• 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

Congenital and Acquired Chronic Neutropenias: Challenges, Perspectives and Implementation of the EuNet-INNOCHRON Action.

作者信息

Papadaki Helen A, Mavroudi Irene, Almeida Antonio, Bux Juergen, Cichy Joanna, Dale David C, Donadieu Jean, Höglund Petter, Karanfilski Oliver, Mecucci Cristina, Palmblad Jan, Skokowa Julia, Stamatopoulos Kostas, Touw Ivo, Warren Alan J, Welte Karl, Zeidler Cornelia, Dufour Carlo

机构信息

Haemopoiesis Research Laboratory, School of Medicine, University of Crete; Department of Hematology, University Hospital of Heraklion, Crete, Greece.

Department of Hematology, Hospital da Luz Lisboa, Portugal.

出版信息

Hemasphere. 2020 Jun 8;4(3):e406. doi: 10.1097/HS9.0000000000000406. eCollection 2020 Jun.

DOI:10.1097/HS9.0000000000000406
PMID:32647804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7306309/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/7306309/277aabe55c10/hs9-4-e406-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/7306309/277aabe55c10/hs9-4-e406-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435e/7306309/277aabe55c10/hs9-4-e406-g001.jpg

相似文献

1
Congenital and Acquired Chronic Neutropenias: Challenges, Perspectives and Implementation of the EuNet-INNOCHRON Action.先天性和获得性慢性中性粒细胞减少症：EuNet-INNOCHRON行动的挑战、前景与实施
Hemasphere. 2020 Jun 8;4(3):e406. doi: 10.1097/HS9.0000000000000406. eCollection 2020 Jun.
2
European guidelines on treatment and supportive measures in chronic neutropenias: A consensus between the European Hematology Association and the EuNet-INNOCHRON COST Action based on a systematic evidence review.欧洲慢性中性粒细胞减少症治疗与支持措施指南：欧洲血液学协会与基于系统证据审查的EuNet-INNOCHRON成本行动之间的共识。
Hemasphere. 2025 Apr 16;9(4):e70113. doi: 10.1002/hem3.70113. eCollection 2025 Apr.
3
The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action.《欧洲成人及儿童中性粒细胞减少症诊断与管理指南：欧洲血液学协会与EuNet-INNOCHRON成本行动之间的共识》
Hemasphere. 2023 Mar 30;7(4):e872. doi: 10.1097/HS9.0000000000000872. eCollection 2023 Apr.
4
Correction Notice-The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action.勘误通知——《成人及儿童中性粒细胞减少症诊断与管理欧洲指南：欧洲血液学协会与EuNet-INNOCHRON COST行动之间的共识》
Hemasphere. 2023 Apr 27;7(5):e897. doi: 10.1097/HS9.0000000000000897. eCollection 2023 May.
5
Late-onset and long-lasting neutropenias in the young: A new entity anticipating immune-dysregulation disorders.儿童迟发性和持久性中性粒细胞减少症：一种预示免疫失调疾病的新实体。
Am J Hematol. 2024 Apr;99(4):534-542. doi: 10.1002/ajh.27221. Epub 2024 Jan 29.
6
The metabolic basis of inherited neutropenias.遗传性中性粒细胞减少症的代谢基础。
Br J Haematol. 2024 Jan;204(1):45-55. doi: 10.1111/bjh.19192. Epub 2023 Dec 4.
7
Perspectives of Challenges in Counseling for Congenital Heart Defects.先天性心脏病咨询中的挑战视角
Pediatr Cardiol. 2025 Apr;46(4):947-955. doi: 10.1007/s00246-024-03520-x. Epub 2024 Jun 22.
8
Hypopituitarism: genetic, developmental, and acquired etiologies with a focus on the emerging concept of autoimmune hypophysitis.垂体功能减退症：遗传、发育及后天病因，重点关注自身免疫性垂体炎这一新兴概念。
Endocr J. 2025 Jun 2;72(6):649-662. doi: 10.1507/endocrj.EJ25-0035. Epub 2025 Mar 27.
9
Defining next steps in the clinical implementation of polygenic scores: A landscape analysis of professional groups' perspectives.界定多基因评分临床应用的后续步骤：专业团体观点的全景分析
Genet Med. 2025 Jun;27(6):101414. doi: 10.1016/j.gim.2025.101414. Epub 2025 Mar 18.
10
Stakeholder Perspectives of Clinical Artificial Intelligence Implementation: Systematic Review of Qualitative Evidence.利益相关者对临床人工智能实施的观点：定性证据的系统评价。
J Med Internet Res. 2023 Jan 10;25:e39742. doi: 10.2196/39742.

