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Items: 1 to 20 of 465

1.

Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis.

Gustafsson PM, De Jong PA, Tiddens HA, Lindblad A.

Thorax. 2008 Feb;63(2):129-34. Epub 2007 Aug 3.

PMID:
17675316
2.

Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis.

Aurora P, Gustafsson P, Bush A, Lindblad A, Oliver C, Wallis CE, Stocks J.

Thorax. 2004 Dec;59(12):1068-73.

3.

Tracking Lung Clearance Index and chest CT in mild cystic fibrosis lung disease over a period of three years.

Fuchs SI, Gappa M, Eder J, Unsinn KM, Steinkamp G, Ellemunter H.

Respir Med. 2014 Jun;108(6):865-74. doi: 10.1016/j.rmed.2014.03.011. Epub 2014 Mar 25.

4.

Comparison of Lung Clearance Index and Magnetic Resonance Imaging for Assessment of Lung Disease in Children with Cystic Fibrosis.

Stahl M, Wielpütz MO, Graeber SY, Joachim C, Sommerburg O, Kauczor HU, Puderbach M, Eichinger M, Mall MA.

Am J Respir Crit Care Med. 2017 Feb 1;195(3):349-359. doi: 10.1164/rccm.201604-0893OC.

PMID:
27575911
5.

Lung clearance index and high-resolution computed tomography scores in primary ciliary dyskinesia.

Irving SJ, Ives A, Davies G, Donovan J, Edey AJ, Gill SS, Nair A, Saunders C, Wijesekera NT, Alton EW, Hansell D, Hogg C, Davies JC, Bush A.

Am J Respir Crit Care Med. 2013 Sep 1;188(5):545-9. doi: 10.1164/rccm.201304-0800OC.

6.
7.

Pulmonary abnormalities on high-resolution CT demonstrate more rapid decline than FEV1 in adults with cystic fibrosis.

Judge EP, Dodd JD, Masterson JB, Gallagher CG.

Chest. 2006 Nov;130(5):1424-32.

PMID:
17099020
8.

Sensitivity of Lung Clearance Index and chest computed tomography in early CF lung disease.

Ellemunter H, Fuchs SI, Unsinn KM, Freund MC, Waltner-Romen M, Steinkamp G, Gappa M.

Respir Med. 2010 Dec;104(12):1834-42. doi: 10.1016/j.rmed.2010.06.010. Epub 2010 Jul 15.

9.

Lung structure-function correlation in patients with primary ciliary dyskinesia.

Boon M, Vermeulen FL, Gysemans W, Proesmans M, Jorissen M, De Boeck K.

Thorax. 2015 Apr;70(4):339-45. doi: 10.1136/thoraxjnl-2014-206578. Epub 2015 Feb 11.

PMID:
25673230
10.

Changes in structural lung disease in cystic fibrosis children over 4 years as evaluated by high-resolution computed tomography.

Carpio C, Albi G, Rayón-Aledo JC, Álvarez-Sala R, Girón R, Prados C, Caballero P.

Eur Radiol. 2015 Dec;25(12):3577-85. doi: 10.1007/s00330-015-3782-4. Epub 2015 May 1.

PMID:
25929944
11.

Improved air trapping evaluation in chest computed tomography in children with cystic fibrosis using real-time spirometric monitoring and biofeedback.

Kongstad T, Buchvald FF, Green K, Lindblad A, Robinson TE, Nielsen KG.

J Cyst Fibros. 2013 Dec;12(6):559-66. doi: 10.1016/j.jcf.2013.05.012. Epub 2013 Jun 27.

12.

Small airway involvement in cystic fibrosis lung disease: routine spirometry as an early and sensitive marker.

Bakker EM, Borsboom GJ, van der Wiel-Kooij EC, Caudri D, Rosenfeld M, Tiddens HA.

Pediatr Pulmonol. 2013 Nov;48(11):1081-8. doi: 10.1002/ppul.22777. Epub 2013 Feb 8.

PMID:
23401260
14.

Practicability of nitrogen multiple-breath washout measurements in a pediatric cystic fibrosis outpatient setting.

Singer F, Kieninger E, Abbas C, Yammine S, Fuchs O, Proietti E, Regamey N, Casaulta C, Frey U, Latzin P.

Pediatr Pulmonol. 2013 Aug;48(8):739-46. doi: 10.1002/ppul.22651. Epub 2012 Aug 8.

PMID:
22888105
15.

Multiple-breath washout as a marker of lung disease in preschool children with cystic fibrosis.

Aurora P, Bush A, Gustafsson P, Oliver C, Wallis C, Price J, Stroobant J, Carr S, Stocks J; London Cystic Fibrosis Collaboration.

Am J Respir Crit Care Med. 2005 Feb 1;171(3):249-56. Epub 2004 Oct 29.

PMID:
15516530
16.
17.

Retrospective review of children presenting with non cystic fibrosis bronchiectasis: HRCT features and clinical relationships.

Edwards EA, Metcalfe R, Milne DG, Thompson J, Byrnes CA.

Pediatr Pulmonol. 2003 Aug;36(2):87-93.

PMID:
12833486
18.

Lung clearance index at 4 years predicts subsequent lung function in children with cystic fibrosis.

Aurora P, Stanojevic S, Wade A, Oliver C, Kozlowska W, Lum S, Bush A, Price J, Carr SB, Shankar A, Stocks J; London Cystic Fibrosis Collaboration.

Am J Respir Crit Care Med. 2011 Mar 15;183(6):752-8. doi: 10.1164/rccm.200911-1646OC. Epub 2010 Oct 8.

PMID:
20935113
19.

Hyperpolarized 3helium magnetic resonance ventilation imaging of the lung in cystic fibrosis: comparison with high resolution CT and spirometry.

McMahon CJ, Dodd JD, Hill C, Woodhouse N, Wild JM, Fichele S, Gallagher CG, Skehan SJ, van Beek EJ, Masterson JB.

Eur Radiol. 2006 Nov;16(11):2483-90. Epub 2006 Jul 27.

PMID:
16871384
20.

Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis.

Horsley AR, Gustafsson PM, Macleod KA, Saunders C, Greening AP, Porteous DJ, Davies JC, Cunningham S, Alton EW, Innes JA.

Thorax. 2008 Feb;63(2):135-40. Epub 2007 Aug 3.

PMID:
17675315

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