• 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

WITHDRAWN: Clinical and Genetic Spectrum of Children with Primary Ciliary Dyskinesia in China.

作者信息

Guan Yuhong, Yang Haiming, Yao Xingfeng, Xu Hui, Liu Hui, Tang Xiaolei, Hao Chanjuan, Zhang Xiang, Zhao Shunying, Ge Wentong, Ni Xin

机构信息

Department of Respiratory Medicine, Beijing Children's Hospital, Capital Medical University; National Center for Children's Health; Beijing, China.

Department of Pathology, Beijing Children's Hospital, Capital Medical University; National Center for Children's Health, Beijing, China.

出版信息

Chest. 2020 Jul 3. doi: 10.1016/j.chest.2020.06.045.

DOI:10.1016/j.chest.2020.06.045
PMID:32622824
Abstract
摘要

相似文献

1
WITHDRAWN: Clinical and Genetic Spectrum of Children with Primary Ciliary Dyskinesia in China.撤稿:中国原发性纤毛运动障碍患儿的临床与基因谱
Chest. 2020 Jul 3. doi: 10.1016/j.chest.2020.06.045.
2
Clinical features and genetic spectrum of children with primary ciliary dyskinesia in central China: a referral center retrospective analysis.中国中部地区原发性纤毛运动障碍患儿的临床特征与基因谱:一项转诊中心的回顾性分析
Front Pharmacol. 2025 Jun 13;16:1526675. doi: 10.3389/fphar.2025.1526675. eCollection 2025.
3
An eye on the future for defeating hydrocephalus, ciliary dyskinesia-related hydrocephalus: review article.着眼于未来,攻克脑积水:睫状体运动障碍相关性脑积水综述。
Br J Neurosurg. 2022 Jun;36(3):329-339. doi: 10.1080/02688697.2022.2074373. Epub 2022 May 17.
4
Clinical and genetic spectrum of primary ciliary dyskinesia in Chinese patients: a systematic review.原发性纤毛运动障碍的临床和遗传学特征:系统综述。
Orphanet J Rare Dis. 2022 Jul 19;17(1):283. doi: 10.1186/s13023-022-02427-1.
5
Clinical, Genetic, Morphological and Functional Correlations in a Large Series of Patients with Primary Ciliary Dyskinesia: A Heterogeneous Disease with a Controversial Diagnosis.大量原发性纤毛运动障碍患者的临床、遗传、形态学和功能相关性:一种诊断存在争议的异质性疾病
Mol Diagn Ther. 2025 Jul 31. doi: 10.1007/s40291-025-00801-w.
6
The Association of Neonatal Respiratory Distress With Ciliary Ultrastructure and Genotype in Primary Ciliary Dyskinesia.原发性纤毛运动障碍中新生儿呼吸窘迫与纤毛超微结构及基因型的关联
Pediatr Pulmonol. 2025 May;60(5):e71091. doi: 10.1002/ppul.71091.
7
The patient's experience of primary ciliary dyskinesia: a systematic review.原发性纤毛运动障碍患者的经历:一项系统综述
Qual Life Res. 2017 Sep;26(9):2265-2285. doi: 10.1007/s11136-017-1564-y. Epub 2017 Mar 30.
8
Case Report: Identification of a novel hemizygous variant in a primary ciliary dyskinesia patient with dual ciliary and flagellar defects.病例报告:在一名患有双纤毛和鞭毛缺陷的原发性纤毛运动障碍患者中鉴定出一种新的半合子变体。
Front Med (Lausanne). 2025 Jun 25;12:1574684. doi: 10.3389/fmed.2025.1574684. eCollection 2025.
9
Treatment and outcomes of chronic rhinosinusitis in children with primary ciliary dyskinesia: where is the evidence? A qualitative systematic review.儿童原发性纤毛运动障碍的慢性鼻-鼻窦炎的治疗和结局:有何证据?一项定性系统评价。
Int Forum Allergy Rhinol. 2013 Dec;3(12):986-91. doi: 10.1002/alr.21227. Epub 2013 Oct 4.
10
CFAP300 Loss-of-Function Mutations with Primary Ciliary Dyskinesia: Evidence from Ex Vivo and ALI Cultures.CFAP300功能丧失突变与原发性纤毛运动障碍:来自体外和ALI培养的证据。
Int J Mol Sci. 2025 Aug 7;26(15):7655. doi: 10.3390/ijms26157655.

引用本文的文献

1
Ultrastructural Sperm Flagellum Defects in a Patient With Compound Heterozygous Mutations and Primary Ciliary Dyskinesia/.一名患有复合杂合突变和原发性纤毛运动障碍患者的超微结构精子鞭毛缺陷/。
Front Genet. 2020 Aug 28;11:974. doi: 10.3389/fgene.2020.00974. eCollection 2020.