-
1
-
-
33846229616
-
Priorities for respiratory research in the UK
-
DOI 10.1136/thx.2006.073882
-
Holgate ST. Priorities for respiratory research in the UK. Thorax 2007;62:5-7. (Pubitemid 46101759)
-
(2007)
Thorax
, vol.62
, Issue.1
, pp. 5-7
-
-
Holgate, S.T.1
-
2
-
-
66849138757
-
Monitoring respiratory disease severity in cystic fibrosis
-
Davies JC, Alton EW. Monitoring respiratory disease severity in cystic fibrosis. Respir Care 2009;54 :606-17.
-
(2009)
Respir Care
, vol.54
, pp. 606-617
-
-
Davies, J.C.1
Alton, E.W.2
-
3
-
-
34548660457
-
Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary
-
DOI 10.1164/rccm.200703-456SO
-
Rabe KF, Hurd S, Anzueto A, et al Global Initiative for Chronic Obstructive Lung Disease. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Am J Respir Crit Care Med 2007;176:532-55. (Pubitemid 47403272)
-
(2007)
American Journal of Respiratory and Critical Care Medicine
, vol.176
, Issue.6
, pp. 532-555
-
-
Rabe, K.F.1
Hurd, S.2
Anzueto, A.3
Barnes, P.J.4
Buist, S.A.5
Calverley, P.6
Fukuchi, Y.7
Jenkins, C.8
Rodriguez-Roisin, R.9
Van Weel, C.10
Zielinski, J.11
-
4
-
-
34447530328
-
Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis
-
Konstan MW, Morgan WJ, Butler SM, et al. Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis. J Pediatr 2007;151:134 e9, 139.e1.
-
(2007)
J Pediatr
, vol.151
-
-
Konstan, M.W.1
Morgan, W.J.2
Butler, S.M.3
-
5
-
-
36848999782
-
1 decline in children with cystic fibrosis
-
DOI 10.1164/rccm.200702-181OC
-
Konstan MW, Schluchter MD, Xue W, et al. Clinical use of ibuprofen is associated with slower FEV1 decline in children with cystic fibrosis. Am J Respir Crit Care Med 2007;176:1084-9. (Pubitemid 350223754)
-
(2007)
American Journal of Respiratory and Critical Care Medicine
, vol.176
, Issue.11
, pp. 1084-1089
-
-
Konstan, M.W.1
Schluchter, M.D.2
Xue, W.3
Davis, P.B.4
-
6
-
-
0027287651
-
Efficacy of aerosolized tobramycin in patients with cystic fibrosis
-
DOI 10.1056/NEJM199306173282403
-
Ramsey BW, Dorkin HL, Eisenberg JD, et al. Efficacy of aerosolized tobramycin in patients with cystic fibrosis. N Engl J Med 1993;328:1740-6. (Pubitemid 23170123)
-
(1993)
New England Journal of Medicine
, vol.328
, Issue.24
, pp. 1740-1746
-
-
Ramsey, B.W.1
Dorkin, H.L.2
Eisenberg, J.D.3
Gibson, R.L.4
Harwood, I.R.5
Kravitz, R.M.6
Schidlow, D.V.7
Wilmott, R.W.8
Astley, S.J.9
McBurnie, M.A.10
Wentz, K.11
Smith, A.L.12
-
7
-
-
0026520359
-
Prediction of mortality in patients with cystic fibrosis
-
Kerem E, Reisman J, Corey M, et al. Prediction of mortality in patients with cystic fibrosis. N Engl J Med 1992;326:1187-91.
-
(1992)
N Engl J Med
, vol.326
, pp. 1187-1191
-
-
Kerem, E.1
Reisman, J.2
Corey, M.3
-
8
-
-
79952522208
-
Improved survival at low lung function in cystic fibrosis: Cohort study from 1990 to 2007
-
George PM, Banya W, Pareek N, et al. Improved survival at low lung function in cystic fibrosis: cohort study from 1990 to 2007. BMJ 2011; 342:d1008.
