-
1
-
-
0031950258
-
Risk of death in cystic fibrosis patients with severely compromised lung function
-
Milla CE, Warwick WJ. Risk of death in cystic fibrosis patients with severely compromised lung function. Chest 1998;113:1230-4.
-
(1998)
Chest
, vol.113
, pp. 1230-1234
-
-
Milla, C.E.1
Warwick, W.J.2
-
2
-
-
4143080355
-
Lung function decline in cystic fibrosis patients and timing for lung transplantation referral
-
Rosenbluth DB, Wilson K, Ferkol T, et al. Lung function decline in cystic fibrosis patients and timing for lung transplantation referral. Chest 2004;126:412-9.
-
(2004)
Chest
, vol.126
, pp. 412-419
-
-
Rosenbluth, D.B.1
Wilson, K.2
Ferkol, T.3
-
3
-
-
17944371749
-
Prediction of mortality and timing of referral for lung transplantation in cystic Fibrosis patients
-
Augarten A, Akons H, Aviram M, et al. Prediction of mortality and timing of referral for lung transplantation in cystic Fibrosis patients. Pediatr Transplant 2001;5:339-42.
-
(2001)
Pediatr Transplant
, vol.5
, pp. 339-342
-
-
Augarten, A.1
Akons, H.2
Aviram, M.3
-
4
-
-
0031021662
-
Identifying treatments that halt progression of pulmonary disease in cystic fibrosis
-
Davis PB, Byard PJ, Konstan MW. Identifying treatments that halt progression of pulmonary disease in cystic fibrosis. Pediatr Res 1997;41:161-5.
-
(1997)
Pediatr Res
, vol.41
, pp. 161-165
-
-
Davis, P.B.1
Byard, P.J.2
Konstan, M.W.3
-
5
-
-
0028914667
-
Effect of high-dose ibuprofen in patients with cystic fibrosis
-
Konstan MW, Byard PJ, Hoppel CL, et al. Effect of high-dose ibuprofen in patients with cystic fibrosis. N Engl J Med 1995;332:848-54.
-
(1995)
N Engl J Med
, vol.332
, pp. 848-854
-
-
Konstan, M.W.1
Byard, P.J.2
Hoppel, C.L.3
-
6
-
-
0027287651
-
Efficacy of aerosolized tobramycin in patients with cystic fibrosis
-
Ramsey BW, Dorkin ML, Eisenberg JD, et al. Efficacy of aerosolized tobramycin in patients with cystic fibrosis. N Engl J Med 1993;328:1740-6.
-
(1993)
N Engl J Med
, vol.328
, pp. 1740-1746
-
-
Ramsey, B.W.1
Dorkin, M.L.2
Eisenberg, J.D.3
-
7
-
-
0017097945
-
Five- to seven-year course of pulmonary function in cystic fibrosis
-
Corey M, Levison H, Crozier D. Five- to seven-year course of pulmonary function in cystic fibrosis. Am Rev Respir Dis 1976;114:1085-92.
-
(1976)
Am Rev Respir Dis
, vol.114
, pp. 1085-1092
-
-
Corey, M.1
Levison, H.2
Crozier, D.3
-
8
-
-
0025355607
-
Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa
-
Kerem E, Corey M, Gold R, et al. Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa. J Pediatr 1990;116:714-9.
-
(1990)
J Pediatr
, vol.116
, pp. 714-719
-
-
Kerem, E.1
Corey, M.2
Gold, R.3
-
9
-
-
0027331557
-
Passive smoking and lung function in cystic fibrosis
-
Kovesi T, Corey M, Levison H. Passive smoking and lung function in cystic fibrosis. Am Rev Respir Dis 1993;148:1266-71.
-
(1993)
Am Rev Respir Dis
, vol.148
, pp. 1266-1271
-
-
Kovesi, T.1
Corey, M.2
Levison, H.3
-
10
-
-
0028969594
-
A multicenter study of alternate-day prednisone therapy in patients with cystic fibrosis
-
Eigen H, Rosenstein B, FitzSimmons S, et al. A multicenter study of alternate-day prednisone therapy in patients with cystic fibrosis. J Pediatr 1995;126:515-23.
-
(1995)
J Pediatr
, vol.126
, pp. 515-523
-
-
Eigen, H.1
Rosenstein, B.2
Fitzsimmons, S.3
-
11
-
-
0031471090
-
Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis
-
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.
