• 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 Type 1 and 2 in Finland: Incidence, Prevalence, and Preceding Diagnoses.

作者信息

Sandberg Andreas, Lassenius Mariann, Vihervaara Ville, Toppila Iiro, Huilaja Laura

机构信息

Takeda Oy, Helsinki, Finland.

Medaffcon Oy, Espoo, Finland.

出版信息

Acta Derm Venereol. 2024 May 6;104:adv24176. doi: 10.2340/actadv.v104.24176.

DOI:10.2340/actadv.v104.24176
PMID:38708992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11091904/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5d9/11091904/aef420e6917b/ActaDV-104-24176-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5d9/11091904/aef420e6917b/ActaDV-104-24176-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5d9/11091904/aef420e6917b/ActaDV-104-24176-g001.jpg

相似文献

1
Hereditary Angioedema Type 1 and 2 in Finland: Incidence, Prevalence, and Preceding Diagnoses.芬兰1型和2型遗传性血管性水肿:发病率、患病率及既往诊断情况
Acta Derm Venereol. 2024 May 6;104:adv24176. doi: 10.2340/actadv.v104.24176.
2
Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations.携带错义C1INH基因突变的遗传性血管性水肿患者的临床表现较轻。
J Allergy Clin Immunol. 2013 Jun;131(6):1708-11. doi: 10.1016/j.jaci.2012.11.015. Epub 2012 Dec 23.
3
Association of celiac disease and hereditary angioedema due to C1-inhibitor deficiency. Screening patients with hereditary angioedema for celiac disease: is it worth the effort?乳糜泻与 C1 酯酶抑制剂缺乏引起的遗传性血管性水肿的相关性。对遗传性血管性水肿患者进行乳糜泻筛查:是否值得付出努力?
Eur J Gastroenterol Hepatol. 2011 Mar;23(3):238-44. doi: 10.1097/MEG.0b013e328343d3b2.
4
[Hereditary angioedema in Medellín (Colombia): Clinical evaluation and quality of life appraisal].[麦德林(哥伦比亚)的遗传性血管性水肿:临床评估与生活质量评价]
Biomedica. 2015 Jul-Sep;35(3):419-28. doi: 10.7705/biomedica.v35i3.2417.
5
Pregnancy and Postpartum in Hereditary Angioedema With C1 Inhibitor Deficit in Women Who Have No Access to Therapy.
J Investig Allergol Clin Immunol. 2017;27(5):322-323. doi: 10.18176/jiaci.0175.
6
Hereditary angioedema: 44 years of diagnostic delay.遗传性血管性水肿:44年的诊断延误。
Dermatol Online J. 2016 Apr 18;22(4):13030/qt5cf802wr.
7
Complement Study Versus CINH Gene Testing for the Diagnosis of Type I Hereditary Angioedema in Children.补体研究与C1INH基因检测在儿童I型遗传性血管性水肿诊断中的比较
J Clin Immunol. 2016 Jan;36(1):16-8. doi: 10.1007/s10875-015-0222-9. Epub 2015 Dec 10.
8
Chronic spontaneous urticaria and angioedema requiring treatment with omalizumab in a patient with hereditary angioedema.遗传性血管性水肿患者慢性自发性荨麻疹和血管性水肿需用奥马珠单抗治疗
Ann Allergy Asthma Immunol. 2019 Jun;122(6):666-667. doi: 10.1016/j.anai.2019.02.019. Epub 2019 Mar 1.
9
[Hereditary angioedema. Family history and clinical manifestations in 58 patients].[遗传性血管性水肿。58例患者的家族史和临床表现]
Medicina (B Aires). 2009;69(6):601-6.
10
Acute Pancreatitis in the Context of Abdominal Attack of Hereditary Angioedema.遗传性血管性水肿腹部发作情况下的急性胰腺炎
J Investig Allergol Clin Immunol. 2020 Aug;30(4):281-283. doi: 10.18176/jiaci.0490.

引用本文的文献

1
Hereditary angioedema diagnosis: Reflecting on the past, envisioning the future.遗传性血管性水肿的诊断:回顾过去,展望未来。
World Allergy Organ J. 2025 May 14;18(6):101060. doi: 10.1016/j.waojou.2025.101060. eCollection 2025 Jun.

本文引用的文献

1
Accurate diagnosis of bullous pemphigoid requires multiple health care visits.大疱性类天疱疮的准确诊断需要多次就诊。
Front Immunol. 2023 Nov 27;14:1281302. doi: 10.3389/fimmu.2023.1281302. eCollection 2023.
2
Validation of Diagnoses of Atopic Dermatitis in Hospital Registries: A Cross-sectional Database Study from Finland.医院登记处中特应性皮炎诊断的验证:一项来自芬兰的横断面数据库研究
Acta Derm Venereol. 2023 Jul 10;103:adv7266. doi: 10.2340/actadv.v103.7266.
3
Hyperhidrosis Comorbidities and Treatments: A Register-based Study among 511 Subjects.
多汗症合并症及其治疗:511 例受试者的基于登记的研究。
Acta Derm Venereol. 2022 Feb 28;102:adv00656. doi: 10.2340/actadv.v102.1061.
4
The international WAO/EAACI guideline for the management of hereditary angioedema-The 2021 revision and update.《遗传性血管性水肿管理的国际 WAO/EAACI 指南-2021 年修订版》。
Allergy. 2022 Jul;77(7):1961-1990. doi: 10.1111/all.15214. Epub 2022 Feb 3.
5
Hereditary angioedema: Epidemiology and burden of disease.遗传性血管性水肿:流行病学和疾病负担。
Allergy Asthma Proc. 2020 Nov 1;41(Suppl 1):S08-S13. doi: 10.2500/aap.2020.41.200050.
6
Validation of Psoriasis Diagnoses Recorded in Finnish Biobanks.芬兰生物样本库中记录的银屑病诊断的验证
Acta Derm Venereol. 2020 Oct 21;100(17):adv00297. doi: 10.2340/00015555-3656.
7
US HAEA Medical Advisory Board 2020 Guidelines for the Management of Hereditary Angioedema.美国遗传性血管性水肿学会医学顾问委员会 2020 年遗传性血管性水肿管理指南。
J Allergy Clin Immunol Pract. 2021 Jan;9(1):132-150.e3. doi: 10.1016/j.jaip.2020.08.046. Epub 2020 Sep 6.
8
Comorbidities of Alopecia Areata in Finland between 1987 and 2016.1987年至2016年间芬兰斑秃的合并症
Acta Derm Venereol. 2020 Feb 25;100(4):adv00063. doi: 10.2340/00015555-3412.
9
Improvement in diagnostic delays over time in patients with hereditary angioedema: findings from the Icatibant Outcome Survey.遗传性血管性水肿患者诊断延迟随时间的改善:依库珠单抗疗效调查结果
Clin Transl Allergy. 2018 Oct 12;8:42. doi: 10.1186/s13601-018-0229-4. eCollection 2018.
10
Epidemiology of Bradykinin-mediated angioedema: a systematic investigation of epidemiological studies.缓激肽介导的血管性水肿的流行病学:对流行病学研究的系统调查。
Orphanet J Rare Dis. 2018 May 4;13(1):73. doi: 10.1186/s13023-018-0815-5.