-
(2011)
BMJ
, vol.342
-
-
George, P.M.1
Banya, W.2
Pareek, N.3
-
9
-
-
34548278908
-
Power considerations for studies of lung function in cystic fibrosis
-
DOI 10.1513/pats.200611-176HT
-
Corey M. Power considerations for studies of lung function in cystic fibrosis. Proc Am Thorac Soc 2007; 4:334-7. (Pubitemid 47330866)
-
(2007)
Proceedings of the American Thoracic Society
, vol.4
, Issue.4
, pp. 334-337
-
-
Corey, M.1
-
10
-
-
25444454574
-
The precision of longitudinal lung function measurements: Monitoring and interpretation
-
DOI 10.1136/oem.2004.018424
-
Hnizdo E, Yu L, Freyder L, et al. The precision of longitudinal lung function measurements: monitoring and interpretation. Occup Environ Med 2005;62:695-701. (Pubitemid 41360895)
-
(2005)
Occupational and Environmental Medicine
, vol.62
, Issue.10
, pp. 695-701
-
-
Hnizdo, E.1
Yu, L.2
Freyder, L.3
Attfield, M.4
Lefante, J.5
Glindmeyer, H.W.6
-
11
-
-
34548262715
-
Poor airway function in early infancy and lung function by age 22 years: A non-selective longitudinal cohort study
-
DOI 10.1016/S0140-6736(07)61379-8, PII S0140673607613798
-
Stern DA, Morgan WJ, Wright AL, et al. Poor airway function in early infancy and lung function by age 22 years: a non-selective longitudinal cohort study. Lancet 2007;370:758-64. (Pubitemid 47320800)
-
(2007)
Lancet
, vol.370
, Issue.9589
, pp. 758-764
-
-
Stern, D.A.1
Morgan, W.J.2
Wright, A.L.3
Guerra, S.4
Martinez, F.D.5
-
12
-
-
79955148832
-
Genetic variation in TIMP1 but not MMPs predict excess FEV1 decline in two general population-based cohorts
-
van Diemen C, Postma D, Siedlinski M, et al. Genetic variation in TIMP1 but not MMPs predict excess FEV1 decline in two general population-based cohorts. Respir Res 2011;12:57.
-
(2011)
Respir Res
, vol.12
, pp. 57
-
-
Van Diemen, C.1
Postma, D.2
Siedlinski, M.3
-
13
-
-
36248973150
-
Effect of occupational exposures on decline of lung function in early chronic obstructive pulmonary disease
-
DOI 10.1164/rccm.200605-730OC
-
Harber P, Tashkin DP, Simmons M, et al. Effect of occupational exposures on decline of lung function in early chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2007;176:994-1000. (Pubitemid 350127843)
-
(2007)
American Journal of Respiratory and Critical Care Medicine
, vol.176
, Issue.10
, pp. 994-1000
-
-
Harber, P.1
Tashkin, D.P.2
Simmons, M.3
Crawford, L.4
Hnizdo, E.5
Connett, J.6
-
14
-
-
0031471090
-
Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis
-
DOI 10.1016/S0022-3476(97)70025-8
-
Corey M, Edwards L, Levison H, et al. Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis. J Pediatr 1997;131:809-14. (Pubitemid 28027602)
-
(1997)
Journal of Pediatrics
, vol.131
, Issue.6
, pp. 809-814
-
-
Corey, M.1
Edwards, L.2
Levison, H.3
Knowles, M.4
-
16
-
-
21744460289
-
Standardisation of spirometry
-
DOI 10.1183/09031936.05.00034805
-
Miller MR, Hankinson J, Brusasco V, et al. Standardisation of spirometry. Eur Respir J 2005;26:319-38. (Pubitemid 41079078)
-
(2005)
European Respiratory Journal
, vol.26
, Issue.2
, pp. 319-338
-
-
Miller, M.R.1
Hankinson, J.2
Brusasco, V.3
Burgos, F.4
Casaburi, R.5
Coates, A.6
Crapo, R.7
Enright, P.8
Van Der Grinten, C.P.M.9
Gustafsson, P.10
Jensen, R.11
Johnson, D.C.12
MacIntrye, N.13
McKay, R.14
Navajas, D.15
Pedersen, O.F.16
Pellegrino, R.17
Viegi, G.18
Wagner, J.19
-
17
-
-
0027551290
-
Pulmonary function between 6 and 18 years of age
-
Wang X, Dockery DW, Wypij D, et al. Pulmonary function between 6 and 18 years of age. Pediatr Pulmonol 1993;15:75-88.
