-
1
-
-
84875829440
-
Cystic fibrosis pulmonary guidelines. Chronic medications for maintenance of lung health
-
Mogayzel PJ, Jr., Naureckas ET, Robinson KA, Mueller G, Hadjiliadis D, Hoag JB, Lubsch L, Hazle L, Sabadosa K, Marshall B, et al., Cystic fibrosis pulmonary guidelines. Chronic medications for maintenance of lung health. Am J Respir Crit Care Med 2013; 187: 680-689.
-
(2013)
Am J Respir Crit Care Med
, vol.187
, pp. 680-689
-
-
Mogayzel, P.J.1
Naureckas, E.T.2
Robinson, K.A.3
Mueller, G.4
Hadjiliadis, D.5
Hoag, J.B.6
Lubsch, L.7
Hazle, L.8
Sabadosa, K.9
Marshall, B.10
-
2
-
-
0029921953
-
Effects of 12-week administration of dornase alfa in patients with advanced cystic fibrosis lung disease. Pulmozyme Study Group
-
McCoy K, Hamilton S, Johnson C,. Effects of 12-week administration of dornase alfa in patients with advanced cystic fibrosis lung disease. Pulmozyme Study Group. Chest 1996; 110: 889-895.
-
(1996)
Chest
, vol.110
, pp. 889-895
-
-
McCoy, K.1
Hamilton, S.2
Johnson, C.3
-
3
-
-
0035666058
-
A two-year randomized, placebo-controlled trial of dornase alfa in young patients with cystic fibrosis with mild lung function abnormalities
-
Pulmozyme Early Intervention Trial Study G
-
Quan JM, Tiddens HA, Sy JP, McKenzie SG, Montgomery MD, Robinson PJ, Wohl ME, Konstan MW, Pulmozyme Early Intervention Trial Study G. 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
McKenzie, S.G.4
Montgomery, M.D.5
Robinson, P.J.6
Wohl, M.E.7
Konstan, M.W.8
-
4
-
-
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 HJ, Borowitz DS, Christiansen DH, Morris EM, Nash ML, Ramsey BW, Rosenstein BJ, Smith AL, Wohl ME,. 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
Morris, E.M.4
Nash, M.L.5
Ramsey, B.W.6
Rosenstein, B.J.7
Smith, A.L.8
Wohl, M.E.9
-
5
-
-
79955909454
-
Investigators, Coordinators of Epidemiologic Study of Cystic F. Clinical use of dornase alpha is associated with a slower rate of FEV1 decline in cystic fibrosis
-
Konstan MW, Wagener JS, Pasta DJ, Millar SJ, Jacobs JR, Yegin A, Morgan WJ, Scientific Advisory G,. Investigators, Coordinators of Epidemiologic Study of Cystic F. Clinical use of dornase alpha is associated with a slower rate of FEV1 decline in cystic fibrosis. Pediatr Pulmonol 2011; 46: 545-553.
-
(2011)
Pediatr Pulmonol
, vol.46
, pp. 545-553
-
-
Konstan, M.W.1
Wagener, J.S.2
Pasta, D.J.3
Millar, S.J.4
Jacobs, J.R.5
Yegin, A.6
Morgan, W.J.7
Scientific Advisory, G.8
-
6
-
-
84155165377
-
Reduced mortality in cystic fibrosis patients treated with tobramycin inhalation solution
-
Sawicki GS, Signorovitch JE, Zhang J, Latremouille-Viau D, von Wartburg M, Wu EQ, Shi L,. Reduced mortality in cystic fibrosis patients treated with tobramycin inhalation solution. Pediatr Pulmonol 2012; 47: 44-52.
