• 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

Stealth thrombosis of brain and kidney in a girl with Upshaw-Schulman syndrome not receiving prophylactic plasma infusions.

作者信息

Tanabe Saori, Fujimura Yoshihiro, Lämmle Bernhard, Kimura Toshiyuki, Isonishi Ayami, Sakai Kazuya, Matsumoto Masanori

机构信息

Department of Pediatrics, Nihonkai General Hospital, Sakata, Japan.

Japanese Red Cross Kinki Block Blood Center, Osaka, Japan.

出版信息

Int J Hematol. 2020 Nov;112(5):603-604. doi: 10.1007/s12185-020-02997-5. Epub 2020 Sep 23.

DOI:10.1007/s12185-020-02997-5
PMID:32965638
Abstract
摘要

相似文献

1
Stealth thrombosis of brain and kidney in a girl with Upshaw-Schulman syndrome not receiving prophylactic plasma infusions.
Int J Hematol. 2020 Nov;112(5):603-604. doi: 10.1007/s12185-020-02997-5. Epub 2020 Sep 23.
2
Epidemiology and pathophysiology of adulthood-onset thrombotic microangiopathy with severe ADAMTS13 deficiency (thrombotic thrombocytopenic purpura): a cross-sectional analysis of the French national registry for thrombotic microangiopathy.伴有严重ADAMTS13缺乏的成人期血栓性微血管病(血栓性血小板减少性紫癜)的流行病学和病理生理学:法国全国血栓性微血管病登记处的横断面分析
Lancet Haematol. 2016 May;3(5):e237-45. doi: 10.1016/S2352-3026(16)30018-7. Epub 2016 Apr 16.
3
Upshaw-Schulman Syndrome With c.2728C>T Mutation in ADAMTS13 Gene.伴有ADAMTS13基因c.2728C>T突变的厄普肖-舒尔曼综合征
J Pediatr Hematol Oncol. 2019 Jan;41(1):e60-e62. doi: 10.1097/MPH.0000000000001226.
4
Desmopressin, an unexpected link between nocturnal enuresis and inherited thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).去氨加压素,夜间遗尿症与遗传性血栓性血小板减少性紫癜(乌-舒二氏综合征)之间的一种意外关联。
J Thromb Haemost. 2006 Mar;4(3):700-1. doi: 10.1111/j.1538-7836.2005.01768.x.
5
Upshaw-Schulman syndrome and pregnancy: successful management with plasma infusions.昂肖-舒尔曼综合征与妊娠:血浆输注治疗成功案例
Ann Hematol. 2016 Oct;95(10):1745-6. doi: 10.1007/s00277-016-2755-2. Epub 2016 Jul 25.
6
Congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) caused by novel ADAMTS13 mutations.由新型ADAMTS13突变引起的先天性血栓性血小板减少性紫癜(Upshaw-Schulman综合征)。
Br J Haematol. 2016 Apr;173(1):156-9. doi: 10.1111/bjh.13564. Epub 2015 Jun 18.
7
Severe Hemolysis and Pulmonary Hypertension in a Neonate With Upshaw-Schulman Syndrome.患有厄普肖-舒尔曼综合征的新生儿出现严重溶血和肺动脉高压
Pediatrics. 2016 Dec;138(6). doi: 10.1542/peds.2016-1565.
8
Experiences in a family with the Upshaw-Schulman syndrome over a 44-year period.44 年间一个 Upshaw-Schulman 综合征家系的诊治经验。
Clin Appl Thromb Hemost. 2014 Apr;20(3):296-303. doi: 10.1177/1076029613495309. Epub 2013 Jul 19.
9
Current prophylactic plasma infusion protocols do not adequately prevent long-term cumulative organ damage in the Japanese congenital thrombotic thrombocytopenic purpura cohort.目前的预防性血浆输注方案并不能充分预防日本先天性血栓性血小板减少性紫癜队列的长期累积性器官损伤。
Br J Haematol. 2021 Jul;194(2):444-452. doi: 10.1111/bjh.17560. Epub 2021 May 28.
10
Complement activation associated with ADAMTS13 deficiency may contribute to the characteristic glomerular manifestations in Upshaw-Schulman syndrome.补体激活与 ADAMTS13 缺乏相关,可能导致 Ussawa-Schulman 综合征的特征性肾小球表现。
Thromb Res. 2018 Oct;170:148-155. doi: 10.1016/j.thromres.2018.08.020. Epub 2018 Sep 1.

引用本文的文献

1
Diagnosis of Hereditary TTP Caused by Homozygosity for a Rare Complex ADAMTS13 Allele After Salmonella Infection in a 43-Year-Old Asylum Seeker.一名43岁寻求庇护者在感染沙门氏菌后,因罕见的复合ADAMTS13等位基因纯合性导致遗传性血栓性血小板减少性紫癜的诊断。
Front Med (Lausanne). 2021 Feb 26;8:639441. doi: 10.3389/fmed.2021.639441. eCollection 2021.