• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Unilateral renal agenesis and the congenital solitary functioning kidney: developmental, genetic and clinical perspectives.

作者信息

Woolf Adrian S, Hillman Katherine A

机构信息

Nephro-Urology Unit, UCL Institute of Child Health, and Centre for Nephrology, Royal Free and University College Medical School, London, UK.

出版信息

BJU Int. 2007 Jan;99(1):17-21. doi: 10.1111/j.1464-410X.2006.06504.x. Epub 2006 Sep 6.

DOI:10.1111/j.1464-410X.2006.06504.x
PMID:16956352
Abstract
摘要

相似文献

1
Unilateral renal agenesis and the congenital solitary functioning kidney: developmental, genetic and clinical perspectives.单侧肾缺如与先天性孤立功能肾:发育、遗传及临床视角
BJU Int. 2007 Jan;99(1):17-21. doi: 10.1111/j.1464-410X.2006.06504.x. Epub 2006 Sep 6.
2
Hypertension and microalbuminuria in children with congenital solitary kidneys.先天性孤立肾患儿的高血压与微量白蛋白尿
J Paediatr Child Health. 2008 Jun;44(6):363-8. doi: 10.1111/j.1440-1754.2008.01315.x.
3
Genetic approaches to human renal agenesis/hypoplasia and dysplasia.人类肾发育不全/发育不良的遗传学研究方法。
Pediatr Nephrol. 2007 Oct;22(10):1675-84. doi: 10.1007/s00467-007-0479-1. Epub 2007 Apr 17.
4
Magnetic resonance imaging diagnosis of severe fetal renal anomalies.胎儿严重肾异常的磁共振成像诊断
Am J Obstet Gynecol. 2008 Mar;198(3):328.e1-5. doi: 10.1016/j.ajog.2007.09.032. Epub 2007 Nov 26.
5
[Solitary kidney].
Pediatr Med Chir. 2002 Jul-Aug;24(4):274-8.
6
Clinical outcome of orthotopic neobladder replacement in patients with a solitary functioning kidney.孤立功能性肾患者原位新膀胱置换的临床结局
Int J Urol. 2007 May;14(5):398-401. doi: 10.1111/j.1442-2042.2006.01730.x.
7
Loss of ICAT gene function leads to arrest of ureteric bud branching and renal agenesis.ICAT基因功能丧失导致输尿管芽分支停滞和肾发育不全。
Biochem Biophys Res Commun. 2007 Nov 3;362(4):988-94. doi: 10.1016/j.bbrc.2007.08.085. Epub 2007 Aug 27.
8
Spectrum of congenital renal anomalies presenting in adulthood.成年期出现的先天性肾脏异常谱。
Clin Imaging. 2008 May-Jun;32(3):183-91. doi: 10.1016/j.clinimag.2007.12.001.
9
Dysplastic kidney and not renal agenesis is the commonly associated anomaly in infants with seminal vesicle cyst.发育异常的肾脏而非肾缺如,是患有精囊囊肿的婴儿中常见的相关异常情况。
BJU Int. 2009 Mar;103(6):816-9. doi: 10.1111/j.1464-410X.2008.08072.x. Epub 2008 Nov 25.
10
[Renal agenesis. Apropos of 9 cases].
Tunis Med. 1995 Dec;73(12):547-50.

引用本文的文献

1
Unilateral Renal Agenesis: Prenatal Diagnosis and Postnatal Issues.单侧肾缺如:产前诊断与产后问题
Diagnostics (Basel). 2025 Jun 20;15(13):1572. doi: 10.3390/diagnostics15131572.
2
A surveillance-based epidemiological study of renal agenesis in 25 million births in china, 2007-2020.2007年至2020年中国2500万例出生人口中肾缺如的基于监测的流行病学研究。
BMC Pregnancy Childbirth. 2025 Jul 2;25(1):689. doi: 10.1186/s12884-025-07807-6.
3
Retroperitoneal cysts with congential, ipsilateral renal agenesis of left kidney: a case report.
伴有先天性左肾同侧肾缺如的腹膜后囊肿:病例报告
Ann Med Surg (Lond). 2025 May 12;87(6):3969-3972. doi: 10.1097/MS9.0000000000003347. eCollection 2025 Jun.
4
A renal aplasia case mimicking radiologically as unilateral renal agenesis in a child with spina bifida, atresia ani and unilateral undescended testis: a case report.一名患有脊柱裂、肛门闭锁和单侧隐睾的儿童,其肾脏发育不全病例在影像学上表现为单侧肾缺如:病例报告。
J Med Case Rep. 2024 Jan 26;18(1):31. doi: 10.1186/s13256-023-04330-0.
5
Perioperative, functional, and oncological outcomes after cryoablation or partial nephrectomy for small renal masses in solitary kidneys: a systematic review and meta-analysis.单肾小体积肿瘤行冷冻消融或部分肾切除术的围手术期、功能和肿瘤学结局:系统评价和荟萃分析。
BMC Urol. 2024 Jan 24;24(1):19. doi: 10.1186/s12894-024-01406-x.
6
Environmental and parental risk factors for congenital solitary functioning kidney - a case-control study.先天性孤立功能肾的环境和父母危险因素-病例对照研究。
Pediatr Nephrol. 2023 Aug;38(8):2631-2641. doi: 10.1007/s00467-023-05900-6. Epub 2023 Feb 20.
7
Management of the congenital solitary kidney: consensus recommendations of the Italian Society of Pediatric Nephrology.先天性孤立肾的管理:意大利儿科学会肾脏病学分会的共识建议。
Pediatr Nephrol. 2022 Sep;37(9):2185-2207. doi: 10.1007/s00467-022-05528-y. Epub 2022 Jun 17.
8
Copy Number Variations Analysis Identifies QPRT as a Candidate Gene Associated With Susceptibility for Solitary Functioning Kidney.拷贝数变异分析确定QPRT为与孤立性功能肾易感性相关的候选基因。
Front Genet. 2021 May 17;12:575830. doi: 10.3389/fgene.2021.575830. eCollection 2021.
9
Robotic management of painful Zinner syndrome, case report and review of literature.疼痛性辛纳综合征的机器人手术治疗:病例报告及文献综述
Int J Surg Case Rep. 2020;73:61-64. doi: 10.1016/j.ijscr.2020.06.078. Epub 2020 Jun 22.
10
Genetics of the congenital absence of the vas deferens.先天性输精管缺失的遗传学研究。
Hum Genet. 2021 Jan;140(1):59-76. doi: 10.1007/s00439-020-02122-w. Epub 2020 Feb 5.