: 10.1258/000456304322880087.

Chronic renal failure in a mouse model of human adenine phosphoribosyltransferase deficiency.

Am J Physiol. 1998 Jul;275(1):F154-63. doi: 10.1152/ajprenal.1998.275.1.F154.

Obstructive uropathy and severe acute kidney injury from renal calculi due to adenine phosphoribosyltransferase deficiency.

World J Pediatr. 2016 May;12(2):243-5. doi: 10.1007/s12519-015-0073-8. Epub 2015 Dec 18.

2,8-Dihydroxyadenine Nephropathy Identified as Cause of End-Stage Renal Disease After Renal Transplant.

Exp Clin Transplant. 2017 Oct;15(5):574-577. doi: 10.6002/ect.2015.0096. Epub 2015 Aug 31.

Clinical features and genotype of adenine phosphoribosyltransferase deficiency in iceland.

Am J Kidney Dis. 2001 Sep;38(3):473-80. doi: 10.1053/ajkd.2001.26826.

本文引用的文献

Decreased kidney function and crystal deposition in the tubules after kidney transplant.

Am J Kidney Dis. 2010 Sep;56(3):585-90. doi: 10.1053/j.ajkd.2009.12.028. Epub 2010 Mar 19.

Phenotype and genotype characterization of adenine phosphoribosyltransferase deficiency.

J Am Soc Nephrol. 2010 Apr;21(4):679-88. doi: 10.1681/ASN.2009080808. Epub 2010 Feb 11.

[2,8-dihydroxyadenine nephrolithiasis: from diagnosis to therapy].

Ann Biol Clin (Paris). 2007 Nov-Dec;65(6):585-92.

8-Hydroxyadenine as the intermediate in the oxidation of adenine to 2, 8-dihydroxyadenine by xanthine oxidase.

Arch Biochem Biophys. 1957 Jul;70(1):150-6. doi: 10.1016/0003-9861(57)90088-7.

Clinical features and genotype of adenine phosphoribosyltransferase deficiency in iceland.

Am J Kidney Dis. 2001 Sep;38(3):473-80. doi: 10.1053/ajkd.2001.26826.

Family study of 2,8-dihydroxyadenine stone formation: report of two cases of a compound heterozygote for adenine phosphoribosyltransferase deficiency (APRT*J/APRT*Q0).

Int J Urol. 1997 May;4(3):304-6. doi: 10.1111/j.1442-2042.1997.tb00195.x.

Adenine phosphoribosyltransferase deficiency: a previously undescribed genetic defect in man.

J Clin Invest. 1968 Oct;47(10):2281-9. doi: 10.1172/JCI105913.

Complete deficiency of adenine phosphoribosyltransferase. Report of a family.

N Engl J Med. 1977 Jul 21;297(3):127-32. doi: 10.1056/NEJM197707212970302.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验