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Journal Abstract Search
1210 related items for PubMed ID: 17675316
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. PubMed ID: 17675316 [Abstract] [Full Text] [Related]
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. PubMed ID: 15563707 [Abstract] [Full Text] [Related]
3. Comparison of Multiple Breath Washout and Spirometry in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis and Healthy Controls. Kinghorn B, McNamara S, Genatossio A, Sullivan E, Siegel M, Bauer I, Clem C, Johnson RC, Davis M, Griffiths A, Wheeler W, Johnson K, Davis SD, Leigh MW, Rosenfeld M, Pittman J. Ann Am Thorac Soc; 2020 Sep; 17(9):1085-1093. PubMed ID: 32603187 [Abstract] [Full Text] [Related]
8. Single-breath washout and association with structural lung disease in children with cystic fibrosis. Yammine S, Ramsey KA, Skoric B, King L, Latzin P, Rosenow T, Hall GL, Ranganathan SC, AREST CF. Pediatr Pulmonol; 2019 May; 54(5):587-594. PubMed ID: 30758143 [Abstract] [Full Text] [Related]
9. Abnormal Lung Clearance Index in Cystic Fibrosis Children with Normal FEV1 and Single-Breath Nitrogen Washout Test. Kasi AS, Wee CP, Keens TG, Salinas DB. Lung; 2021 Feb; 199(1):37-41. PubMed ID: 33389068 [Abstract] [Full Text] [Related]
10. Comparative sensitivity of early cystic fibrosis lung disease detection tools in school aged children. Bayfield KJ, Weinheimer O, Middleton A, Boyton C, Fitzpatrick R, Kennedy B, Blaxland A, Jayasuriya G, Caplain N, Wielpütz MO, Yu L, Galban CJ, Robinson TE, Bartholmai B, Gustafsson P, Fitzgerald D, Selvadurai H, Robinson PD. J Cyst Fibros; 2024 Sep; 23(5):918-925. PubMed ID: 38969602 [Abstract] [Full Text] [Related]
11. 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. PubMed ID: 24726097 [Abstract] [Full Text] [Related]
12. 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]
13. 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 01; 188(5):545-9. PubMed ID: 23815669 [Abstract] [Full Text] [Related]
14. 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 01; 12(6):559-66. PubMed ID: 23810566 [Abstract] [Full Text] [Related]
15. 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 01; 48(11):1081-8. PubMed ID: 23401260 [Abstract] [Full Text] [Related]
16. Air trapping on expiratory high-resolution CT scans in the absence of inspiratory scan abnormalities: correlation with pulmonary function tests and differential diagnosis. Arakawa H, Webb WR. AJR Am J Roentgenol; 1998 May 01; 170(5):1349-53. PubMed ID: 9574614 [Abstract] [Full Text] [Related]
17. 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 01; 48(8):739-46. PubMed ID: 22888105 [Abstract] [Full Text] [Related]
18. 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 01; 171(3):249-56. PubMed ID: 15516530 [Abstract] [Full Text] [Related]
19. High-resolution computed tomography in young patients with cystic fibrosis: distribution of abnormalities and correlation with pulmonary function tests. Brody AS, Klein JS, Molina PL, Quan J, Bean JA, Wilmott RW. J Pediatr; 2004 Jul 01; 145(1):32-8. PubMed ID: 15238903 [Abstract] [Full Text] [Related]
20. 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 01; 25(12):3577-85. PubMed ID: 25929944 [Abstract] [Full Text] [Related] Page: [Next] [New Search]