-
1
-
-
70349507503
-
Healthcare expenditures for privately insured people with cystic fibrosis
-
Ouyang L., Grosse S.D., Amendah D.D., Schechter M.S. Healthcare expenditures for privately insured people with cystic fibrosis. Pediatr Pulmonol 2009, 44:989-996.
-
(2009)
Pediatr Pulmonol
, vol.44
, pp. 989-996
-
-
Ouyang, L.1
Grosse, S.D.2
Amendah, D.D.3
Schechter, M.S.4
-
2
-
-
0025095907
-
Quality of well-being before and after antibiotic treatment of pulmonary exacerbation in patients with cystic fibrosis
-
Orenstein D.M., Pattishall E.N., Nixon P.A., Ross E.A., Kaplan R.M. Quality of well-being before and after antibiotic treatment of pulmonary exacerbation in patients with cystic fibrosis. Chest 1990, 98:1081-1084.
-
(1990)
Chest
, vol.98
, pp. 1081-1084
-
-
Orenstein, D.M.1
Pattishall, E.N.2
Nixon, P.A.3
Ross, E.A.4
Kaplan, R.M.5
-
3
-
-
0035000956
-
Pulmonary function, inflammation, exercise capacity and quality of life in cystic fibrosis
-
Bradley J., McAlister O., Elborn S. Pulmonary function, inflammation, exercise capacity and quality of life in cystic fibrosis. Eur Respir J 2001, 17:712-715.
-
(2001)
Eur Respir J
, vol.17
, pp. 712-715
-
-
Bradley, J.1
McAlister, O.2
Elborn, S.3
-
4
-
-
0036152764
-
Impact of recent pulmonary exacerbations on quality of life in patients with cystic fibrosis
-
Britto M.T., Kotagal U.R., Hornung R.W., Atherton H.D., Tsevat J., Wilmott R.W. Impact of recent pulmonary exacerbations on quality of life in patients with cystic fibrosis. Chest 2002, 121:64-72.
-
(2002)
Chest
, vol.121
, pp. 64-72
-
-
Britto, M.T.1
Kotagal, U.R.2
Hornung, R.W.3
Atherton, H.D.4
Tsevat, J.5
Wilmott, R.W.6
-
5
-
-
33344468629
-
Cystic fibrosis pulmonary exacerbations
-
Ferkol T., Rosenfeld M., Milla C.E. Cystic fibrosis pulmonary exacerbations. J Pediatr 2006, 148:259-264.
-
(2006)
J Pediatr
, vol.148
, pp. 259-264
-
-
Ferkol, T.1
Rosenfeld, M.2
Milla, C.E.3
-
6
-
-
75849154666
-
Return of FEV(1) after pulmonary exacerbation in children with cystic fibrosis
-
Sanders D.B., Hoffman L.R., Emerson J., et al. Return of FEV(1) after pulmonary exacerbation in children with cystic fibrosis. Pediatr Pulmonol 2010, 45:127-134.
-
(2010)
Pediatr Pulmonol
, vol.45
, pp. 127-134
-
-
Sanders, D.B.1
Hoffman, L.R.2
Emerson, J.3
-
7
-
-
0035865730
-
Predictive 5-year survivorship model of cystic fibrosis
-
Liou T.G., Adler F.R., Fitzsimmons S.C., Cahill B.C., Hibbs J.R., Marshall B.C. Predictive 5-year survivorship model of cystic fibrosis. Am J Epidemiol 2001, 153:345-352.
-
(2001)
Am J Epidemiol
, vol.153
, pp. 345-352
-
-
Liou, T.G.1
Adler, F.R.2
Fitzsimmons, S.C.3
Cahill, B.C.4
Hibbs, J.R.5
Marshall, B.C.6
-
8
-
-
0037115262
-
Developing cystic fibrosis lung transplant referral criteria using predictors of 2-year mortality
-
Mayer-Hamblett N., Rosenfeld M., Emerson J., Goss C.H., Aitken M.L. Developing cystic fibrosis lung transplant referral criteria using predictors of 2-year mortality. Am J Respir Crit Care Med 2002, 166:1550-1555.
