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本文引用的文献

1
Non-steroidal anti-inflammatories and the development of analgesic nephropathy: a systematic review.非甾体抗炎药与镇痛性肾病的发展：一项系统综述
Ren Fail. 2016 Oct;38(9):1328-1334. doi: 10.1080/0886022X.2016.1216708. Epub 2016 Aug 5.
2
The modern spectrum of renal biopsy findings in patients with diabetes.糖尿病患者肾活检的现代表现谱。
Clin J Am Soc Nephrol. 2013 Oct;8(10):1718-24. doi: 10.2215/CJN.02510213. Epub 2013 Jul 25.
3
Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study.线粒体DNA 3243位点突变患者的视网膜和肾脏并发症（母系遗传糖尿病和耳聋）。一项病例对照研究。
Diabetologia. 2008 Sep;51(9):1664-70. doi: 10.1007/s00125-008-1073-1. Epub 2008 Jun 26.
4
Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.与3243A>G线粒体点突变相关的母系遗传糖尿病和耳聋（MIDD）的临床特征、诊断及管理
Diabet Med. 2008 Apr;25(4):383-99. doi: 10.1111/j.1464-5491.2008.02359.x. Epub 2008 Feb 18.
5
Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD).线粒体DNA 3243 bp突变患者（母系遗传糖尿病伴耳聋或MIDD）糖尿病表型的异质性。
Diabetes Metab. 2004 Apr;30(2):181-6. doi: 10.1016/s1262-3636(07)70105-2.
6
Two-year prospective evaluation of the factors affecting honeymoon frequency and duration in children with insulin dependent diabetes mellitus: the key-role of age at diagnosis.胰岛素依赖型糖尿病患儿蜜月期频率和持续时间影响因素的两年前瞻性评估：诊断时年龄的关键作用
Diabetes Nutr Metab. 2002 Aug;15(4):246-51.
7
Mitochondrial gene mutations in the tRNA(Leu(UUR)) region and diabetes: prevalence and clinical phenotypes in Japan.线粒体tRNA（Leu（UUR））区域基因突变与糖尿病：日本的患病率及临床表型
Clin Chem. 2001 Sep;47(9):1641-8.
8
Heterogeneous presentation in A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene.线粒体tRNA（Leu（UUR））基因A3243G突变的异质性表现
Arch Dis Child. 2000 May;82(5):407-11. doi: 10.1136/adc.82.5.407.
9
The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.辅酶Q10治疗对母系遗传糖尿病伴耳聋及线粒体DNA 3243（A到G）突变的影响。
Diabetologia. 1998 May;41(5):584-8. doi: 10.1007/s001250050950.
10
Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.与进行性肾病相关的线粒体tRNA（Leu（UUR））基因突变。
J Am Soc Nephrol. 1997 Jul;8(7):1118-24. doi: 10.1681/ASN.V871118.

Diabetes and nephrotic syndrome: Answers.

作者信息

Gilbert Rodney D, Hind Edward, Vadgama Bhumita

机构信息

Southampton Children's Hospital and University of Southampton School of Medicine, Tremona Road, Southampton, SO16 6YD, UK.

Hampshire Hospitals NHS Foundation Trust, Basingstoke, Hampshire, UK.

出版信息

Pediatr Nephrol. 2017 Oct;32(10):1887-1889. doi: 10.1007/s00467-016-3560-9. Epub 2016 Dec 23.

DOI:10.1007/s00467-016-3560-9
PMID:28012006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5579146/
Abstract
摘要