-
2
-
-
0032869672
-
Patterns of medical practice in cystic fibrosis: Part II. Use of therapies. Investigators and coordinators of the epidemiologic study of cystic fibrosis
-
Konstan MW, Butler SM, Schidlow DV, Morgan WJ, Julius JR, et al. (1999) Patterns of medical practice in cystic fibrosis: part II. Use of therapies. Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Pediatr Pulmonol 28: 248-254.
-
(1999)
Pediatr Pulmonol
, vol.28
, pp. 248-254
-
-
Konstan, M.W.1
Butler, S.M.2
Schidlow, D.V.3
Morgan, W.J.4
Julius, J.R.5
-
3
-
-
0037252230
-
Factors influencing outcomes in cystic fibrosis: A center-based analysis
-
Johnson C, Butler SM, Konstan MW, Morgan W, Wohl ME (2003) Factors influencing outcomes in cystic fibrosis: a center-based analysis. Chest 123: 20-27.
-
(2003)
Chest
, vol.123
, pp. 20-27
-
-
Johnson, C.1
Butler, S.M.2
Konstan, M.W.3
Morgan, W.4
Wohl, M.E.5
-
4
-
-
0142074349
-
Long-acting bronchodilators in cystic fibrosis
-
Colombo JL (2003) Long-acting bronchodilators in cystic fibrosis. Curr Opin Pulm Med 9: 504-508.
-
(2003)
Curr Opin Pulm Med
, vol.9
, pp. 504-508
-
-
Colombo, J.L.1
-
5
-
-
84882554669
-
Effectiveness of bronchodilators in cystic fibrosis
-
Cropp GJ (1996) Effectiveness of bronchodilators in cystic fibrosis. Am J Med 100: 19S-29S.
-
(1996)
Am J Med
, vol.100
, pp. 19S-29S
-
-
Cropp, G.J.1
-
6
-
-
0026858516
-
Efficacy of salbutamol and ipratropium bromide in decreasing bronchial hyperreactivity in children with cystic fibrosis
-
Avital A, Sanchez I, Chernick V (1992) Efficacy of salbutamol and ipratropium bromide in decreasing bronchial hyperreactivity in children with cystic fibrosis. Pediatr Pulmonol 13: 34-37.
-
(1992)
Pediatr Pulmonol
, vol.13
, pp. 34-37
-
-
Avital, A.1
Sanchez, I.2
Chernick, V.3
-
7
-
-
36448952390
-
A randomized study of tiotropium respimat soft mist inhaler vs. ipratropium pMDI in COPD
-
Voshaar T, Lapidus R, Maleki-Yazdi R, Timmer W, Rubin E, et al. (2008) A randomized study of tiotropium Respimat Soft Mist inhaler vs. ipratropium pMDI in COPD. Respir Med 102: 32-41.
-
(2008)
Respir Med
, vol.102
, pp. 32-41
-
-
Voshaar, T.1
Lapidus, R.2
Maleki-Yazdi, R.3
Timmer, W.4
Rubin, E.5
-
8
-
-
77956340477
-
Efficacy and safety of tiotropium respimat SMI in COPD in two 1-year randomized studies
-
Bateman E, Singh D, Smith D, Disse B, Towse L, et al. (2010) Efficacy and safety of tiotropium Respimat SMI in COPD in two 1-year randomized studies. Int J Chron Obstruct Pulmon Dis 5: 197-208.
-
(2010)
Int J Chron Obstruct Pulmon Dis
, vol.5
, pp. 197-208
-
-
Bateman, E.1
Singh, D.2
Smith, D.3
Disse, B.4
Towse, L.5
-
9
-
-
84907093606
-
Children below five years of age can handle respimat soft mist inhaler [abstract]
-
Kamin W, Bannemer-Schult K, Klemmer A, Schulze Schweinhorst P, Wachtel H, et al. (2010) Children below five years of age can handle Respimat Soft Mist inhaler [abstract]. Am J Respir Crit Care Med 181 A6254.