引用本文的文献

1
The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action.《欧洲成人及儿童中性粒细胞减少症诊断与管理指南：欧洲血液学协会与EuNet-INNOCHRON成本行动之间的共识》
Hemasphere. 2023 Mar 30;7(4):e872. doi: 10.1097/HS9.0000000000000872. eCollection 2023 Apr.
2
Autoimmune Neutropenias: Update on Clinical and Biological Features in Children and Adults.自身免疫性中性粒细胞减少症：儿童和成人临床及生物学特征的最新进展
Hemasphere. 2022 Dec 19;7(1):e814. doi: 10.1097/HS9.0000000000000814. eCollection 2023 Jan.

本文引用的文献

1
Increased frequency of the single nucleotide polymorphism of the DARC/ACKR1 gene associated with ethnic neutropenia in a cohort of European patients with chronic idiopathic neutropenia.在一组患有慢性特发性中性粒细胞减少症的欧洲患者中，与种族性中性粒细胞减少相关的DARC/ACKR1基因单核苷酸多态性频率增加。
Am J Hematol. 2020 Jul;95(7):E163-E166. doi: 10.1002/ajh.25813. Epub 2020 Apr 17.
2
CRISPR/Cas9 Genome Editing of Human-Induced Pluripotent Stem Cells Followed by Granulocytic Differentiation.CRISPR/Cas9 基因组编辑的人类诱导多能干细胞，随后进行粒细胞分化。
Methods Mol Biol. 2020;2115:471-483. doi: 10.1007/978-1-0716-0290-4_27.
3
HSCT may lower leukemia risk in ELANE neutropenia: a before-after study from the French Severe Congenital Neutropenia Registry.
HSCT 可能降低 ELANE 中性粒细胞减少症的白血病风险：来自法国严重先天性中性粒细胞减少症登记处的前后研究。
Bone Marrow Transplant. 2020 Aug;55(8):1614-1622. doi: 10.1038/s41409-020-0800-1. Epub 2020 Jan 28.
4
Registries for study of nonmalignant hematological diseases: the example of the Severe Chronic Neutropenia International Registry.研究非恶性血液病的登记处：以严重慢性中性粒细胞减少症国际登记处为例。
Curr Opin Hematol. 2020 Jan;27(1):18-26. doi: 10.1097/MOH.0000000000000558.
5
Myeloid-Derived Suppressor Cells in Hematologic Diseases: Promising Biomarkers and Treatment Targets.血液系统疾病中的髓源性抑制细胞：有前景的生物标志物和治疗靶点
Hemasphere. 2019 Jan 28;3(1):e168. doi: 10.1097/HS9.0000000000000168. eCollection 2019 Feb.
6
CRISPR/Cas9-mediated knockout enables neutrophilic maturation of primary hematopoietic stem and progenitor cells and induced pluripotent stem cells of severe congenital neutropenia patients.CRISPR/Cas9 介导的基因敲除可使严重先天性中性粒细胞减少症患者的原代造血干/祖细胞和诱导多能干细胞向中性粒细胞成熟。
Haematologica. 2020 Mar;105(3):598-609. doi: 10.3324/haematol.2019.221804. Epub 2019 Jun 27.
7
Ethnic benign neutropenia: A phenomenon finds an explanation.遗传性良性中性粒细胞减少症：现象有了合理解释。
Pediatr Blood Cancer. 2018 Dec;65(12):e27361. doi: 10.1002/pbc.27361. Epub 2018 Aug 16.
8
Clinical features and therapeutic challenges of cytopenias belonging to alps and alps-related (ARS) phenotype.属于自身免疫性淋巴细胞增生综合征（ALPS）及ALPS相关（ARS）表型的血细胞减少症的临床特征及治疗挑战
Br J Haematol. 2019 Mar;184(5):861-864. doi: 10.1111/bjh.15178. Epub 2018 Mar 12.
9
Molecular basis of the human ribosomopathy Shwachman-Diamond syndrome.人类核糖体病施瓦赫曼-戴蒙德综合征的分子基础。
Adv Biol Regul. 2018 Jan;67:109-127. doi: 10.1016/j.jbior.2017.09.002. Epub 2017 Sep 6.
10
Congenital neutropenia in the era of genomics: classification, diagnosis, and natural history.基因组学时代的先天性中性粒细胞减少症：分类、诊断及自然病史
Br J Haematol. 2017 Nov;179(4):557-574. doi: 10.1111/bjh.14887. Epub 2017 Sep 6.