• 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

Congenital nephrotic syndrome of Finnish type and other types of early familial nephrotic syndromes.

作者信息

Norio R

出版信息

Birth Defects Orig Artic Ser. 1974;10(4):69-72.

PMID:4470912
Abstract

Many types of nephrotic syndromes occur also in newborns and young infants. Among these, the congenital nephrotic syndrome of Finnish type has proved to be a distinct entity transmitted by an autosomal recessive gene. Landmarks for its delineation and separation from other, less well-known types are given.

摘要

相似文献

1
Congenital nephrotic syndrome of Finnish type and other types of early familial nephrotic syndromes.
Birth Defects Orig Artic Ser. 1974;10(4):69-72.
2
Congenital and infantile nephrotic syndromes.
Prog Clin Biol Res. 1989;305:179-92.
3
[Genetic heterogeneity and pathology of congenital nephrotic syndrome and its significance in prenatal diagnosis].
J Genet Hum. 1985 Jun;33(2):153-6.
4
Infantile nephrotic syndrome. Clinicopathological study of 11 cases.小儿肾病综合征。11例临床病理研究。
Isr J Med Sci. 1983 Jul;19(7):626-30.
5
Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach.意大利芬兰型先天性肾病综合征:一种分子学方法。
J Nephrol. 2002 Nov-Dec;15(6):696-702.
6
[Congenital and infantile nephrotic syndrome].
Nephrol Ther. 2005 Mar;1(1):63-70. doi: 10.1016/j.nephro.2005.03.001. Epub 2005 Apr 7.
7
Congenital nephrotic syndrome of the Finnish type is not associated with the Pax-2 gene despite the promising transgenic animal model.尽管有前景看好的转基因动物模型,但芬兰型先天性肾病综合征与Pax-2基因并无关联。
Genomics. 1994 Feb;19(3):570-2. doi: 10.1006/geno.1994.1109.
8
Congenital nephrotic syndrome: clinico-pathological heterogeneity and prenatal diagnosis.
Clin Nephrol. 1983 May;19(5):243-9.
9
Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.先天性肾病综合征中nephrin基因(NPHS1)的突变谱
Hum Mutat. 2001 May;17(5):368-73. doi: 10.1002/humu.1111.
10
[Congenital nephrotic syndrome - Finnish type].
Verh Dtsch Ges Pathol. 1982;66:307-11.