-
(2012)
Pediatr Pulmonol
, vol.47
, pp. 44-52
-
-
Sawicki, G.S.1
Signorovitch, J.E.2
Zhang, J.3
Latremouille-Viau, D.4
Von Wartburg, M.5
Wu, E.Q.6
Shi, L.7
-
7
-
-
84902328031
-
Sinonasal inhalation of dornase alfa administered by vibrating aerosol to cystic fibrosis patients: A double-blind placebo-controlled cross-over trial
-
Mainz JG, Schien C, Schiller I, Schadlich K, Koitschev A, Koitschev C, Riethmuller J, Graepler-Mainka U, Wiedemann B, Beck JF,. Sinonasal inhalation of dornase alfa administered by vibrating aerosol to cystic fibrosis patients: a double-blind placebo-controlled cross-over trial. J Cyst Fibros 2014; 13: 461-470.
-
(2014)
J Cyst Fibros
, vol.13
, pp. 461-470
-
-
Mainz, J.G.1
Schien, C.2
Schiller, I.3
Schadlich, K.4
Koitschev, A.5
Koitschev, C.6
Riethmuller, J.7
Graepler-Mainka, U.8
Wiedemann, B.9
Beck, J.F.10
-
8
-
-
84891709285
-
Timing of dornase alfa inhalation for cystic fibrosis
-
Dentice R, Elkins M,. Timing of dornase alfa inhalation for cystic fibrosis. Cochrane Database Syst Rev 2013; 6: CD007923.
-
(2013)
Cochrane Database Syst Rev
, vol.6
, pp. CD007923
-
-
Dentice, R.1
Elkins, M.2
-
9
-
-
0029916071
-
Effect of hypertonic saline, amiloride, and cough on mucociliary clearance in patients with cystic fibrosis
-
Robinson M, Regnis JA, Bailey DL, King M, Bautovich GJ, Bye PT,. Effect of hypertonic saline, amiloride, and cough on mucociliary clearance in patients with cystic fibrosis. Am J Respir Crit Care Med 1996; 153: 1503-1509.
-
(1996)
Am J Respir Crit Care Med
, vol.153
, pp. 1503-1509
-
-
Robinson, M.1
Regnis, J.A.2
Bailey, D.L.3
King, M.4
Bautovich, G.J.5
Bye, P.T.6
-
10
-
-
0030784262
-
Effect of increasing doses of hypertonic saline on mucociliary clearance in patients with cystic fibrosis
-
Robinson M, Hemming AL, Regnis JA, Wong AG, Bailey DL, Bautovich GJ, King M, Bye PT,. Effect of increasing doses of hypertonic saline on mucociliary clearance in patients with cystic fibrosis. Thorax 1997; 52: 900-903.
-
(1997)
Thorax
, vol.52
, pp. 900-903
-
-
Robinson, M.1
Hemming, A.L.2
Regnis, J.A.3
Wong, A.G.4
Bailey, D.L.5
Bautovich, G.J.6
King, M.7
Bye, P.T.8
-
11
-
-
30944452384
-
Mucus clearance and lung function in cystic fibrosis with hypertonic saline
-
Donaldson SH, Bennett WD, Zeman KL, Knowles MR, Tarran R, Boucher RC,. Mucus clearance and lung function in cystic fibrosis with hypertonic saline. N Engl J Med 2006; 354: 241-250.
-
(2006)
N Engl J Med
, vol.354
, pp. 241-250
-
-
Donaldson, S.H.1
Bennett, W.D.2
Zeman, K.L.3
Knowles, M.R.4
Tarran, R.5
Boucher, R.C.6
-
12
-
-
30944466084
-
A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis
-
National Hypertonic Saline in Cystic Fibrosis Study G
-
Elkins MR, Robinson M, Rose BR, Harbour C, Moriarty CP, Marks GB, Belousova EG, Xuan W, Bye PT, National Hypertonic Saline in Cystic Fibrosis Study G. 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
Harbour, C.4
Moriarty, C.P.5
Marks, G.B.6
Belousova, E.G.7
Xuan, W.8
Bye, P.T.9
-
13
-
-
84901048948
-
Sustained effect of hypertonic saline on mucociliary clearance in CF children with mild lung disease
-
Donaldson SH, Samulski D, LaFave C, Wu J, Zeman K, Salazar C, Bennett WD, Davis SD,. Sustained effect of hypertonic saline on mucociliary clearance in CF children with mild lung disease. Pediatr Pulmonol 2013; 48: 210.