-
(1993)
Pediatr Pulmonol
, vol.15
, pp. 75-88
-
-
Wang, X.1
Dockery, D.W.2
Wypij, D.3
-
20
-
-
0020333131
-
Random-effects models for longitudinal data
-
Laird NM, Ware JH. Random-effects models for longitudinal data. Biometrics 1982;38:963-74.
-
(1982)
Biometrics
, vol.38
, pp. 963-974
-
-
Laird, N.M.1
Ware, J.H.2
-
21
-
-
1642534562
-
The Repeatability of Forced Expiratory Volume Measurements in Adults with Cystic Fibrosis
-
DOI 10.1378/chest.125.1.150
-
Stanbrook MB, Corey M, Tullis DE. The repeatability of forced expiratory volume measurements in adults with cystic fibrosis. Chest 2004;125:150-5. (Pubitemid 38114577)
-
(2004)
Chest
, vol.125
, Issue.1
, pp. 150-155
-
-
Stanbrook, M.B.1
Corey, M.2
Tullis, D.E.3
-
22
-
-
0016811540
-
Variability of routine pulmonary function tests
-
Hruby J, Butler J. Variability of routine pulmonary function tests. Thorax 1975;30:548-53.
-
(1975)
Thorax
, vol.30
, pp. 548-553
-
-
Hruby, J.1
Butler, J.2
-
23
-
-
0019387335
-
Changes in measured spirometric indices. What is significant?
-
Pennock BE, Rogers RM, McCaffree DR. Changes in measured spirometric indices. What is significant? Chest 1981;80:97-9. (Pubitemid 11002843)
-
(1981)
Chest
, vol.80
, Issue.1
, pp. 97-99
-
-
Pennock, B.E.1
Rogers, R.M.2
McCaffree, D.R.3
-
24
-
-
0024985943
-
Variability of pulmonary function tests in cystic fibrosis
-
Cooper PJ, Robertson CF, Hudson IL, et al. Variability of pulmonary function tests in cystic fibrosis. Pediatr Pulmonol 1990;8:16-22.
-
(1990)
Pediatr Pulmonol
, vol.8
, pp. 16-22
-
-
Cooper, P.J.1
Robertson, C.F.2
Hudson, I.L.3
-
25
-
-
1642575366
-
Repeatability of Spirometry in 18,000 Adult Patients
-
DOI 10.1164/rccm.200204-347OC
-
Enright PL, Beck KC, Sherrill DL. Repeatability of spirometry in 18,000 adult patients. Am J Respir Crit Care Med 2004;169:235-8. (Pubitemid 38114540)
-
(2004)
American Journal of Respiratory and Critical Care Medicine
, vol.169
, Issue.2
, pp. 235-238
-
-
Enright, P.L.1
Beck, K.C.2
Sherrill, D.L.3
-
26
-
-
55049140569
-
Annual assessment spirometry, plethysmography, and gas transfer in cystic fibrosis: Do they predict death or transplantation
-
Rosenthal M. Annual assessment spirometry, plethysmography, and gas transfer in cystic fibrosis: do they predict death or transplantation. Pediatr Pulmonol 2008;43:945-52.
-
(2008)
Pediatr Pulmonol
, vol.43
, pp. 945-952
-
-
Rosenthal, M.1
-
27
-
-
0033806235
-
Allergic bronchopulmonary aspergillosis in cystic fibrosis. A European epidemiological study. Epidemiologic Registry of Cystic Fibrosis
-
Mastella G, Rainisio M, Harms HK, et al . Allergic bronchopulmonary aspergillosis in cystic fibrosis. A European epidemiological study. Epidemiologic Registry of Cystic Fibrosis. Eur Respir J 2000;16:464-71.
