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Results: 1 to 20 of 73

Similar articles for PubMed (Select 22172941)

1.

Patient indicators of a pulmonary exacerbation: preliminary reports from school aged children map onto those of adults.

Abbott J, Holt A, Morton AM, Hart A, Milne G, Wolfe SP, Conway SP.

J Cyst Fibros. 2012 May;11(3):180-6. doi: 10.1016/j.jcf.2011.11.005. Epub 2011 Dec 14.

2.

Indicators of pulmonary exacerbation in cystic fibrosis: A Delphi survey of patients and health professionals.

McCourt F, O'Neill B, Logan I, Abbott J, Plant B, McCrum-Gardner E, McKeown S, Stuart Elborn J, Bradley JM.

J Cyst Fibros. 2015 Jan;14(1):90-6. doi: 10.1016/j.jcf.2014.06.007. Epub 2014 Aug 12.

PMID:
25127921
3.

Factors associated with a shorter time until the next pulmonary exacerbation in adult patients with cystic fibrosis.

Sequeiros IM, Jarad N.

Chron Respir Dis. 2012 Feb;9(1):9-16. doi: 10.1177/1479972311433575.

PMID:
22308550
4.

The natural history of acute upper respiratory tract infections in children.

Mitra A, Hannay D, Kapur A, Baxter G.

Prim Health Care Res Dev. 2011 Oct;12(4):329-34. doi: 10.1017/S1463423611000193.

PMID:
22284947
5.

Determining presence of lung disease in young children with cystic fibrosis: lung clearance index, oxygen saturation and cough frequency.

Bakker EM, van der Meijden JC, Nieuwhof EM, Hop WC, Tiddens HA.

J Cyst Fibros. 2012 May;11(3):223-30. doi: 10.1016/j.jcf.2011.12.003. Epub 2012 Jan 23.

6.

Chronic Stenotrophomonas maltophilia infection and exacerbation outcomes in cystic fibrosis.

Waters V, Atenafu EG, Salazar JG, Lu A, Yau Y, Matukas L, Tullis E, Ratjen F.

J Cyst Fibros. 2012 Jan;11(1):8-13. doi: 10.1016/j.jcf.2011.07.008. Epub 2011 Aug 16.

7.

Defining pulmonary exacerbation in children with non-cystic fibrosis bronchiectasis.

Kapur N, Masters IB, Morris PS, Galligan J, Ware R, Chang AB.

Pediatr Pulmonol. 2012 Jan;47(1):68-75. doi: 10.1002/ppul.21518. Epub 2011 Aug 9.

PMID:
21830316
8.

Exacerbation frequency and clinical outcomes in adult patients with cystic fibrosis.

de Boer K, Vandemheen KL, Tullis E, Doucette S, Fergusson D, Freitag A, Paterson N, Jackson M, Lougheed MD, Kumar V, Aaron SD.

Thorax. 2011 Aug;66(8):680-5. doi: 10.1136/thx.2011.161117. Epub 2011 Jun 15.

PMID:
21680566
9.

Approach to treating cystic fibrosis pulmonary exacerbations varies widely across US CF care centers.

Kraynack NC, Gothard MD, Falletta LM, McBride JT.

Pediatr Pulmonol. 2011 Sep;46(9):870-81. doi: 10.1002/ppul.21442. Epub 2011 Apr 4.

PMID:
21465675
10.

Pulmonary exacerbations are associated with subsequent FEV1 decline in both adults and children with cystic fibrosis.

Sanders DB, Bittner RC, Rosenfeld M, Redding GJ, Goss CH.

Pediatr Pulmonol. 2011 Apr;46(4):393-400. doi: 10.1002/ppul.21374. Epub 2010 Oct 21.

PMID:
20967845
11.

Longitudinal growth and lung function in pediatric non-cystic fibrosis bronchiectasis: what influences lung function stability?

Kapur N, Masters IB, Chang AB.

Chest. 2010 Jul;138(1):158-64. doi: 10.1378/chest.09-2932. Epub 2010 Feb 19.

PMID:
20173055
12.

Frequency and self-management of pain, dyspnea, and cough in cystic fibrosis.

Stenekes SJ, Hughes A, Grégoire MC, Frager G, Robinson WM, McGrath PJ.

J Pain Symptom Manage. 2009 Dec;38(6):837-48. doi: 10.1016/j.jpainsymman.2009.04.029. Epub .

PMID:
19819666
13.

What defines a pulmonary exacerbation? The perceptions of adults with cystic fibrosis.

Abbott J, Holt A, Hart A, Morton AM, MacDougall L, Pogson M, Milne G, Rodgers HC, Conway SP.

J Cyst Fibros. 2009 Sep;8(5):356-9. doi: 10.1016/j.jcf.2009.07.003. Epub 2009 Aug 8.

14.

Using index of ventilation to assess response to treatment for acute pulmonary exacerbation in children with cystic fibrosis.

Robinson PD, Cooper P, Van Asperen P, Fitzgerald D, Selvadurai H.

Pediatr Pulmonol. 2009 Aug;44(8):733-42. doi: 10.1002/ppul.20956.

PMID:
19598271
15.

Patient-reported respiratory symptoms in cystic fibrosis.

Goss CH, Edwards TC, Ramsey BW, Aitken ML, Patrick DL.

J Cyst Fibros. 2009 Jul;8(4):245-52. doi: 10.1016/j.jcf.2009.04.003. Epub 2009 May 29.

16.

Health related quality of life in cystic fibrosis: To work or not to work?

Havermans T, Colpaert K, Vanharen L, Dupont LJ.

J Cyst Fibros. 2009 May;8(3):218-23. doi: 10.1016/j.jcf.2009.03.002. Epub 2009 Mar 28.

17.

Lung clearance index in the assessment of airways disease.

Horsley A.

Respir Med. 2009 Jun;103(6):793-9. doi: 10.1016/j.rmed.2009.01.025. Epub 2009 Feb 25. Review.

18.

Reproducibility of spirometry during cystic fibrosis pulmonary exacerbations.

Sanders DB, Rosenfeld M, Mayer-Hamblett N, Stamey D, Redding GJ.

Pediatr Pulmonol. 2008 Nov;43(11):1142-6. doi: 10.1002/ppul.20924.

PMID:
18846562
19.

A new scoring system in Cystic Fibrosis: statistical tools for database analysis - a preliminary report.

Hafen GM, Hurst C, Yearwood J, Smith J, Dzalilov Z, Robinson PJ.

BMC Med Inform Decis Mak. 2008 Oct 5;8:44. doi: 10.1186/1472-6947-8-44.

20.

Non-invasive tension time index in relation to severity of disease in children with cystic fibrosis.

Hahn A, Ankermann T, Claass A, Mann M, Lindemann H, Neubauer BA.

Pediatr Pulmonol. 2008 Oct;43(10):973-81. doi: 10.1002/ppul.20887.

PMID:
18780334
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