-
(2013)
Pediatr Pulmonol
, vol.48
, pp. 210
-
-
Donaldson, S.H.1
Samulski, D.2
LaFave, C.3
Wu, J.4
Zeman, K.5
Salazar, C.6
Bennett, W.D.7
Davis, S.D.8
-
14
-
-
77951988740
-
Hypertonic saline improves the LCI in paediatric patients with CF with normal lung function
-
Amin R, Subbarao P, Jabar A, Balkovec S, Jensen R, Kerrigan S, Gustafsson P, Ratjen F,. Hypertonic saline improves the LCI in paediatric patients with CF with normal lung function. Thorax 2010; 65: 379-383.
-
(2010)
Thorax
, vol.65
, pp. 379-383
-
-
Amin, R.1
Subbarao, P.2
Jabar, A.3
Balkovec, S.4
Jensen, R.5
Kerrigan, S.6
Gustafsson, P.7
Ratjen, F.8
-
15
-
-
57349158832
-
Safety and tolerability of inhaled hypertonic saline in young children with cystic fibrosis
-
Dellon EP, Donaldson SH, Johnson R, Davis SD,. Safety and tolerability of inhaled hypertonic saline in young children with cystic fibrosis. Pediatr Pulmonol 2008; 43: 1100-1106.
-
(2008)
Pediatr Pulmonol
, vol.43
, pp. 1100-1106
-
-
Dellon, E.P.1
Donaldson, S.H.2
Johnson, R.3
Davis, S.D.4
-
16
-
-
34247880282
-
Pilot study of safety and tolerability of inhaled hypertonic saline in infants with cystic fibrosis
-
Subbarao P, Balkovec S, Solomon M, Ratjen F,. Pilot study of safety and tolerability of inhaled hypertonic saline in infants with cystic fibrosis. Pediatr Pulmonol 2007; 42: 471-476.
-
(2007)
Pediatr Pulmonol
, vol.42
, pp. 471-476
-
-
Subbarao, P.1
Balkovec, S.2
Solomon, M.3
Ratjen, F.4
-
17
-
-
79959828264
-
Inhaled hypertonic saline in infants and toddlers with cystic fibrosis: Short-term tolerability, adherence, and safety
-
Rosenfeld M, Davis S, Brumback L, Daniel S, Rowbotham R, Johnson R, McNamara S, Jensen R, Barlow C, Ratjen F,. Inhaled hypertonic saline in infants and toddlers with cystic fibrosis: short-term tolerability, adherence, and safety. Pediatr Pulmonol 2011; 46: 666-671.
-
(2011)
Pediatr Pulmonol
, vol.46
, pp. 666-671
-
-
Rosenfeld, M.1
Davis, S.2
Brumback, L.3
Daniel, S.4
Rowbotham, R.5
Johnson, R.6
McNamara, S.7
Jensen, R.8
Barlow, C.9
Ratjen, F.10
-
18
-
-
84861892411
-
Inhaled hypertonic saline in infants and children younger than 6 years with cystic fibrosis: The ISIS randomized controlled trial
-
Rosenfeld M, Ratjen F, Brumback L, Daniel S, Rowbotham R, McNamara S, Johnson R, Kronmal R, Davis SD, Group IS,. Inhaled hypertonic saline in infants and children younger than 6 years with cystic fibrosis: the ISIS randomized controlled trial. JAMA 2012; 307: 2269-2277.