-
(1997)
J Pediatr
, vol.131
, pp. 809-814
-
-
Corey, M.1
Edwards, L.2
Levison, H.3
-
12
-
-
0033825741
-
Trends in pulmonary function in patients with cystic fibrosis correlate with the degree or glucose intolerance at baseline
-
Milla CE, Warwick WJ, Moran A. Trends in pulmonary function in patients with cystic fibrosis correlate with the degree or glucose intolerance at baseline. Am J Respir Crit Care Med 2000;162:891-5.
-
(2000)
Am J Respir Crit Care Med
, vol.162
, pp. 891-895
-
-
Milla, C.E.1
Warwick, W.J.2
Moran, A.3
-
13
-
-
0036014532
-
Annual lung function changes in young patients with chronic lung disease
-
Merkus PJ, Tiddens HA, de Jongste JC. Annual lung function changes in young patients with chronic lung disease. Eur Respir J 2002;19:886-91.
-
(2002)
Eur Respir J
, vol.19
, pp. 886-891
-
-
Merkus, P.J.1
Tiddens, H.A.2
De Jongste, J.C.3
-
14
-
-
0347363613
-
Preserved diffusion capacity in children with cystic fibrosis
-
Merkus PJ, Govaere ES, Hop WH, et al. Preserved diffusion capacity in children with cystic fibrosis. Pediatr Pulmonol 2004;37:56-60.
-
(2004)
Pediatr Pulmonol
, vol.37
, pp. 56-60
-
-
Merkus, P.J.1
Govaere, E.S.2
Hop, W.H.3
-
15
-
-
4143080355
-
Lung function decline in cystic fibrosis patients and timing for lung transplantation referral
-
Rosenbluth DB, Wilson K, Ferkol T, et al. Lung function decline in cystic fibrosis patients and timing for lung transplantation referral. Chest 2004;126:412-9.
-
(2004)
Chest
, vol.126
, pp. 412-419
-
-
Rosenbluth, D.B.1
Wilson, K.2
Ferkol, T.3
-
16
-
-
17944371749
-
Prediction of mortality and timing of referral for lung transplantation in cystic fibrosis patients
-
Augarten A, Akons H, Aviram M, et al. Prediction of mortality and timing of referral for lung transplantation in cystic fibrosis patients. Pediatr Transplant 2001;5:339-42.
-
(2001)
Pediatr Transplant
, vol.5
, pp. 339-342
-
-
Augarten, A.1
Akons, H.2
Aviram, M.3
-
17
-
-
0036112237
-
Predictors of deterioration of lung function in cystic fibrosis
-
Schaedel C, De Monestrol I, Hjelte L, et al. Predictors of deterioration of lung function in cystic fibrosis. Pediatr Pulmonol 2002;33:483-91.
-
(2002)
Pediatr Pulmonol
, vol.33
, pp. 483-491
-
-
Schaedel, C.1
De Monestrol, I.2
Hjelte, L.3
-
18
-
-
0034785481
-
Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition
-
Kosorok MR, Zeng L, West SE, et al. Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition. Pediatr Pulmonol 2001;32:277-87.
-
(2001)
Pediatr Pulmonol
, vol.32
, pp. 277-287
-
-
Kosorok, M.R.1
Zeng, L.2
West, S.E.3
-
19
-
-
32544459013
-
Changing patterns of lung function decline in children with cystic fibrosis
-
Xu W, Subbarao P, Corey M. Changing patterns of lung function decline in children with cystic fibrosis. J Cystic Fibrosis 2004;3:S116.
-
(2004)
J Cystic Fibrosis
, vol.3
-
-
Xu, W.1
Subbarao, P.2
Corey, M.3
-
20
-
-
0142030262
-
Does dornase alfa make any difference?
-
The European Epidemiologic Registry of Cystic Fibrosis (ERCF). Berlin: European CF Conference
-
Hodson ME, Koch C, Harries HK, et al. The European Epidemiologic Registry of Cystic Fibrosis (ERCF). Does dornase alfa make any difference? In: Proceedings of the 22nd European CF Conference, Berlin, Germany. Berlin: European CF Conference, 1998:66.
-
(1998)
Proceedings of the 22nd European CF Conference, Berlin, Germany
, pp. 66
-
-
Hodson, M.E.1
Koch, C.2
Harries, H.K.3
|