• 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

The diagnosis of cystic fibrosis.

作者信息

Stern R C

机构信息

LeRoy W. Matthews Cystic Fibrosis Center, the Department of Pediatrics, Case Western Reserve University, OH, USA.

出版信息

N Engl J Med. 1997 Feb 13;336(7):487-91. doi: 10.1056/NEJM199702133360707.

DOI:10.1056/NEJM199702133360707
PMID:9017943
Abstract
摘要

相似文献

1
The diagnosis of cystic fibrosis.囊性纤维化的诊断。
N Engl J Med. 1997 Feb 13;336(7):487-91. doi: 10.1056/NEJM199702133360707.
2
Congenital bilateral absence of vas deferens in absence of cystic fibrosis.先天性双侧输精管缺如且无囊性纤维化。
Lancet. 1995 Jan 21;345(8943):200-1.
3
Diagnostic criteria for cystic fibrosis in men with congenital absence of the vas deferens.
Medicine (Baltimore). 1995 Jan;74(1):42-7. doi: 10.1097/00005792-199501000-00004.
4
Congenital absence of vas deferens and cystic fibrosis.先天性输精管缺如与囊性纤维化。
Minerva Pediatr. 2003 Feb;55(1):43-7, 47-50.
5
Cystic fibrosis presenting with haematological abnormalities.表现为血液学异常的囊性纤维化。
Clin Lab Haematol. 2006 Dec;28(6):423-6. doi: 10.1111/j.1365-2257.2006.00822.x.
6
Mutations in CFTR gene and clinical correlation in Argentine patients with congenital bilateral absence of the vas deferens.阿根廷先天性双侧输精管缺如患者CFTR基因的突变及临床相关性
Medicina (B Aires). 2004;64(3):213-8.
7
[A study evaluating the correlation between the phenotype and genotype among 65 cystic fibrosis patients].一项评估65例囊性纤维化患者表型与基因型之间相关性的研究
Pediatr Pol. 1995 Aug;70(8):633-8.
8
Sweat electrolyte and cystic fibrosis mutation analysis allows early diagnosis in Brazilian children with clinical signs compatible with cystic fibrosis.
Am J Med Genet. 1998 Apr 1;76(4):288-90.
9
Normal sweat chloride values do not exclude the diagnosis of cystic fibrosis.正常的汗液氯化物值不能排除囊性纤维化的诊断。
Am J Respir Crit Care Med. 1995 Nov;152(5 Pt 1):1736-7. doi: 10.1164/ajrccm.152.5.7582320.
10
Molecular screening of CFTR gene in Brazilian men with bilateral agenesis of the vas deferens.对巴西双侧输精管缺如男性进行囊性纤维化跨膜传导调节因子（CFTR）基因的分子筛查。
Hum Fertil (Camb). 2006 Mar;9(1):53-6. doi: 10.1080/14647270500440598.

引用本文的文献

1
Physical activity and its correlates in people with cystic fibrosis: a systematic review.囊性纤维化患者的身体活动及其相关因素：一项系统综述。
Eur Respir Rev. 2022 Sep 7;31(165). doi: 10.1183/16000617.0010-2022. Print 2022 Sep 30.
2
Occurrence of COVID-19 in cystic fibrosis patients: a review.囊性纤维化患者中新型冠状病毒肺炎的发生情况：一项综述
Front Microbiol. 2024 Apr 17;15:1356926. doi: 10.3389/fmicb.2024.1356926. eCollection 2024.
3
Current Trends in the Development of Electrochemical Biosensor for Detecting Analytes from Sweat.
电化学生物传感器检测汗液中分析物的最新研究进展
Curr Med Chem. 2024;31(25):3882-3898. doi: 10.2174/0929867331666230807143639.
4
Corneal opacification, an atypical presentation of cystic fibrosis: a case report and review of the literature.角膜混浊，囊性纤维化的一种非典型表现：病例报告及文献复习。
J Med Case Rep. 2022 May 12;16(1):188. doi: 10.1186/s13256-022-03410-x.
5
Flexible potentiometric pH sensors for wearable systems.用于可穿戴系统的柔性电位pH传感器。
RSC Adv. 2020 Feb 27;10(15):8594-8617. doi: 10.1039/d0ra00016g.
6
Serratus Anterior Plane Block as a Primary Anesthetic Technique for Video-Assisted Thoracic Surgery in a Child.前锯肌平面阻滞作为儿童电视辅助胸腔镜手术的主要麻醉技术
Cureus. 2021 May 27;13(5):e15283. doi: 10.7759/cureus.15283.
7
Physiological study of pulmonary involvement in adults with cystic fibrosis through simulated modeling of different clinical scenarios.通过模拟不同临床场景，对成人囊性纤维化肺部受累进行生理学研究。
Med Biol Eng Comput. 2019 Feb;57(2):413-425. doi: 10.1007/s11517-018-1885-1. Epub 2018 Sep 1.
8
Metabolomic Analysis by Nuclear Magnetic Resonance Spectroscopy as a New Approach to Understanding Inflammation and Monitoring of Pharmacological Therapy in Children and Young Adults With Cystic Fibrosis.通过核磁共振波谱进行代谢组学分析作为理解炎症和监测囊性纤维化儿童及青年药理治疗的新方法
Front Pharmacol. 2018 Jun 18;9:595. doi: 10.3389/fphar.2018.00595. eCollection 2018.
9
Screening for cystic fibrosis in New York State: considerations for algorithm improvements.纽约州囊性纤维化的筛查：算法改进的考量因素
Eur J Pediatr. 2016 Feb;175(2):181-93. doi: 10.1007/s00431-015-2616-3. Epub 2015 Aug 21.
10
Distribution of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mutations in a Cohort of Patients Residing in Palestine.居住在巴勒斯坦的一组患者中囊性纤维化跨膜传导调节因子（CFTR）突变的分布情况。
PLoS One. 2015 Jul 24;10(7):e0133890. doi: 10.1371/journal.pone.0133890. eCollection 2015.