-
(2012)
JAMA
, vol.307
, pp. 2269-2277
-
-
Rosenfeld, M.1
Ratjen, F.2
Brumback, L.3
Daniel, S.4
Rowbotham, R.5
McNamara, S.6
Johnson, R.7
Kronmal, R.8
Davis, S.D.9
Group, I.S.10
-
19
-
-
84882662774
-
Lung clearance index as an outcome measure for clinical trials in young children with cystic fibrosis. A pilot study using inhaled hypertonic saline
-
Subbarao P, Stanojevic S, Brown M, Jensen R, Rosenfeld M, Davis S, Brumback L, Gustafsson P, Ratjen F,. Lung clearance index as an outcome measure for clinical trials in young children with cystic fibrosis. A pilot study using inhaled hypertonic saline. Am J Respir Crit Care Med 2013; 188: 456-460.
-
(2013)
Am J Respir Crit Care Med
, vol.188
, pp. 456-460
-
-
Subbarao, P.1
Stanojevic, S.2
Brown, M.3
Jensen, R.4
Rosenfeld, M.5
Davis, S.6
Brumback, L.7
Gustafsson, P.8
Ratjen, F.9
-
20
-
-
42949178050
-
Effect of increasing doses of mannitol on mucus clearance in patients with bronchiectasis
-
Daviskas E, Anderson SD, Eberl S, Young IH,. Effect of increasing doses of mannitol on mucus clearance in patients with bronchiectasis. Eur Respir J 2008; 31: 765-772.
-
(2008)
Eur Respir J
, vol.31
, pp. 765-772
-
-
Daviskas, E.1
Anderson, S.D.2
Eberl, S.3
Young, I.H.4
-
21
-
-
84878360064
-
Pooled analysis of two large randomised phase III inhaled mannitol studies in cystic fibrosis
-
Bilton D, Bellon G, Charlton B, Cooper P, De Boeck K, Flume PA, Fox HG, Gallagher CG, Geller DE, Haarman EG, et al., Pooled analysis of two large randomised phase III inhaled mannitol studies in cystic fibrosis. J Cyst Fibros 2013; 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 Boeck, K.5
Flume, P.A.6
Fox, H.G.7
Gallagher, C.G.8
Geller, D.E.9
Haarman, E.G.10
-
22
-
-
44649166466
-
Inhaled mannitol improves lung function in cystic fibrosis
-
Jaques A, Daviskas E, Turton JA, McKay K, Cooper P, Stirling RG, Robertson CF, Bye PT, Lesouef PN, Shadbolt B, 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
McKay, K.4
Cooper, P.5
Stirling, R.G.6
Robertson, C.F.7
Bye, P.T.8
Lesouef, P.N.9
Shadbolt, B.10
-
23
-
-
84858234304
-
Long-term inhaled dry powder mannitol in cystic fibrosis: An international randomized study
-
Aitken ML, Bellon G, De Boeck K, Flume PA, Fox HG, Geller DE, Haarman EG, Hebestreit HU, Lapey A, Schou IM, et al., Long-term inhaled dry powder mannitol in cystic fibrosis: an international randomized study. Am J Respir Crit Care Med 2012; 185: 645-652.
-
(2012)
Am J Respir Crit Care Med
, vol.185
, pp. 645-652
-
-
Aitken, M.L.1
Bellon, G.2
De Boeck, K.3
Flume, P.A.4
Fox, H.G.5
Geller, D.E.6
Haarman, E.G.7
Hebestreit, H.U.8
Lapey, A.9
Schou, I.M.10
-
24
-
-
80355127141
-
Inhaled dry powder mannitol in cystic fibrosis: An efficacy and safety study
-
Investigators C.F.S.
-
Bilton D, Robinson P, Cooper P, Gallagher CG, Kolbe J, Fox H, Jaques A, Charlton B, Investigators CFS,. Inhaled dry powder mannitol in cystic fibrosis: an efficacy and safety study. Eur Respir J 2011; 38: 1071-1080.
-
(2011)
Eur Respir J
, vol.38
, pp. 1071-1080
-
-
Bilton, D.1
Robinson, P.2
Cooper, P.3
Gallagher, C.G.4
Kolbe, J.5
Fox, H.6
Jaques, A.7
Charlton, B.8
-
25
-
-
84884282606
-
ENaC inhibitors and airway re-hydration in cystic fibrosis: State of the art
-
Althaus M,. ENaC inhibitors and airway re-hydration in cystic fibrosis: state of the art. Curr Mol Pharmacol 2013; 6: 3-12.