-
(2000)
Eur Respir J
, vol.16
, pp. 464-471
-
-
Mastella, G.1
Rainisio, M.2
Harms, H.K.3
-
28
-
-
67949095989
-
Characterizing aggressiveness and predicting future progression of CF lung disease
-
Konstan MW, Wagener JS, VanDevanter DR. Characterizing aggressiveness and predicting future progression of CF lung disease. J Cyst Fibros 2009;8(Suppl 1): S15-19.
-
(2009)
J Cyst Fibros
, vol.8
, Issue.SUPPL. 1
-
-
Konstan, M.W.1
Wagener, J.S.2
VanDevanter, D.R.3
-
29
-
-
78649662363
-
Pulmonary outcome prediction (POP) tools for cystic fibrosis patients
-
Vandevanter DR, Wagener JS, Pasta DJ, et al. Pulmonary outcome prediction (POP) tools for cystic fibrosis patients. Pediatr Pulmonol 2010;45:1156-66.
-
(2010)
Pediatr Pulmonol
, vol.45
, pp. 1156-1166
-
-
Vandevanter, D.R.1
Wagener, J.S.2
Pasta, D.J.3
-
30
-
-
0026316543
-
Cystic fibrosis: Current survival and population estimates to the year 2000
-
Elborn JS, Shale DJ, Britton JR. Cystic fibrosis: current survival and population estimates to the year 2000. Thorax 1991;46:881-5.
-
(1991)
Thorax
, vol.46
, pp. 881-885
-
-
Elborn, J.S.1
Shale, D.J.2
Britton, J.R.3
-
31
-
-
0033614639
-
Long-term effect of inhaled budesonide in mild and moderate chronic obstructive pulmonary disease: A randomised controlled trial
-
DOI 10.1016/S0140-6736(98)10019-3
-
Vestbo J, Sorensen T, Lange P, et al. Long-term effect of inhaled budesonide in mild and moderate chronic obstructive pulmonary disease: a randomised controlled trial. Lancet 1999;353:1819-23. (Pubitemid 29251012)
-
(1999)
Lancet
, vol.353
, Issue.9167
, pp. 1819-1823
-
-
Vestbo, J.1
Sorensen, T.2
Lange, P.3
Brix, A.4
Tone, P.5
Viskum, K.6
-
32
-
-
57349180789
-
Longitudinal decline in lung volume in a population of children with sickle cell disease
-
MacLean JE, Atenafu E, Kirby-Allen M, et al. Longitudinal decline in lung volume in a population of children with sickle cell disease. Am J Respir Crit Care Med 2008;178:1055-9.
-
(2008)
Am J Respir Crit Care Med
, vol.178
, pp. 1055-1059
-
-
MacLean, J.E.1
Atenafu, E.2
Kirby-Allen, M.3
-
33
-
-
67649777117
-
The natural history of chronic airflow obstruction revisited: An analysis of the Framingham offspring cohort
-
Kohansal R, Martinez-Camblor P, Agusti A, et al. The natural history of chronic airflow obstruction revisited: an analysis of the Framingham offspring cohort. Am J Respir Crit Care Med 2009;180:3-10.
-
(2009)
Am J Respir Crit Care Med
, vol.180
, pp. 3-10
-
-
Kohansal, R.1
Martinez-Camblor, P.2
Agusti, A.3
-
34
-
-
0029921514
-
Improved survival in the Danish center-treated cystic fibrosis patients: Results of aggressive treatment
-
DOI 10.1002/(SICI)1099-0496(199603)21:3<153::AID-PPUL1>3.0.CO;2-R
-
Frederiksen B, Lanng S, Koch C, et al. Improved survival in the Danish center-treated cystic fibrosis patients: results of aggressive treatment. Pediatr Pulmonol 1996;21:153-8. (Pubitemid 26127307)
-
(1996)
Pediatric Pulmonology
, vol.21
, Issue.3
, pp. 153-158
-
-
Frederiksen, B.1
Lanng, S.2
Koch, C.3
Hoiby, N.4
|