• 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

Laronidase desensitization during stem cell transplant in a child with Hurler syndrome.

作者信息

Rosenberg Jessica, Jhaveri Pooja, Kelbel Theodore

机构信息

Penn State Hershey College of Medicine, Penn State Hershey Medical Center, Hershey, Pennsylvania.

Division of Pediatric Allergy and Immunology, Penn State Hershey Medical Center, Hershey, Pennsylvania.

出版信息

Ann Allergy Asthma Immunol. 2016 Apr;116(4):377-8. doi: 10.1016/j.anai.2016.01.023. Epub 2016 Feb 23.

DOI:10.1016/j.anai.2016.01.023
PMID:26916445
Abstract
摘要

相似文献

1
Laronidase desensitization during stem cell transplant in a child with Hurler syndrome.在一名患有Hurler综合征的儿童进行干细胞移植期间进行拉罗尼酶脱敏治疗。
Ann Allergy Asthma Immunol. 2016 Apr;116(4):377-8. doi: 10.1016/j.anai.2016.01.023. Epub 2016 Feb 23.
2
Laronidase hypersensitivity and desensitization in type I mucopolysaccharidosis: a case report.I型黏多糖贮积症中拉罗尼酶超敏反应与脱敏治疗:一例报告
Pediatr Allergy Immunol. 2014 Aug;25(5):498-9. doi: 10.1111/pai.12209.
3
Enzyme replacement therapy in patients who have mucopolysaccharidosis I and are younger than 5 years: results of a multinational study of recombinant human alpha-L-iduronidase (laronidase).对年龄小于5岁的黏多糖贮积症I型患者进行酶替代疗法:重组人α-L-艾杜糖醛酸酶(拉罗尼酶)的一项多国研究结果
Pediatrics. 2007 Jul;120(1):e37-46. doi: 10.1542/peds.2006-2156. Epub 2007 Jun 4.
4
Clinical trial of laronidase in Hurler syndrome after hematopoietic cell transplantation.Hurler 综合征造血细胞移植后拉罗尼酶的临床试验。
Pediatr Res. 2020 Jan;87(1):104-111. doi: 10.1038/s41390-019-0541-2. Epub 2019 Aug 21.
5
Enzyme replacement therapy with laronidase (Aldurazyme(®)) for treating mucopolysaccharidosis type I.用拉罗尼酶(阿糖苷酶α(Aldurazyme(®)))进行酶替代疗法治疗I型黏多糖贮积症。
Cochrane Database Syst Rev. 2016 Apr 1;4:CD009354. doi: 10.1002/14651858.CD009354.pub4.
6
Enzyme replacement therapy with laronidase (Aldurazyme(®)) for treating mucopolysaccharidosis type I.用拉罗尼酶(阿糖苷酶α(商品名:Aldurazyme(®)))进行酶替代疗法治疗I型黏多糖贮积症。
Cochrane Database Syst Rev. 2013 Nov 21(11):CD009354. doi: 10.1002/14651858.CD009354.pub3.
7
Successful desensitization of elosulfase alfa-induced anaphylaxis in a pediatric patient with Morquio syndrome.成功脱敏治疗一名患有黏多糖贮积症IV型的儿科患者的阿加糖酶α诱导的过敏反应。
J Allergy Clin Immunol Pract. 2017 Jul-Aug;5(4):1156-1157. doi: 10.1016/j.jaip.2017.02.020.
8
Successful desensitization of a patient with Fabry disease with agalsidase beta (Fabrazyme) anaphylaxis after omalizumab pretreatment.在奥马珠单抗预处理后,对患有法布里病且出现β-半乳糖苷酶(法布赞)过敏反应的患者成功进行脱敏治疗。
Ann Allergy Asthma Immunol. 2021 Jan;126(1):96-98. doi: 10.1016/j.anai.2020.08.026. Epub 2020 Aug 29.
9
Combined enzyme replacement and haematopoietic stem cell transplantation in Hurler syndrome.黏多糖贮积症Ⅰ型中的联合酶替代疗法与造血干细胞移植
J Paediatr Child Health. 2009 Jul-Aug;45(7-8):469-72. doi: 10.1111/j.1440-1754.2009.01537.x.
10
Shortened desensitization leading to a 2-year enzyme replacement therapy with elosulfase alfa.缩短脱敏疗程,从而开始为期两年的阿加糖酶α酶替代疗法。
Ann Allergy Asthma Immunol. 2021 Aug;127(2):261-262. doi: 10.1016/j.anai.2021.04.040. Epub 2021 May 14.

引用本文的文献

1
Novel approach to idursulfase and laronidase desensitization in type 2 and type 1 S mucopolysaccharidosis (MPS).新型伊度沙酶和拉罗尼酶脱敏治疗 2 型和 1 型黏多糖贮积症(MPS)。
Orphanet J Rare Dis. 2022 Nov 3;17(1):402. doi: 10.1186/s13023-022-02556-7.