• 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

Late onset congenital adrenal hyperplasia: a gynecologist's perspective.

作者信息

Brodie B L, Wentz A C

出版信息

Fertil Steril. 1987 Aug;48(2):175-88. doi: 10.1016/s0015-0282(16)59339-x.

DOI:10.1016/s0015-0282(16)59339-x
PMID:3038624
Abstract
摘要

相似文献

1
Late onset congenital adrenal hyperplasia: a gynecologist's perspective.迟发性先天性肾上腺增生症:妇科医生的观点
Fertil Steril. 1987 Aug;48(2):175-88. doi: 10.1016/s0015-0282(16)59339-x.
2
Late onset congenital adrenal hyperplasia in a Puerto Rican family: hormonal and HLA typing.
Bol Asoc Med P R. 1986 Nov;78(11):472-6.
3
Late-onset adrenal hyperplasia.
N Engl J Med. 1986 Feb 13;314(7):450-1. doi: 10.1056/NEJM198602133140718.
4
A case of late-onset congenital adrenal hyperplasia due to partial 3 beta-hydroxysteroid dehydrogenase deficiency.一例因部分3β-羟基类固醇脱氢酶缺乏导致的迟发性先天性肾上腺皮质增生症。
Endocr J. 1993 Feb;40(1):107-9. doi: 10.1507/endocrj.40.107.
5
Congenital adrenal hyperplasia.
Clin Endocrinol Metab. 1985 Nov;14(4):893-909. doi: 10.1016/s0300-595x(85)80082-7.
6
[Congenital adrenal hyperplasia due to 3beta-hydroxysteroid dehydrogenase deficiency].[3β-羟类固醇脱氢酶缺乏所致先天性肾上腺皮质增生症]
Vnitr Lek. 2006 Oct;52(10):957-62.
7
Late onset adrenal hyperplasia (21-hydroxylase deficiency): 17-OH progesterone response to ACTH stimulation and HLA typing. A family study.迟发性肾上腺增生(21-羟化酶缺乏症):17-羟孕酮对促肾上腺皮质激素刺激的反应及人类白细胞抗原分型。一项家系研究。
Horm Res. 1981;14(2):73-8. doi: 10.1159/000179363.
8
Congenital adrenal hyperplasia: from genetics and biochemistry to clinical practice, Part 1.先天性肾上腺皮质增生症:从遗传学、生物化学到临床实践,第1部分
Clin Pediatr (Phila). 2001 Jan;40(1):1-16. doi: 10.1177/000992280104000101.
9
Congenital adrenal hyperplasia.
Clin Biochem. 1981 Oct;14(5):258-72. doi: 10.1016/s0009-9120(81)90988-7.
10
A new inherited variant of the 3 beta-hydroxysteroid dehydrogenase-isomerase deficiency syndrome: evidence for the existence of two isoenzymes.
J Clin Endocrinol Metab. 1986 Aug;63(2):360-7. doi: 10.1210/jcem-63-2-360.

引用本文的文献

1
Variations in the 3'UTR of the Gene in Heterozygous Females with Hyperandrogenaemia.患有高雄激素血症的杂合子女性中该基因3'非翻译区的变异
Int J Endocrinol. 2017;2017:8984365. doi: 10.1155/2017/8984365. Epub 2017 Apr 12.
2
Non-Classical Congenital Adrenal Hyperplasia in Childhood.儿童非经典型先天性肾上腺皮质增生症
J Clin Res Pediatr Endocrinol. 2017 Mar 1;9(1):1-7. doi: 10.4274/jcrpe.3378. Epub 2016 Jun 29.
3
21-Hydroxylase deficiency: from molecular genetics to clinical presentation.21-羟化酶缺乏症:从分子遗传学至临床表现
J Endocrinol Invest. 2005 Feb;28(2):187-92. doi: 10.1007/BF03345366.
4
New reliable biochemical marker for screening 21 alpha-hydroxylase deficiency without index person among hirsute women in agreement with HLA-haplotyping.一种新的可靠生化标志物,用于在多毛女性中筛查21α-羟化酶缺乏症,无需索引病例,且与HLA单倍型分型结果一致。
J Endocrinol Invest. 1995 Nov;18(10):754-61. doi: 10.1007/BF03349807.
5
Adrenal insufficiency in a man with non-classical 21-hydroxylase deficiency: consequence or coincidence?
J Endocrinol Invest. 1994 Sep;17(8):665-70. doi: 10.1007/BF03349683.
6
Late-onset congenital adrenal hyperplasia in a group of hyperandrogenic women.
Arch Gynecol Obstet. 1991;249(4):165-71. doi: 10.1007/BF02390383.