• 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

COVID-19 and hereditary spherocytosis: A recipe for hemolysis.

作者信息

Severance Tyler S, Rahim Mahvish Q, French James, Baker Richelle M, Shriner Andrew, Khaitan Alka, Overholt Kathleen M

机构信息

Riley Hospital for Children, Indianapolis, Indiana.

Indiana University School of Medicine, Indianapolis, Indiana.

出版信息

Pediatr Blood Cancer. 2021 Jan;68(1):e28548. doi: 10.1002/pbc.28548. Epub 2020 Jul 25.

DOI:10.1002/pbc.28548
PMID:32710684
Abstract
摘要

相似文献

1
COVID-19 and hereditary spherocytosis: A recipe for hemolysis.新冠病毒与遗传性球形红细胞增多症:溶血的诱因
Pediatr Blood Cancer. 2021 Jan;68(1):e28548. doi: 10.1002/pbc.28548. Epub 2020 Jul 25.
2
A flowchart strategy for children with leukemia during COVID-19: A nondesignated hospital's experience.
Pediatr Blood Cancer. 2021 Jan;68(1):e28563. doi: 10.1002/pbc.28563. Epub 2020 Jul 25.
3
Hereditary spherocytosis: Retrospective evaluation of 65 children.遗传性球形红细胞增多症:65例儿童的回顾性评估
Turk J Pediatr. 2018;60(3):264-269. doi: 10.24953/turkjped.2018.03.005.
4
Interaction of hereditary spherocytosis and alpha thalassaemia: a family study.遗传性球形红细胞增多症与α地中海贫血的相互作用:一项家族研究。
Acta Haematol. 1994;91(4):201-5. doi: 10.1159/000204335.
5
Inherited disorders of the red cell membrane skeleton.红细胞膜骨架的遗传性疾病。
Pediatr Clin North Am. 1980 May;27(2):463-86. doi: 10.1016/s0031-3955(16)33862-7.
6
CASE 5-2016Complex Congenital Cardiac Surgery in an Adult Patient With Hereditary Spherocytosis: Avoidance of Massive Hemolysis Associated With Extracorporeal Circulation in the Presence of Red Blood Cell Fragility.病例5-2016:一名患有遗传性球形红细胞增多症的成年患者的复杂先天性心脏手术:在存在红细胞脆性的情况下避免与体外循环相关的大量溶血。
J Cardiothorac Vasc Anesth. 2016 Jun;30(3):800-8. doi: 10.1053/j.jvca.2015.11.016. Epub 2015 Dec 1.
7
[Hereditary spherocytosis presenting with acute lymphoblastic leukemia].
Rinsho Ketsueki. 1987 Mar;28(3):402-7.
8
Hereditary spherocytosis with normal osmotic fragility after incubation. Is the autohemolysis test really obsolete?孵育后渗透脆性正常的遗传性球形红细胞增多症。自体溶血试验真的过时了吗?
JAMA. 1979 Jul 6;242(1):63-4.
9
Homozygous sickle cell disease with coexistent hereditary spherocytosis in three siblings.三名兄弟姐妹患有纯合子镰状细胞病并伴有遗传性球形红细胞增多症。
J Pediatr. 1972 Feb;80(2):235-42. doi: 10.1016/s0022-3476(72)80584-5.
10
[Hereditary spherocytosis].
Dtsch Med Wochenschr. 1994 Feb 4;119(5):165-6.

引用本文的文献

1
Transient erythroblastopenia of childhood after COVID-19 infection: a case report.儿童 COVID-19 感染后一过性幼红细胞减少症:病例报告。
Ital J Pediatr. 2024 Jul 29;50(1):131. doi: 10.1186/s13052-024-01700-2.
2
COVID-19 in patients with anemia and haematological malignancies: risk factors, clinical guidelines, and emerging therapeutic approaches.COVID-19 与贫血和血液系统恶性肿瘤患者:风险因素、临床指南和新兴治疗方法。
Cell Commun Signal. 2024 Feb 15;22(1):126. doi: 10.1186/s12964-023-01316-9.
3
Progression of hemolysis in a patient with hereditary spherocytosis after the second dose of COVID-19 mRNA vaccine: Correspondence.
一名遗传性球形红细胞增多症患者在接种第二剂新冠病毒mRNA疫苗后溶血进展:通信
Hum Vaccin Immunother. 2023 Dec 15;19(3):2286117. doi: 10.1080/21645515.2023.2286117. Epub 2023 Nov 22.
4
Hematologic manifestations of coronavirus disease 2019 in children: Case-series report and a review.2019年冠状病毒病在儿童中的血液学表现:病例系列报告及文献综述
Front Pediatr. 2022 Aug 16;10:935236. doi: 10.3389/fped.2022.935236. eCollection 2022.
5
Hemolytic anemia in COVID-19.COVID-19 相关溶血性贫血。
Ann Hematol. 2022 Sep;101(9):1887-1895. doi: 10.1007/s00277-022-04907-7. Epub 2022 Jul 8.
6
Associations and Disease-Disease Interactions of COVID-19 with Congenital and Genetic Disorders: A Comprehensive Review.COVID-19 与先天性和遗传疾病的关联及疾病间相互作用:全面综述。
Viruses. 2022 Apr 27;14(5):910. doi: 10.3390/v14050910.
7
Haemolytic anemia triggered by SARS-CoV-2 in patient with hereditary spherocytosis.新冠病毒引发的遗传性球形红细胞增多症患者的溶血性贫血。
Med Clin (Engl Ed). 2021 Oct 22;157(8):e304-e305. doi: 10.1016/j.medcle.2021.03.014. Epub 2021 Oct 5.
8
Haemolytic anemia triggered by SARS-CoV-2 in patient with hereditary spherocytosis.新冠病毒引发遗传性球形红细胞增多症患者的溶血性贫血。
Med Clin (Barc). 2021 Oct 22;157(8):e304-e305. doi: 10.1016/j.medcli.2021.03.023. Epub 2021 May 7.