• 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

Hereditary Angioedema.

作者信息

Busse Paula J, Christiansen Sandra C

机构信息

From the Division of Clinical Immunology and Allergy, Icahn School of Medicine at Mount Sinai, New York (P.J.B.); and the Department of Medicine, University of California, San Diego, San Diego (S.C.C.).

出版信息

N Engl J Med. 2020 Mar 19;382(12):1136-1148. doi: 10.1056/NEJMra1808012.

DOI:10.1056/NEJMra1808012
PMID:32187470
Abstract
摘要

相似文献

1
Hereditary Angioedema.遗传性血管性水肿
N Engl J Med. 2020 Mar 19;382(12):1136-1148. doi: 10.1056/NEJMra1808012.
2
Hereditary angioedema: a clinical review for the otolaryngologist.遗传性血管性水肿：耳鼻咽喉科医生的临床综述
Ear Nose Throat J. 2011 Jan;90(1):32-9. doi: 10.1177/014556131109000822.
3
Effectiveness of lanadelumab in patients with hereditary angioedema with normal C1 inhibitor and FXII mutation.拉那度单抗在C1抑制剂正常且存在FXII突变的遗传性血管性水肿患者中的疗效。
Ann Allergy Asthma Immunol. 2021 Sep;127(3):391-392. doi: 10.1016/j.anai.2021.05.028. Epub 2021 May 31.
4
Management of pregnancies in a hereditary angioedema patient after treatment with attenuated androgens since childhood.自童年起接受减毒雄激素治疗的遗传性血管性水肿患者的妊娠管理。
J Obstet Gynaecol. 2015 Jan;35(1):89-90. doi: 10.3109/01443615.2014.925860. Epub 2014 Jun 12.
5
Efficacy of lanadelumab in angioedema due to acquired C1 inhibitor deficiency.拉那度单抗治疗获得性C1抑制物缺乏所致血管性水肿的疗效。
J Allergy Clin Immunol Pract. 2023 Mar;11(3):963-965.e1. doi: 10.1016/j.jaip.2022.10.041. Epub 2022 Nov 13.
6
New hope for those with hereditary angioedema.遗传性血管性水肿患者的新希望。
Nursing. 2012 Apr;42(4):43-6. doi: 10.1097/01.NURSE.0000410311.38734.a9.
7
Evaluation of the safety and effectiveness of berotralstat for patients with hereditary angioedema: Report of six cases.贝罗他司特对遗传性血管性水肿患者安全性和有效性的评估：6例报告
J Dermatol. 2023 Nov;50(11):1506-1508. doi: 10.1111/1346-8138.16965. Epub 2023 Sep 18.
8
The natural history of hereditary angioedema and the impact of treatment with human C1-inhibitor concentrate during pregnancy: a long-term survey.遗传性血管性水肿的自然病史和人 C1 抑制剂浓缩物在妊娠期间治疗的影响：一项长期调查。
Eur J Obstet Gynecol Reprod Biol. 2010 Sep;152(1):44-9. doi: 10.1016/j.ejogrb.2010.05.008. Epub 2010 Jun 11.
9
Recurrent angio-oedema--three cases of C1 inhibitor deficiency.复发性血管性水肿——3例C1抑制剂缺乏症
J Assoc Physicians India. 2013 Dec;61(12):927-30.
10
A recombinant C1 esterase inhibitor (Ruconest) for hereditary angioedema.一种用于遗传性血管性水肿的重组C1酯酶抑制剂（Ruconest）。
Med Lett Drugs Ther. 2016 Mar 28;58(1491):e44-5.

引用本文的文献

1
Three-year real-world outcomes of lanadelumab prophylaxis in hereditary angioedema: Complete disease suppression and psychosocial benefits in two East Asian patients.遗传性血管性水肿患者使用lanadelumab预防治疗的三年真实世界疗效：两名东亚患者实现疾病完全抑制并获得心理社会益处
Intractable Rare Dis Res. 2025 Aug 31;14(3):210-215. doi: 10.5582/irdr.2025.01045.
2
Expanding the Genetic and Clinical Spectrum of Hereditary Angioedema with Normal C1 Inhibitor: Novel Variants and Treatment Insights.扩大C1抑制剂正常的遗传性血管性水肿的遗传和临床谱：新变异及治疗见解
J Clin Immunol. 2025 Aug 23;45(1):124. doi: 10.1007/s10875-025-01912-z.
3
Proactive identification of rare diseases: lessons from hereditary angioedema diagnosis using electronic medical records.
罕见病的主动识别：利用电子病历进行遗传性血管性水肿诊断的经验教训。
Orphanet J Rare Dis. 2025 Jul 28;20(1):386. doi: 10.1186/s13023-025-03882-2.
4
Activation of the Complement/Lectin Pathway, Angiopoietin/Tie-2/VEGF-System, Cytokines and Chemokines in Different Angioedema Subtypes.不同血管性水肿亚型中补体/凝集素途径、血管生成素/Tie-2/血管内皮生长因子系统、细胞因子和趋化因子的激活
Eur J Immunol. 2025 Jul;55(7):e70010. doi: 10.1002/eji.70010.
5
Case reports of subcutaneous pdC1INH in pregnancy and lactation: expanding treatment options for hereditary angioedema in Portugal.孕期及哺乳期皮下注射C1酯酶抑制剂的病例报告：拓展葡萄牙遗传性血管性水肿的治疗选择
Front Allergy. 2025 Jul 2;6:1604440. doi: 10.3389/falgy.2025.1604440. eCollection 2025.
6
[Not Available].[无可用内容]
CMAJ. 2025 Jul 1;197(24):E703-E704. doi: 10.1503/cmaj.241815-f.
7
A Two-Decade-Delayed Diagnosis of Hereditary Angioedema: A Case Report.遗传性血管性水肿延迟二十年的诊断：一例报告
Cureus. 2025 May 29;17(5):e85019. doi: 10.7759/cureus.85019. eCollection 2025 May.
8
C1 inhibitor deficient hereditary angioedema is related to endothelial dysfunction in young adult and middle-aged patients.C1 抑制剂缺乏遗传性血管性水肿与年轻及中年患者的内皮功能障碍有关。
Clin Transl Allergy. 2025 Jun;15(6):e70076. doi: 10.1002/clt2.70076.
9
Reductions in medical visits and hospitalizations following berotralstat initiation in patients with hereditary angioedema in the United States.在美国，遗传性血管性水肿患者开始使用贝罗司他后，医疗就诊次数和住院次数减少。
J Manag Care Spec Pharm. 2025 Jun;31(6):578-589. doi: 10.18553/jmcp.2025.31.6.578.
10
Th2 predominance and decreased NK cells in patients with hereditary angioedema.遗传性血管性水肿患者中Th2优势及自然杀伤细胞减少
Front Immunol. 2025 May 14;16:1536128. doi: 10.3389/fimmu.2025.1536128. eCollection 2025.