• 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

Utility of platelet cross-matching in a case of neonatal alloimmune thrombocytopenia associated with a de novo MECOM variant.

作者信息

Datta Suvro Sankha, Basu Sabita, Ghara Niharendu, Kole Pulak, Khemka Priti

机构信息

Department of Transfusion Medicine, Tata Medical Center, Rajarhat, India.

Department of Pediatric Hematology, Tata Medical Center, Rajarhat, India.

出版信息

Blood Res. 2021 Mar 31;56(1):53-56. doi: 10.5045/br.2021.2020299.

DOI:10.5045/br.2021.2020299
PMID:33542165
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7987477/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ae/7987477/afb7417df9f3/br-56-1-53-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ae/7987477/afb7417df9f3/br-56-1-53-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ae/7987477/afb7417df9f3/br-56-1-53-f1.jpg

相似文献

1
Utility of platelet cross-matching in a case of neonatal alloimmune thrombocytopenia associated with a de novo MECOM variant.血小板交叉配型在一例与新发MECOM变异相关的新生儿同种免疫性血小板减少症中的应用
Blood Res. 2021 Mar 31;56(1):53-56. doi: 10.5045/br.2021.2020299.
2
Neonatal alloimmune thrombocytopenia: antenatal management.新生儿同种免疫性血小板减少症：产前管理
Am J Obstet Gynecol. 2000 May;182(5):1233-8. doi: 10.1067/mob.2000.104841.
3
[Neonatal alloimmune thrombocytopenia with hemorrhagic infarction of the right hemisphere].[新生儿同种免疫性血小板减少症伴右侧半球出血性梗死]
Z Geburtshilfe Neonatol. 2002 Jan-Feb;206(1):26-9. doi: 10.1055/s-2002-20948.
4
Perinatal management of neonatal alloimmune thrombocytopenia associated with anti-group A antibody.与抗A组抗体相关的新生儿同种免疫性血小板减少症的围产期管理
Transfus Med. 2015 Feb;25(1):42-6. doi: 10.1111/tme.12178. Epub 2015 Mar 6.
5
MYH9-macrothrombocytopenia caused by a novel variant (E1421K) initially presenting as apparent neonatal alloimmune thrombocytopenia.由新型变异（E1421K）引起的 MYH9-巨血小板减少症，最初表现为明显的新生儿同种免疫性血小板减少症。
Pediatr Blood Cancer. 2018 Apr;65(4). doi: 10.1002/pbc.26949. Epub 2017 Dec 29.
6
Omission of fetal sampling in treatment of subsequent pregnancies in fetal-neonatal alloimmune thrombocytopenia.胎儿 - 新生儿同种免疫性血小板减少症后续妊娠治疗中胎儿采样的省略
Am J Obstet Gynecol. 2016 Oct;215(4):471.e1-9. doi: 10.1016/j.ajog.2016.04.033. Epub 2016 Apr 27.
7
Differential diagnosis of neonatal alloimmune thrombocytopenia: Type 2B von Willebrand disease.新生儿同种免疫性血小板减少症的鉴别诊断：2B 型血管性血友病。
Platelets. 2017 Dec;28(8):825-828. doi: 10.1080/09537104.2017.1293811. Epub 2017 Apr 24.
8
Alloimmune thrombocytopenia of the fetus and the newborn.胎儿及新生儿同种免疫性血小板减少症
Blood Rev. 2002 Mar;16(1):69-72. doi: 10.1054/blre.2001.0187.
9
Antiendothelial αvβ3 Antibodies Are a Major Cause of Intracranial Bleeding in Fetal/Neonatal Alloimmune Thrombocytopenia.抗内皮αvβ3抗体是胎儿/新生儿同种免疫性血小板减少症颅内出血的主要原因。
Arterioscler Thromb Vasc Biol. 2016 Aug;36(8):1517-24. doi: 10.1161/ATVBAHA.116.307281. Epub 2016 Jun 9.
10
Fetal/neonatal alloimmune thrombocytopenia due to anti-CD36 antibodies: antibody evaluations by CD36-transfected cell lines.抗CD36抗体所致胎儿/新生儿同种免疫性血小板减少症：通过CD36转染细胞系进行抗体评估
Transfusion. 2018 Jan;58(1):189-195. doi: 10.1111/trf.14369. Epub 2017 Oct 13.