-
(2002)
Am J Respir Crit Care Med
, vol.166
, pp. 1550-1555
-
-
Mayer-Hamblett, N.1
Rosenfeld, M.2
Emerson, J.3
Goss, C.H.4
Aitken, M.L.5
-
9
-
-
0036320272
-
Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis
-
Emerson J., Rosenfeld M., McNamara S., Ramsey B., Gibson R.L. Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis. Pediatr Pulmonol 2002, 34:91-100.
-
(2002)
Pediatr Pulmonol
, vol.34
, pp. 91-100
-
-
Emerson, J.1
Rosenfeld, M.2
McNamara, S.3
Ramsey, B.4
Gibson, R.L.5
-
10
-
-
34147215995
-
Exacerbations in cystic fibrosis. 1: epidemiology and pathogenesis
-
Goss C.H., Burns J.L. Exacerbations in cystic fibrosis. 1: epidemiology and pathogenesis. Thorax 2007, 62:360-367.
-
(2007)
Thorax
, vol.62
, pp. 360-367
-
-
Goss, C.H.1
Burns, J.L.2
-
11
-
-
81255206186
-
Design and powering of cystic fibrosis clinical trials using pulmonary exacerbation as an efficacy endpoint
-
VanDevanter D.R., Yegin A., Morgan W.J., Millar S.J., Pasta D.J., Konstan M.W. Design and powering of cystic fibrosis clinical trials using pulmonary exacerbation as an efficacy endpoint. J Cyst Fibros 2011, 10:453-459.
-
(2011)
J Cyst Fibros
, vol.10
, pp. 453-459
-
-
VanDevanter, D.R.1
Yegin, A.2
Morgan, W.J.3
Millar, S.J.4
Pasta, D.J.5
Konstan, M.W.6
-
12
-
-
84879411129
-
Oral, inhaled, and intravenous antibiotic choice for treating pulmonary exacerbations in cystic fibrosis
-
[Epub ahead of print]
-
Wagener J.S., VanDevanter D.R., Regelmann W., et al. Oral, inhaled, and intravenous antibiotic choice for treating pulmonary exacerbations in cystic fibrosis. Pediatr Pulmonol Aug 8 2012, [Epub ahead of print]. 10.1002/ppul.22652.
-
(2012)
Pediatr Pulmonol
-
-
Wagener, J.S.1
VanDevanter, D.R.2
Regelmann, W.3
-
13
-
-
80051796005
-
Approach to treating cystic fibrosis pulmonary exacerbations varies widely across US CF care centers
-
Kraynack N.C., Gothard M.D., Falletta L.M., McBride J.T. Approach to treating cystic fibrosis pulmonary exacerbations varies widely across US CF care centers. Pediatr Pulmonol 2011, 46:870-881.
-
(2011)
Pediatr Pulmonol
, vol.46
, pp. 870-881
-
-
Kraynack, N.C.1
Gothard, M.D.2
Falletta, L.M.3
McBride, J.T.4
-
14
-
-
0028129568
-
Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group
-
Fuchs H.J., Borowitz D.S., Christiansen D.H., et al. Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group. N Engl J Med 1994, 331:637-642.
-
(1994)
N Engl J Med
, vol.331
, pp. 637-642
-
-
Fuchs, H.J.1
Borowitz, D.S.2
Christiansen, D.H.3
-
15
-
-
0035666058
-
A two-year randomized, placebo controlled trial of dornase alfa in young patients with cystic fibrosis with mild lung function abnormalities
-
Quan J.M., Tiddens H.A., Sy J.P., et al. A two-year randomized, placebo controlled trial of dornase alfa in young patients with cystic fibrosis with mild lung function abnormalities. J Pediatr 2001, 139:813-820.
