Suppr超能文献

Update in cystic fibrosis 2012.

作者信息

Goss Christopher H, Ratjen Felix

机构信息

Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of Washington, Seattle, WA, USA.

出版信息

Am J Respir Crit Care Med. 2013 May 1;187(9):915-9. doi: 10.1164/rccm.201301-0184UP.

Abstract
摘要

相似文献

1
Update in cystic fibrosis 2012.
Am J Respir Crit Care Med. 2013 May 1;187(9):915-9. doi: 10.1164/rccm.201301-0184UP.
2
Hypertonic saline for cystic fibrosis: worth its salt?
Expert Rev Respir Med. 2014 Jun;8(3):267-9. doi: 10.1586/17476348.2014.896203. Epub 2014 Mar 26.
3
Inhaled hypertonic saline as a therapy for cystic fibrosis.
Curr Opin Pulm Med. 2006 Nov;12(6):445-52. doi: 10.1097/01.mcp.0000245714.89632.b2.
4
Hypertonic saline in cystic fibrosis.
Pediatr Pulmonol. 1996 Feb;21(2):73-4. doi: 10.1002/(SICI)1099-0496(199602)21:2<73::AID-PPUL1>3.0.CO;2-Q.
5
Mechanisms and applications of hypertonic saline.
J R Soc Med. 2011 Jul;104 Suppl 1(Suppl 1):S2-5. doi: 10.1258/jrsm.2011.s11101.
7
What did we learn from the North American Cystic Fibrosis Conference?
J R Soc Med. 2008 Jul;101 Suppl 1(Suppl 1):S6-9. doi: 10.1258/jrsm.2008.s18003.
9
Effect of hypertonic saline, amiloride, and cough on mucociliary clearance in patients with cystic fibrosis.
Am J Respir Crit Care Med. 1996 May;153(5):1503-9. doi: 10.1164/ajrccm.153.5.8630593.
10
Timing of hypertonic saline inhalation for cystic fibrosis.
Cochrane Database Syst Rev. 2012 Feb 15(2):CD008816. doi: 10.1002/14651858.CD008816.pub2.

引用本文的文献

1
Not Quite the Bully in the Schoolyard: Can Survive and Coexist with in the Cystic Fibrosis Lung.
Am J Respir Crit Care Med. 2021 Feb 1;203(3):279-281. doi: 10.1164/rccm.202008-3077ED.
2
CNS imaging studies in cystic fibrosis patients presenting with sudden neurological events.
BMJ Open Respir Res. 2019 Aug 9;6(1):e000456. doi: 10.1136/bmjresp-2019-000456. eCollection 2019.
3
Stem cell-derived organoids to model gastrointestinal facets of cystic fibrosis.
United European Gastroenterol J. 2017 Aug;5(5):609-624. doi: 10.1177/2050640616670565. Epub 2016 Sep 21.
5
Analysis and Characterization of Staphylococcus aureus Small Colony Variants Isolated From Cystic Fibrosis Patients in Austria.
Curr Microbiol. 2016 May;72(5):606-11. doi: 10.1007/s00284-016-0994-z. Epub 2016 Jan 28.
6
Cost-of-illness analysis and regression modeling in cystic fibrosis: a retrospective prevalence-based study.
Eur J Health Econ. 2017 Jan;18(1):73-82. doi: 10.1007/s10198-015-0759-9. Epub 2016 Jan 7.
8
Evidence for a Cystic Fibrosis Enteropathy.
PLoS One. 2015 Oct 20;10(10):e0138062. doi: 10.1371/journal.pone.0138062. eCollection 2015.
10
The Evolution of Cystic Fibrosis Care.
Chest. 2015 Aug;148(2):533-542. doi: 10.1378/chest.14-1997.

本文引用的文献

1
Socioeconomic barriers to lung transplantation: balancing access and equity.
Am J Respir Crit Care Med. 2012 Nov 15;186(10):937-9. doi: 10.1164/rccm.201210-1776ED.
2
Induced sputum biomarkers for monitoring cystic fibrosis lung disease.
Am J Respir Crit Care Med. 2012 Nov 1;186(9):812-4. doi: 10.1164/rccm.201209-1731ED.
3
Disparities in access to lung transplantation for patients with cystic fibrosis by socioeconomic status.
Am J Respir Crit Care Med. 2012 Nov 15;186(10):1008-13. doi: 10.1164/rccm.201205-0949OC. Epub 2012 Sep 13.
4
Assessment of F/HN-pseudotyped lentivirus as a clinically relevant vector for lung gene therapy.
Am J Respir Crit Care Med. 2012 Nov 1;186(9):846-56. doi: 10.1164/rccm.201206-1056OC. Epub 2012 Sep 6.
6
The effect of Aspergillus fumigatus infection on vitamin D receptor expression in cystic fibrosis.
Am J Respir Crit Care Med. 2012 Nov 15;186(10):999-1007. doi: 10.1164/rccm.201203-0478OC. Epub 2012 Aug 16.
7
Sputum biomarkers of inflammation and lung function decline in children with cystic fibrosis.
Am J Respir Crit Care Med. 2012 Nov 1;186(9):857-65. doi: 10.1164/rccm.201203-0507OC. Epub 2012 Aug 16.
8
Direct sampling of cystic fibrosis lungs indicates that DNA-based analyses of upper-airway specimens can misrepresent lung microbiota.
Proc Natl Acad Sci U S A. 2012 Aug 21;109(34):13769-74. doi: 10.1073/pnas.1107435109. Epub 2012 Aug 7.
9
Phenazine content in the cystic fibrosis respiratory tract negatively correlates with lung function and microbial complexity.
Am J Respir Cell Mol Biol. 2012 Dec;47(6):738-45. doi: 10.1165/rcmb.2012-0088OC. Epub 2012 Aug 3.
10
β-adrenergic sweat secretion as a diagnostic test for cystic fibrosis.
Am J Respir Crit Care Med. 2012 Oct 15;186(8):732-9. doi: 10.1164/rccm.201205-0922OC. Epub 2012 Aug 2.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验