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112 related items for PubMed ID: 2405342
1. Variability of pulmonary function tests in cystic fibrosis. Cooper PJ, Robertson CF, Hudson IL, Phelan PD. Pediatr Pulmonol; 1990; 8(1):16-22. PubMed ID: 2405342 [Abstract] [Full Text] [Related]
3. The six-minute walking test in children with cystic fibrosis: reliability and validity. Gulmans VA, van Veldhoven NH, de Meer K, Helders PJ. Pediatr Pulmonol; 1996 Aug; 22(2):85-9. PubMed ID: 8875580 [Abstract] [Full Text] [Related]
5. Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis. Gustafsson PM, Aurora P, Lindblad A. Eur Respir J; 2003 Dec; 22(6):972-9. PubMed ID: 14680088 [Abstract] [Full Text] [Related]
6. Respiratory muscle function in patients with cystic fibrosis. Dassios T, Katelari A, Doudounakis S, Mantagos S, Dimitriou G. Pediatr Pulmonol; 2013 Sep; 48(9):865-73. PubMed ID: 23143864 [Abstract] [Full Text] [Related]
8. Lung function abnormalities in cystic fibrosis and changes during growth. Zapletal A, Houstek J, Samanek M, Vavrova V, Srajer J. Bull Eur Physiopathol Respir; 1979 Sep; 15(4):575-92. PubMed ID: 497487 [Abstract] [Full Text] [Related]
12. Within-subject variability and per cent change for significance of spirometry in normal subjects and in patients with cystic fibrosis. Nickerson BG, Lemen RJ, Gerdes CB, Wegmann MJ, Robertson G. Am Rev Respir Dis; 1980 Dec; 122(6):859-66. PubMed ID: 7458059 [Abstract] [Full Text] [Related]
15. Is an FEV1 of 80% predicted a normal spirometry in cystic fibrosis children and adults? König P, Ner Z, Acton JD, Ge B, Hewett J. Clin Respir J; 2018 Aug; 12(8):2397-2403. PubMed ID: 29920961 [Abstract] [Full Text] [Related]
16. 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. PubMed ID: 17675316 [Abstract] [Full Text] [Related]
18. Analysis of a large cohort of cystic fibrosis patients with severe liver disease indicates lung function decline does not significantly differ from that of the general cystic fibrosis population. Polineni D, Piccorelli AV, Hannah WB, Dalrymple SN, Pace RG, Durie PR, Ling SC, Knowles MR, Stonebraker JR. PLoS One; 2018 Feb; 13(10):e0205257. PubMed ID: 30307979 [Abstract] [Full Text] [Related]