-
(2001)
J Pediatr
, vol.139
, pp. 813-820
-
-
Quan, J.M.1
Tiddens, H.A.2
Sy, J.P.3
-
16
-
-
30944466084
-
A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis
-
Elkins M.R., Robinson M., Rose B.R., et al. A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. N Engl J Med 2006, 354:229-240.
-
(2006)
N Engl J Med
, vol.354
, pp. 229-240
-
-
Elkins, M.R.1
Robinson, M.2
Rose, B.R.3
-
17
-
-
44649166466
-
Inhaled mannitol improves lung function in cystic fibrosis
-
Jaques A., Daviskas E., Turton J.A., et al. Inhaled mannitol improves lung function in cystic fibrosis. Chest 2008, 133:1388-1396.
-
(2008)
Chest
, vol.133
, pp. 1388-1396
-
-
Jaques, A.1
Daviskas, E.2
Turton, J.A.3
-
18
-
-
0033531143
-
Intermittent administration of inhaled tobramycin in patients with cystic fibrosis
-
Ramsey B.W., Pepe M.S., Quan J.M., et al. Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. N Engl J Med 1999, 340:23-30.
-
(1999)
N Engl J Med
, vol.340
, pp. 23-30
-
-
Ramsey, B.W.1
Pepe, M.S.2
Quan, J.M.3
-
19
-
-
4544269731
-
Treatment with tobramycin solution for inhalation reduces hospitalizations in young CF subjects with mild lung disease
-
Murphy T.D., Anbar R.D., Lester L.A., Nasr S.Z., Nickerson B., VanDevanter D.R., et al. Treatment with tobramycin solution for inhalation reduces hospitalizations in young CF subjects with mild lung disease. Pediatr Pulmonol 2004, 38:314-320.
-
(2004)
Pediatr Pulmonol
, vol.38
, pp. 314-320
-
-
Murphy, T.D.1
Anbar, R.D.2
Lester, L.A.3
Nasr, S.Z.4
Nickerson, B.5
VanDevanter, D.R.6
-
20
-
-
55549137086
-
Inhaled aztreonam lysine for chronic airway Pseudomonas aeruginosa in cystic fibrosis
-
McCoy K.S., Quittner A.L., Oermann C.M., Gibson R.L., Retsch-Bogart G.Z., Montgomery A.B. Inhaled aztreonam lysine for chronic airway Pseudomonas aeruginosa in cystic fibrosis. Am J Respir Crit Care Med 2008, 178:921-928.
-
(2008)
Am J Respir Crit Care Med
, vol.178
, pp. 921-928
-
-
McCoy, K.S.1
Quittner, A.L.2
Oermann, C.M.3
Gibson, R.L.4
Retsch-Bogart, G.Z.5
Montgomery, A.B.6
-
21
-
-
0037190575
-
Long term azithromycin in children with cystic fibrosis: a randomised, placebo-controlled crossover trial
-
Equi A., Balfour-Lynn I.M., Bush A., Rosenthal M. Long term azithromycin in children with cystic fibrosis: a randomised, placebo-controlled crossover trial. Lancet 2002, 360:978-984.
-
(2002)
Lancet
, vol.360
, pp. 978-984
-
-
Equi, A.1
Balfour-Lynn, I.M.2
Bush, A.3
Rosenthal, M.4
-
22
-
-
0036185807
-
Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: a randomised trial
-
Wolter J., Seeney S., Bell S., Bowler S., Masel P., McCormack J. Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: a randomised trial. Thorax 2002, 57:212-216.
-
(2002)
Thorax
, vol.57
, pp. 212-216
-
-
Wolter, J.1
Seeney, S.2
Bell, S.3
Bowler, S.4
Masel, P.5
McCormack, J.6
-
23
-
-
0141816759
-
Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trial
-
Saiman L., Marshall B.C., Mayer-Hamblett N., et al. Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trial. JAMA 2003, 290:1749-1756.
-
(2003)
JAMA
, vol.290
, pp. 1749-1756
-
-
Saiman, L.1
Marshall, B.C.2
Mayer-Hamblett, N.3
-
24
-
-
78549279173
-
Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation
-
Accurso F.J., Rowe S.M., Clancy J.P., et al. Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation. N Engl J Med 2010, 363:1991-2003.