引用本文的文献

1
A novel MECOM gene variant causes severe thrombocytopenia in a neonate: a case report and review of the literature.一种新型MECOM基因变异导致新生儿严重血小板减少症：病例报告及文献综述
J Med Case Rep. 2025 Apr 1;19(1):147. doi: 10.1186/s13256-025-05194-2.
2
A novel missense mutation in the MECOM gene in a Chinese boy with radioulnar synostosis with amegakaryocytic thrombocytopenia.一个患有桡尺骨融合伴巨核细胞减少性血小板减少症的中国男孩中 MECOM 基因的新型错义突变。
BMC Pediatr. 2024 Jan 20;24(1):62. doi: 10.1186/s12887-024-04552-1.
3
Mecom mutation related to radioulnar synostosis with amegakaryocytic thrombocytopenia reduces HSPCs in mice.

本文引用的文献

1
MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia.MECOM 相关综合征：一种具有巨核细胞减少性血小板减少症的异质性遗传性骨髓衰竭综合征。
Blood Adv. 2018 Mar 27;2(6):586-596. doi: 10.1182/bloodadvances.2018016501.
2
How do I … manage the platelet transfusion-refractory patient?我该如何……管理血小板输注难治性患者？
Transfusion. 2017 Dec;57(12):2828-2835. doi: 10.1111/trf.14316. Epub 2017 Sep 28.
3
Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia.
Mecom 突变与桡尺骨融合伴巨核细胞血小板减少症有关，导致小鼠 HSPC 减少。
Blood Adv. 2023 Sep 26;7(18):5409-5420. doi: 10.1182/bloodadvances.2022008462.
编码癌蛋白EVI1的MECOM基因突变导致桡尺骨融合伴无巨核细胞性血小板减少症。
Am J Hum Genet. 2015 Dec 3;97(6):848-54. doi: 10.1016/j.ajhg.2015.10.010. Epub 2015 Nov 12.
4
Human platelet antigens - 2013.人类血小板抗原 - 2013.
Vox Sang. 2014 Feb;106(2):93-102. doi: 10.1111/vox.12085. Epub 2013 Sep 16.
5
Neonatal alloimmune thrombocytopenia: pathogenesis, diagnosis and management.新生儿同种免疫性血小板减少症：发病机制、诊断与治疗。
Br J Haematol. 2013 Apr;161(1):3-14. doi: 10.1111/bjh.12235. Epub 2013 Feb 6.
6
A screening and intervention program aimed to reduce mortality and serious morbidity associated with severe neonatal alloimmune thrombocytopenia.一项旨在降低与严重新生儿同种免疫性血小板减少症相关的死亡率和严重发病率的筛查与干预计划。
Blood. 2007 Aug 1;110(3):833-9. doi: 10.1182/blood-2006-08-040121. Epub 2007 Apr 11.
7
Frequencies of maternal platelet alloantibodies and autoantibodies in suspected fetal/neonatal alloimmune thrombocytopenia, with emphasis on human platelet antigen-15 alloimmunization.疑似胎儿/新生儿同种免疫性血小板减少症中母体血小板同种抗体和自身抗体的频率，重点关注人类血小板抗原-15同种免疫
Vox Sang. 2005 Jul;89(1):39-43. doi: 10.1111/j.1423-0410.2005.00662.x.
8
Transfusion guidelines for neonates and older children.新生儿和大龄儿童输血指南。
Br J Haematol. 2004 Feb;124(4):433-53. doi: 10.1111/j.1365-2141.2004.04815.x.