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2,8-Dihydroxyadeninuria-induced progressive renal failure.

作者信息

Mac-Way Fabrice, Desmeules Simon, Latulippe Eva, de Cotret Paul René, Agharazii Mohsen

机构信息

Divisions of Nephrology.

Pathology, Centre Hospitalier Universitaire de Québec, L'Hôtel-Dieu de Québec Hospital and Faculty of Medicine, Laval University, Quebec, Canada.

出版信息

NDT Plus. 2008 Dec;1(6):437-439. doi: 10.1093/ndtplus/sfn110. Epub 2008 Aug 8.

DOI:10.1093/ndtplus/sfn110
PMID:28656998
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5477863/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d29/5477863/26d0fbedaad5/sfn110fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d29/5477863/d79408e36e88/sfn110fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d29/5477863/26d0fbedaad5/sfn110fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d29/5477863/d79408e36e88/sfn110fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d29/5477863/26d0fbedaad5/sfn110fig2.jpg

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本文引用的文献

1
Diagnosis of adenine phosphoribosyltransferase deficiency as the underlying cause of renal failure in a renal transplant recipient.诊断腺嘌呤磷酸核糖转移酶缺乏为一名肾移植受者肾衰竭的潜在病因。
Nephrol Dial Transplant. 2004 Mar;19(3):736-8. doi: 10.1093/ndt/gfg562.
2
Clinical features and genotype of adenine phosphoribosyltransferase deficiency in iceland.冰岛腺嘌呤磷酸核糖转移酶缺乏症的临床特征与基因型
Am J Kidney Dis. 2001 Sep;38(3):473-80. doi: 10.1053/ajkd.2001.26826.
3
Chronic renal failure in a mouse model of human adenine phosphoribosyltransferase deficiency.
人类腺嘌呤磷酸核糖转移酶缺乏小鼠模型中的慢性肾衰竭
Am J Physiol. 1998 Jul;275(1):F154-63. doi: 10.1152/ajprenal.1998.275.1.F154.
4
Recurrence of 2,8-dihydroxyadenine tubulointerstitial lesions in a kidney transplant recipient with a primary presentation of chronic renal failure.一名以慢性肾衰竭为主要表现的肾移植受者出现2,8 - 二羟基腺嘌呤肾小管间质病变复发。
Nephrol Dial Transplant. 1998 Apr;13(4):998-1000. doi: 10.1093/ndt/13.4.998.
5
Acute renal failure in a middle-aged woman with 2,8-dihydroxyadeninuria.一名患有2,8-二羟基腺嘌呤尿症的中年女性的急性肾衰竭。
Nephrol Dial Transplant. 1997 Sep;12(9):1985-7. doi: 10.1093/ndt/12.9.1985.
6
Adenine phosphoribosyltransferase deficiency identified by urinary sediment analysis: cellular and molecular confirmation.通过尿沉渣分析鉴定腺嘌呤磷酸核糖转移酶缺乏症:细胞和分子层面的确认
Clin Genet. 1995 Nov;48(5):246-50. doi: 10.1111/j.1399-0004.1995.tb04098.x.
7
Renal failure due to 2,8-dihydroxyadenine urolithiasis.2,8 - 二羟基腺嘌呤尿路结石所致肾衰竭
Eur J Pediatr. 1982 Jul;138(4):346-9. doi: 10.1007/BF00442515.
8
2,8-Dihydroxyadenine urolithiasis, an underdiagnosed disease.
Lancet. 1992 Apr 25;339(8800):1050-1.
9
The identification of 2,8-dihydroxyadenine, a new component of urinary stones.尿结石新成分2,8 - 二羟基腺嘌呤的鉴定
Biochem J. 1976 Aug 1;157(2):485-7. doi: 10.1042/bj1570485.