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Items: 1 to 20 of 121

1.

Effect of macrolide on lung function and computed tomography (CT) score in non-cystic fibrosis bronchiectasis.

Goeminne PC, Soens J, Scheers H, De Wever W, Dupont L.

Acta Clin Belg. 2012 Sep-Oct;67(5):338-46.

PMID:
23189541
2.
3.

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.

PMID:
25929944
4.

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
5.

Structural and functional lung disease in primary ciliary dyskinesia.

Santamaria F, Montella S, Tiddens HA, Guidi G, Casotti V, Maglione M, de Jong PA.

Chest. 2008 Aug;134(2):351-7. doi: 10.1378/chest.07-2812.

PMID:
18403663
6.

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
7.

The use of high resolution computerized tomography (HRCT) of the chest in evaluating the effect of tobramycin solution for inhalation in cystic fibrosis lung disease.

Nasr SZ, Sakmar E, Christodoulou E, Eckhardt BP, Streetman DS, Strouse PJ.

Pediatr Pulmonol. 2010 May;45(5):440-9. doi: 10.1002/ppul.21188.

8.

Prolonged treatment with macrolides in adult patients with non-cystic fibrosis bronchiectasis: meta-analysis of randomized controlled trials.

Zhuo GY, He Q, Xiang-Lian L, Ya-Nan Y, Si-Te F.

Pulm Pharmacol Ther. 2014 Oct;29(1):80-8. doi: 10.1016/j.pupt.2014.02.002. Erratum in: Pulm Pharmacol Ther. 2014 Oct;29(1):90.

PMID:
24594263
9.

Spirometer-triggered high-resolution computed tomography and pulmonary function measurements during an acute exacerbation in patients with cystic fibrosis.

Robinson TE, Leung AN, Northway WH, Blankenberg FG, Bloch DA, Oehlert JW, Al-Dabbagh H, Hubli S, Moss RB.

J Pediatr. 2001 Apr;138(4):553-9.

PMID:
11295720
10.

Correlation of CT findings with clinical evaluations in 261 patients with symptomatic bronchiectasis.

Lynch DA, Newell J, Hale V, Dyer D, Corkery K, Fox NL, Gerend P, Fick R.

AJR Am J Roentgenol. 1999 Jul;173(1):53-8.

PMID:
10397099
11.

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.

PMID:
16871384
12.

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.

PMID:
17675316
13.

Automated CT scan scores of bronchiectasis and air trapping in cystic fibrosis.

DeBoer EM, Swiercz W, Heltshe SL, Anthony MM, Szefler P, Klein R, Strain J, Brody AS, Sagel SD.

Chest. 2014 Mar 1;145(3):593-603. doi: 10.1378/chest.13-0588.

14.
15.

Characterization of lung function impairment in adults with bronchiectasis.

Guan WJ, Gao YH, Xu G, Lin ZY, Tang Y, Li HM, Lin ZM, Zheng JP, Chen RC, Zhong NS.

PLoS One. 2014 Nov 18;9(11):e113373. doi: 10.1371/journal.pone.0113373.

16.
17.

Mortality in non-cystic fibrosis bronchiectasis: a prospective cohort analysis.

Goeminne PC, Nawrot TS, Ruttens D, Seys S, Dupont LJ.

Respir Med. 2014 Feb;108(2):287-96. doi: 10.1016/j.rmed.2013.12.015.

18.
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[Effect of rhDNase on the respiratory function and nutritional status of children and adolescents with mucoviscidosis].

Wizla-Derambure N, Michaud L, Sardet A, Deschildre A, Loeuille GA, Tassin E, Loire N, Buisine C, Boutry E, Dias J, Hecquet F, Turck D.

Arch Pediatr. 1998 Apr;5(4):378-83. French.

PMID:
9759156
20.

Correlation between Bhalla score and spirometry in children and adolescents with cystic fibrosis.

Pereira FF, Ibiapina Cda C, Alvim CG, Camargos PA, Figueiredo R, Pedrosa JF.

Rev Assoc Med Bras (1992). 2014 May-Jun;60(3):216-21.

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