-
(2010)
N Engl J Med
, vol.363
, pp. 1991-2003
-
-
Accurso, F.J.1
Rowe, S.M.2
Clancy, J.P.3
-
25
-
-
80455162465
-
A CFTR potentiator in patients with cystic fibrosis and the G551D mutation
-
Ramsey B.W., Davies J., McElvaney N.G., et al. A CFTR potentiator in patients with cystic fibrosis and the G551D mutation. N Engl J Med 2011, 365:1663-1672.
-
(2011)
N Engl J Med
, vol.365
, pp. 1663-1672
-
-
Ramsey, B.W.1
Davies, J.2
McElvaney, N.G.3
-
26
-
-
78649647554
-
Trends in the use of routine therapies in cystic fibrosis: 1995-2005
-
Konstan M.W., VanDevanter D.R., Rasouliyan L., et al. Trends in the use of routine therapies in cystic fibrosis: 1995-2005. Pediatr Pulmonol 2010, 45:1167-1172.
-
(2010)
Pediatr Pulmonol
, vol.45
, pp. 1167-1172
-
-
Konstan, M.W.1
VanDevanter, D.R.2
Rasouliyan, L.3
-
27
-
-
70350446684
-
Cystic fibrosis pulmonary guidelines: treatment of pulmonary exacerbations
-
Flume P.A., Mogayzel P.J., Robinson K.A., et al. Cystic fibrosis pulmonary guidelines: treatment of pulmonary exacerbations. Am J Respir Crit Care Med 2009, 180:802-808.
-
(2009)
Am J Respir Crit Care Med
, vol.180
, pp. 802-808
-
-
Flume, P.A.1
Mogayzel, P.J.2
Robinson, K.A.3
-
28
-
-
69549135253
-
Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: a European consensus
-
consensus working group
-
Heijerman H., Westerman E., Conway S., Touw D., Döring G., consensus working group Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: a European consensus. J Cyst Fibros 2009, 8:295-315.
-
(2009)
J Cyst Fibros
, vol.8
, pp. 295-315
-
-
Heijerman, H.1
Westerman, E.2
Conway, S.3
Touw, D.4
Döring, G.5
-
29
-
-
49649113873
-
Trends in the clinical characteristics of the U.S. cystic fibrosis patient population from 1995 to 2005
-
VanDevanter D.R., Rasouliyan L.H., Murphy T.M., et al. Trends in the clinical characteristics of the U.S. cystic fibrosis patient population from 1995 to 2005. Pediatr Pulmonol 2008, 43:739-744.
-
(2008)
Pediatr Pulmonol
, vol.43
, pp. 739-744
-
-
VanDevanter, D.R.1
Rasouliyan, L.H.2
Murphy, T.M.3
-
31
-
-
13044254788
-
Epidemiologic study of cystic fibrosis: design and implementation of a prospective, multicenter, observational study of patients with cystic fibrosis in the U.S. and Canada
-
Morgan W.J., Butler S.M., Johnson C.A., et al. Epidemiologic study of cystic fibrosis: design and implementation of a prospective, multicenter, observational study of patients with cystic fibrosis in the U.S. and Canada. Pediatr Pulmonol 1999, 28:231-241.
-
(1999)
Pediatr Pulmonol
, vol.28
, pp. 231-241
-
-
Morgan, W.J.1
Butler, S.M.2
Johnson, C.A.3
-
32
-
-
2442480846
-
Pulmonary exacerbations in cystic fibrosis
-
Rabin H.R., Butler S.M., Wohl M.E., et al. Pulmonary exacerbations in cystic fibrosis. Pediatr Pulmonol 2004, 37:400-406.
-
(2004)
Pediatr Pulmonol
, vol.37
, pp. 400-406
-
-
Rabin, H.R.1
Butler, S.M.2
Wohl, M.E.3
|