• 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

Further evidence for an association between LCI and FEV1 in patients with PCD.

作者信息

Nyilas Sylvia, Schlegtendal Anne, Yammine Sophie, Casaulta Carmen, Latzin Philipp, Koerner-Rettberg Cordula

机构信息

Department of Pediatric Pneumology, University Children's Hospital Basel (UKBB), Basel, Switzerland Division of Respiratory Medicine, Department of Pediatrics, University Children's Hospital of Bern, Bern, Switzerland.

Department of Pediatric Pneumology, University Children's Hospital of Ruhr University Bochum at St Josef-Hospital, Bochum, Germany.

出版信息

Thorax. 2015 Sep;70(9):896. doi: 10.1136/thoraxjnl-2015-207206. Epub 2015 May 12.

DOI:10.1136/thoraxjnl-2015-207206
PMID:25967752
Abstract
摘要

相似文献

1
Further evidence for an association between LCI and FEV1 in patients with PCD.原发性纤毛运动障碍患者中LCI与第一秒用力呼气容积之间关联的进一步证据。
Thorax. 2015 Sep;70(9):896. doi: 10.1136/thoraxjnl-2015-207206. Epub 2015 May 12.
2
Lung structure-function correlation in patients with primary ciliary dyskinesia.原发性纤毛运动障碍患者的肺结构-功能相关性。
Thorax. 2015 Apr;70(4):339-45. doi: 10.1136/thoraxjnl-2014-206578. Epub 2015 Feb 11.
3
Lung clearance index predicts pulmonary exacerbations in individuals with primary ciliary dyskinesia: a multicentre cohort study.肺清除指数预测原发性纤毛运动障碍患者的肺部恶化:一项多中心队列研究。
Thorax. 2021 Jul;76(7):681-688. doi: 10.1136/thoraxjnl-2020-215504. Epub 2021 Jan 27.
4
Nitrogen washout measurements of lung clearance index (LCI).
Thorax. 2015 Sep;70(9):896-7. doi: 10.1136/thoraxjnl-2015-207309. Epub 2015 Jun 16.
5
Wavering in the breeze: is multiple breath washout useful in primary ciliary dyskinesia?在微风中摇曳:多次呼吸冲洗在原发性纤毛运动障碍中有用吗?
Thorax. 2015 Apr;70(4):305-6. doi: 10.1136/thoraxjnl-2015-206822. Epub 2015 Feb 13.
6
[Syndromes related to altered structures and function of the respiratory cilia].
Otolaryngol Pol. 1992;46(6):590-3.
7
Ciliary disorientation alone as a cause of primary ciliary dyskinesia syndrome.单独的睫状体定向障碍作为原发性睫状运动障碍综合征的一个病因
Am J Respir Crit Care Med. 1996 Mar;153(3):1123-9. doi: 10.1164/ajrccm.153.3.8630555.
8
Genetic defects in ciliary structure and function.纤毛结构和功能的基因缺陷。
Annu Rev Physiol. 2007;69:423-50. doi: 10.1146/annurev.physiol.69.040705.141301.
9
The clinical effect and the effect on the ciliary motility of oral N-acetylcysteine in patients with cystic fibrosis and primary ciliary dyskinesia.
Eur Respir J. 1988 Feb;1(2):161-7.
10
Nasal ciliary ultrastructure and function in patients with primary ciliary dyskinesia compared with that in normal subjects and in subjects with various respiratory diseases.原发性纤毛运动障碍患者的鼻纤毛超微结构和功能与正常受试者及各种呼吸系统疾病受试者的比较。
Am Rev Respir Dis. 1984 Jan;129(1):161-7. doi: 10.1164/arrd.1984.129.1.161.

引用本文的文献

1
Lung Function in Children with Primary Ciliary Dyskinesia.原发性纤毛运动障碍患儿的肺功能
Children (Basel). 2023 Feb 2;10(2):290. doi: 10.3390/children10020290.
2
Efficacy of hypertonic saline versus isotonic saline among children with cystic fibrosis: A systematic review and meta-analysis.高渗盐水与等渗盐水对囊性纤维化儿童的疗效:一项系统评价与荟萃分析。
Can J Respir Ther. 2023 Jan 20;59:1-7. doi: 10.29390/cjrt-2022-046. eCollection 2023.
3
Chronic airway disease in primary ciliary dyskinesia-spiced with geno-phenotype associations.
原发性纤毛运动障碍的慢性气道疾病——充满了基因表型关联。
Am J Med Genet C Semin Med Genet. 2022 Mar;190(1):20-35. doi: 10.1002/ajmg.c.31967. Epub 2022 Mar 29.
4
Lower airway clinical outcome measures for use in primary ciliary dyskinesia research: a scoping review.用于原发性纤毛运动障碍研究的下呼吸道临床结局指标:一项范围综述
ERJ Open Res. 2021 Nov 29;7(4). doi: 10.1183/23120541.00320-2021. eCollection 2021 Oct.
5
[Management of Primary Ciliary Dyskinesia].[原发性纤毛运动障碍的管理]
Pneumologie. 2020 Nov;74(11):750-765. doi: 10.1055/a-1235-1520. Epub 2020 Sep 25.
6
Comparison of Multiple Breath Washout and Spirometry in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis and Healthy Controls.原发性纤毛运动障碍和囊性纤维化患儿与健康对照者的多次呼吸冲洗和肺量测定比较。
Ann Am Thorac Soc. 2020 Sep;17(9):1085-1093. doi: 10.1513/AnnalsATS.201905-375OC.
7
Validation of pediatric health-related quality of life instruments for primary ciliary dyskinesia (QOL-PCD).验证用于原发性纤毛运动障碍(PCD)的儿科健康相关生活质量工具(QOL-PCD)。
Pediatr Pulmonol. 2019 Dec;54(12):2011-2020. doi: 10.1002/ppul.24507. Epub 2019 Sep 1.
8
Spirometric indices in primary ciliary dyskinesia: systematic review and meta-analysis.原发性纤毛运动障碍的肺量计指标:系统评价与荟萃分析
ERJ Open Res. 2019 May 10;5(2). doi: 10.1183/23120541.00231-2018. eCollection 2019 Apr.
9
One-year evolution and variability in multiple-breath washout indices in children and young adults with primary ciliary dyskinesia.原发性纤毛运动障碍儿童和青年多呼吸洗脱指数的一年演变及变异性
Eur Clin Respir J. 2019 Mar 26;6(1):1591841. doi: 10.1080/20018525.2019.1591841. eCollection 2019.
10
Comparison of different analysis algorithms to calculate multiple-breath washout outcomes.计算多次呼吸洗脱结果的不同分析算法的比较。
ERJ Open Res. 2018 Jul 13;4(3). doi: 10.1183/23120541.00021-2017. eCollection 2018 Jul.