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139 related items for PubMed ID: 16182669
1. Sex differences in habitual physical activity and lung function decline in children with cystic fibrosis. Schneiderman-Walker J, Wilkes DL, Strug L, Lands LC, Pollock SL, Selvadurai HC, Hay J, Coates AL, Corey M. J Pediatr; 2005 Sep; 147(3):321-6. PubMed ID: 16182669 [Abstract] [Full Text] [Related]
2. Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patient Registry. Zemel BS, Jawad AF, FitzSimmons S, Stallings VA. J Pediatr; 2000 Sep; 137(3):374-80. PubMed ID: 10969263 [Abstract] [Full Text] [Related]
3. Reliability and validity of the habitual activity estimation scale (HAES) in patients with cystic fibrosis. Wells GD, Wilkes DL, Schneiderman-Walker J, Elmi M, Tullis E, Lands LC, Ratjen F, Coates AL. Pediatr Pulmonol; 2008 Apr; 43(4):345-53. PubMed ID: 18306334 [Abstract] [Full Text] [Related]
4. Relationship between FEV1 and peak oxygen uptake in children with cystic fibrosis. Pianosi P, LeBlanc J, Almudevar A. Pediatr Pulmonol; 2005 Oct; 40(4):324-9. PubMed ID: 16082708 [Abstract] [Full Text] [Related]
5. Longitudinal relationship between physical activity and lung health in patients with cystic fibrosis. Schneiderman JE, Wilkes DL, Atenafu EG, Nguyen T, Wells GD, Alarie N, Tullis E, Lands LC, Coates AL, Corey M, Ratjen F. Eur Respir J; 2014 Mar; 43(3):817-23. PubMed ID: 24176992 [Abstract] [Full Text] [Related]
6. A randomized controlled trial of a 3-year home exercise program in cystic fibrosis. Schneiderman-Walker J, Pollock SL, Corey M, Wilkes DD, Canny GJ, Pedder L, Reisman JJ. J Pediatr; 2000 Mar; 136(3):304-10. PubMed ID: 10700685 [Abstract] [Full Text] [Related]
7. Does carbon dioxide retention during exercise predict a more rapid decline in FEV1 in cystic fibrosis? Javadpour SM, Selvadurai H, Wilkes DL, Schneiderman-Walker J, Coates AL. Arch Dis Child; 2005 Aug; 90(8):792-5. PubMed ID: 16040875 [Abstract] [Full Text] [Related]
8. Gender differences in habitual activity in children with cystic fibrosis. Selvadurai HC, Blimkie CJ, Cooper PJ, Mellis CM, Van Asperen PP. Arch Dis Child; 2004 Oct; 89(10):928-33. PubMed ID: 15383436 [Abstract] [Full Text] [Related]
9. Improving rate of decline of FEV1 in young adults with cystic fibrosis. Que C, Cullinan P, Geddes D. Thorax; 2006 Feb; 61(2):155-7. PubMed ID: 16384880 [Abstract] [Full Text] [Related]
10. Exercise and physical activity in children with cystic fibrosis. Wilkes DL, Schneiderman JE, Nguyen T, Heale L, Moola F, Ratjen F, Coates AL, Wells GD. Paediatr Respir Rev; 2009 Sep; 10(3):105-9. PubMed ID: 19651380 [Abstract] [Full Text] [Related]
11. Measuring habitual physical activity in adults with cystic fibrosis. Savi D, Quattrucci S, Internullo M, De Biase RV, Calverley PM, Palange P. Respir Med; 2013 Dec; 107(12):1888-94. PubMed ID: 24094944 [Abstract] [Full Text] [Related]
12. Peak oxygen uptake and mortality in children with cystic fibrosis. Pianosi P, Leblanc J, Almudevar A. Thorax; 2005 Jan; 60(1):50-4. PubMed ID: 15618583 [Abstract] [Full Text] [Related]
13. Preserved diffusion capacity in children with cystic fibrosis. Merkus PJ, Govaere ES, Hop WH, Stam H, Tiddens HA, de Jongste JC. Pediatr Pulmonol; 2004 Jan; 37(1):56-60. PubMed ID: 14679490 [Abstract] [Full Text] [Related]
14. Longitudinal analysis of FEV1 changes related to antibiotic therapy in children with cystic fibrosis. Javadpour S, Jones A, Brownlee K. Ir Med J; 2007 Jan; 100(7):529-32. PubMed ID: 17886526 [Abstract] [Full Text] [Related]
15. Growth and lung function in Asian patients with cystic fibrosis. Callaghan BD, Hoo AF, Dinwiddie R, Balfour-Lynn IM, Carr SB. Arch Dis Child; 2005 Oct; 90(10):1029-32. PubMed ID: 16177157 [Abstract] [Full Text] [Related]
16. Gender differences in treatment adherence among youth with cystic fibrosis: development of a new questionnaire. Patterson JM, Wall M, Berge J, Milla C. J Cyst Fibros; 2008 Mar; 7(2):154-64. PubMed ID: 17719857 [Abstract] [Full Text] [Related]
17. Exercise improves lung function and habitual activity in children with cystic fibrosis. Paranjape SM, Barnes LA, Carson KA, von Berg K, Loosen H, Mogayzel PJ. J Cyst Fibros; 2012 Jan; 11(1):18-23. PubMed ID: 21890433 [Abstract] [Full Text] [Related]
18. Infant care patterns at epidemiologic study of cystic fibrosis sites that achieve superior childhood lung function. Padman R, McColley SA, Miller DP, Konstan MW, Morgan WJ, Schechter MS, Ren CL, Wagener JS, Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Pediatrics; 2007 Mar; 119(3):e531-7. PubMed ID: 17332172 [Abstract] [Full Text] [Related]
19. Breathing pattern adopted by children with cystic fibrosis with mild to moderate pulmonary impairment during exercise. Keochkerian D, Chlif M, Delanaud S, Gauthier R, Maingourd Y, Ahmaidi S. Respiration; 2008 Mar; 75(2):170-7. PubMed ID: 17148933 [Abstract] [Full Text] [Related]
20. Realities of expectorated sputum collection in the pediatric cystic fibrosis clinic. Radhakrishnan DK, Corey M, Dell SD. Arch Pediatr Adolesc Med; 2007 Jun; 161(6):603-6. PubMed ID: 17548767 [Abstract] [Full Text] [Related] Page: [Next] [New Search]