-
(2010)
Am J Respir Crit Care Med
, vol.181
, pp. A6254
-
-
Kamin, W.1
Bannemer-Schult, K.2
Klemmer, A.3
Schulze Schweinhorst, P.4
Wachtel, H.5
-
10
-
-
84922548158
-
Flow profile data indicate that respimat with spacer is suitable for inhalation therapy of pre-school children
-
18-22 June 2011; Rotterdam, The Netherlands
-
Kamin W, Bannemer-Schult K, Klemmer A, Schulze Schweinhorst P, Wachtel H, et al. (2011) Flow profile data indicate that Respimat with spacer is suitable for inhalation therapy of pre-school children. Presented at: International Society for Aerosols in Medicine Congress; 18-22 June 2011; Rotterdam, The Netherlands.
-
(2011)
International Society for Aerosols in Medicine Congress
-
-
Kamin, W.1
Bannemer-Schult, K.2
Klemmer, A.3
Schulze Schweinhorst, P.4
Wachtel, H.5
-
11
-
-
47049115524
-
Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic fibrosis foundation consensus report
-
Farrell PM, Rosenstein BJ, White TB, Accurso FJ, Castellani C, et al. (2008) Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report. J Pediatr 153: S4-S14.
-
(2008)
J Pediatr
, vol.153
, pp. S4-S14
-
-
Farrell, P.M.1
Rosenstein, B.J.2
White, T.B.3
Accurso, F.J.4
Castellani, C.5
-
12
-
-
0027752448
-
Pulmonary function growth velocity in children 6 to 18 years of age
-
Wang X, Dockery DW, Wypij D, Gold DR, Speizer FE, et al. (1993) Pulmonary function growth velocity in children 6 to 18 years of age. Am Rev Respir Dis 148: 1502-1508.
-
(1993)
Am Rev Respir Dis
, vol.148
, pp. 1502-1508
-
-
Wang, X.1
Dockery, D.W.2
Wypij, D.3
Gold, D.R.4
Speizer, F.E.5
-
13
-
-
0020585150
-
Changes in the normal maximal expiratory flow-volume curve with growth and aging
-
Knudson RJ, Lebowitz MD, Holberg CJ, Burrows B (1983) Changes in the normal maximal expiratory flow-volume curve with growth and aging. Am Rev Respir Dis 127: 725-734.
-
(1983)
Am Rev Respir Dis
, vol.127
, pp. 725-734
-
-
Knudson, R.J.1
Lebowitz, M.D.2
Holberg, C.J.3
Burrows, B.4
-
14
-
-
0037320133
-
Development of the cystic fibrosis questionnaire (CFQ) for assessing quality of life in pediatric and adult patients
-
Henry B, Aussage P, Grosskopf C, Goehrs JM (2003) Development of the Cystic Fibrosis Questionnaire (CFQ) for assessing quality of life in pediatric and adult patients. Qual Life Res 12: 63-76.
-
(2003)
Qual Life Res
, vol.12
, pp. 63-76
-
-
Henry, B.1
Aussage, P.2
Grosskopf, C.3
Goehrs, J.M.4
-
15
-
-
21744460289
-
Standardisation of spirometry
-
Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, et al. (2005) Standardisation of spirometry. Eur Respir J 26: 319-338.
-
(2005)
Eur Respir J
, vol.26
, pp. 319-338
-
-
Miller, M.R.1
Hankinson, J.2
Brusasco, V.3
Burgos, F.4
Casaburi, R.5
-
17
-
-
34147215995
-
Exacerbations in cystic fibrosis. 1: Epidemiology and pathogenesis
-
Goss CH, Burns JL (2007) Exacerbations in cystic fibrosis. 1: Epidemiology and pathogenesis. Thorax 62: 360-367.
-
(2007)
Thorax
, vol.62
, pp. 360-367
-
-
Goss, C.H.1
Burns, J.L.2
-
18
-
-
84895070149
-
Pulmonary exacerbations in a phase 2 clinical trial of BIIL 284 BS in CF: Development and implementation of a respiratory and systemic symptoms questionnaire (RSSQ)
-
[abstract]
-
Lymp J (2009) Pulmonary exacerbations in a phase 2 clinical trial of BIIL 284 BS in CF: development and implementation of a respiratory and systemic symptoms questionnaire (RSSQ) [abstract]. Pediatr Pulmonol S23 A221.
-
(2009)
Pediatr Pulmonol
, Issue.S23
, pp. A221
-
-
Lymp, J.1
-
19
-
-
85067711023
-
A randomized, double-blind, placebo controlled study to investigate the efficacy and safety of 24 weeks of oral treatment with BIIL 284 BS in adult (75 mg, 150 mg) and pediatric (75 mg) cystic fibrosis patients
-
Koker P, Bhattacharya S, Staab A (2007) A randomized, double-blind, placebo controlled study to investigate the efficacy and safety of 24 weeks of oral treatment with BIIL 284 BS in adult (75 mg, 150 mg) and pediatric (75 mg) cystic fibrosis patients. Boeringher Ingelheim Report.
-
(2007)
Boeringher Ingelheim Report
-
-
Koker, P.1
Bhattacharya, S.2
Staab, A.3
-
20
-
-
0037587546
-
The CONSORT statement: Revised recommendations for improving the quality of reports of parallel group randomized trials
-
Moher D, Schulz KF, Altman DG (2001) The CONSORT statement: revised recommendations for improving the quality of reports of parallel group randomized trials. BMC Med Res Methodol 1: 2.
-
(2001)
BMC Med Res Methodol
, vol.1
, pp. 2
-
-
Moher, D.1
Schulz, K.F.2
Altman, D.G.3
-
21
-
-
84907093605
-
Tiotropium respimat in cystic fibrosis: Efficacy and safety results of phase III randomized placebo-controlled trial [abstract]
-
Ratjen F, Koker P, Geller D, Langellier-Cocteaux B, Maulf F Le, et al. (2013) Tiotropium Respimat in cystic fibrosis: efficacy and safety results of phase III randomized placebo-controlled trial [abstract]. J Cyst Fibros (Suppl 1): S64.
-
(2013)
J Cyst Fibros
, pp. S64
-
-
Ratjen, F.1
Koker, P.2
Geller, D.3
Langellier-Cocteaux, B.4
Le, M.F.5
-
23
-
-
0032947760
-
Effects of standard and high doses of salmeterol on lung function of hospitalized patients with cystic fibrosis
-
Hordvik NL, Sammut PH, Judy CG, Colombo JL (1999) Effects of standard and high doses of salmeterol on lung function of hospitalized patients with cystic fibrosis. Pediatr Pulmonol 27: 43-53.
-
(1999)
Pediatr Pulmonol
, vol.27
, pp. 43-53
-
-
Hordvik, N.L.1
Sammut, P.H.2
Judy, C.G.3
Colombo, J.L.4
-
24
-
-
0036298101
-
Effects of salmeterol on arterial oxyhemoglobin saturations in patients with cystic fibrosis
-
Salvatore D, D'Andria M (2002) Effects of salmeterol on arterial oxyhemoglobin saturations in patients with cystic fibrosis. Pediatr Pulmonol 34: 11-15.
-
(2002)
Pediatr Pulmonol
, vol.34
, pp. 11-15
-
-
Salvatore, D.1
D'Andria, M.2
-
25
-
-
0036785093
-
Effectiveness and tolerability of high-dose salmeterol in cystic fibrosis
-
Hordvik NL, Sammut PH, Judy CG, Colombo JL (2002) Effectiveness and tolerability of high-dose salmeterol in cystic fibrosis. Pediatr Pulmonol 34: 287-296.
-
(2002)
Pediatr Pulmonol
, vol.34
, pp. 287-296
-
-
Hordvik, N.L.1
Sammut, P.H.2
Judy, C.G.3
Colombo, J.L.4
-
26
-
-
73749084119
-
Tiotropium 5 μg via respimat and 18 μg via handiHaler; efficacy and safety in Japanese COPD patients
-
Ichinose M, Fujimoto T, Fukuchi Y (2010) Tiotropium 5 μg via Respimat and 18 μg via HandiHaler; efficacy and safety in Japanese COPD patients. Respir Med 104: 228-236.
-
(2010)
Respir Med
, vol.104
, pp. 228-236
-
-
Ichinose, M.1
Fujimoto, T.2
Fukuchi, Y.3
-
27
-
-
57949112071
-
The efficacy of tiotropium administered via respimat soft mist inhaler or handiHaler in COPD patients
-
van Noord JA, Cornelissen PJ, Aumann JL, Platz J, Mueller A, et al. (2009) The efficacy of tiotropium administered via Respimat Soft Mist Inhaler or HandiHaler in COPD patients. Respir Med 103: 22-29.
-
(2009)
Respir Med
, vol.103
, pp. 22-29
-
-
Van Noord, J.A.1
Cornelissen, P.J.2
Aumann, J.L.3
Platz, J.4
Mueller, A.5
-
28
-
-
77952118055
-
-
emc+ website. Accessed 9 June 2013
-
Spiriva RESPIMAT. Summary of Product Characteristics (2010) emc+ website. Available: http://www.medicines.org.uk/EMC/medicine/20134/SPC/Spiriva+Respimat+2.5+micrograms+solution+for+inhalation/. Accessed 9 June 2013.
-
(2010)
Summary of Product Characteristics
-
-
Spiriva R.E.S.P.I.M.A.T.1
-
29
-
-
84858234304
-
Long-term inhaled dry powder mannitol in cystic fibrosis: An international randomized study
-
Aitken ML, Bellon G, De BK, Flume PA, Fox HG, et al. (2012) Long-term inhaled dry powder mannitol in cystic fibrosis: an international randomized study. Am J Respir Crit Care Med 185: 645-652.
-
(2012)
Am J Respir Crit Care Med
, vol.185
, pp. 645-652
-
-
Aitken, M.L.1
Bellon, G.2
De, B.K.3
Flume, P.A.4
Fox, H.G.5
-
30
-
-
84878360064
-
Pooled analysis of two large randomised phase III inhaled mannitol studies in cystic fibrosis
-
Bilton D, Bellon G, Charlton B, Cooper P, De BK, et al. (2013) Pooled analysis of two large randomised phase III inhaled mannitol studies in cystic fibrosis. J Cyst Fibros 12: 367-376.
-
(2013)
J Cyst Fibros
, vol.12
, pp. 367-376
-
-
Bilton, D.1
Bellon, G.2
Charlton, B.3
Cooper, P.4
De, B.K.5
-
31
-
-
30944466084
-
A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis
-
Elkins MR, Robinson M, Rose BR, Harbour C, Moriarty CP, et al. (2006) A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. N Engl J Med 354: 229-240.
-
(2006)
N Engl J Med
, vol.354
, pp. 229-240
-
-
Elkins, M.R.1
Robinson, M.2
Rose, B.R.3
Harbour, C.4
Moriarty, C.P.5
-
32
-
-
84880876390
-
Inhaled tobramycin effectively reduces FEV1 decline in cystic fibrosis. An instrumental variables analysis
-
Vandyke RD, McPhail GL, Huang B, Fenchel MC, Amin RS, et al. (2013) Inhaled tobramycin effectively reduces FEV1 decline in cystic fibrosis. An instrumental variables analysis. Ann Am Thorac Soc 10: 205-212.
-
(2013)
Ann Am Thorac Soc
, vol.10
, pp. 205-212
-
-
Vandyke, R.D.1
McPhail, G.L.2
Huang, B.3
Fenchel, M.C.4
Amin, R.S.5
-
33
-
-
80052689527
-
Health-related quality of life in cystic fibrosis
-
Royce FH, Carl JC (2011) Health-related quality of life in cystic fibrosis. Curr Opin Pediatr 23: 535-540.
-
(2011)
Curr Opin Pediatr
, vol.23
, pp. 535-540
-
-
Royce, F.H.1
Carl, J.C.2
-
34
-
-
66849121732
-
New aerosol delivery devices for cystic fibrosis
-
Kesser KC, Geller DE (2009) New aerosol delivery devices for cystic fibrosis. Respir Care 54: 754-767.
-
(2009)
Respir Care
, vol.54
, pp. 754-767
-
-
Kesser, K.C.1
Geller, D.E.2
|