-
(2013)
Curr Mol Pharmacol
, vol.6
, pp. 3-12
-
-
Althaus, M.1
-
26
-
-
84929175850
-
NVP-QB E170: An inhaled ENaC blocker with a reduced potential to induce hyperkalaemia
-
Coote KJ, Paisley D, Czarnecki S, Tweed M, Watson H, Young A, Sugar R, Vyas M, Smith NJ, Baettig U, et al., NVP-QB E170: an inhaled ENaC blocker with a reduced potential to induce hyperkalaemia. Br J Pharmacol 2015; 172: 2814-2826.
-
(2015)
Br J Pharmacol
, vol.172
, pp. 2814-2826
-
-
Coote, K.J.1
Paisley, D.2
Czarnecki, S.3
Tweed, M.4
Watson, H.5
Young, A.6
Sugar, R.7
Vyas, M.8
Smith, N.J.9
Baettig, U.10
-
27
-
-
84901721726
-
Acute hyperkalemia associated with inhalation of a potent ENaC antagonist: Phase 1 trial of GS-9411
-
O'Riordan TG, Donn KH, Hodsman P, Ansede JH, Newcomb T, Lewis SA, Flitter WD, White VS, Johnson MR, Montgomery AB, et al., Acute hyperkalemia associated with inhalation of a potent ENaC antagonist: phase 1 trial of GS-9411. J Aerosol Med Pulm Drug Deliv 2014; 27: 200-208.
-
(2014)
J Aerosol Med Pulm Drug Deliv
, vol.27
, pp. 200-208
-
-
O'Riordan, T.G.1
Donn, K.H.2
Hodsman, P.3
Ansede, J.H.4
Newcomb, T.5
Lewis, S.A.6
Flitter, W.D.7
White, V.S.8
Johnson, M.R.9
Montgomery, A.B.10
-
28
-
-
0033531143
-
Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic Fibrosis Inhaled Tobramycin Study Group
-
Ramsey BW, Pepe MS, Quan JM, Otto KL, Montgomery AB, Williams-Warren J, Vasiljev KM, Borowitz D, Bowman CM, Marshall BC, et al., Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic Fibrosis Inhaled Tobramycin Study Group. 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
Otto, K.L.4
Montgomery, A.B.5
Williams-Warren, J.6
Vasiljev, K.M.7
Borowitz, D.8
Bowman, C.M.9
Marshall, B.C.10
-
29
-
-
84898756200
-
Azithromycin may antagonize inhaled tobramycin when targeting Pseudomonas aeruginosa in cystic fibrosis
-
Nick JA, Moskowitz SM, Chmiel JF, Forssen AV, Kim SH, Saavedra MT, Saiman L, Taylor-Cousar JL, Nichols DP,. Azithromycin may antagonize inhaled tobramycin when targeting Pseudomonas aeruginosa in cystic fibrosis. Ann Am Thorac Soc 2014; 11: 342-350.
-
(2014)
Ann Am Thorac Soc
, vol.11
, pp. 342-350
-
-
Nick, J.A.1
Moskowitz, S.M.2
Chmiel, J.F.3
Forssen, A.V.4
Kim, S.H.5
Saavedra, M.T.6
Saiman, L.7
Taylor-Cousar, J.L.8
Nichols, D.P.9
-
30
-
-
84866172783
-
A network meta-analysis of the efficacy of inhaled antibiotics for chronic Pseudomonas infections in cystic fibrosis
-
Littlewood KJ, Higashi K, Jansen JP, Capkun-Niggli G, Balp MM, Doering G, Tiddens HA, Angyalosi G,. A network meta-analysis of the efficacy of inhaled antibiotics for chronic Pseudomonas infections in cystic fibrosis. J Cyst Fibros 2012; 11: 419-426.
-
(2012)
J Cyst Fibros
, vol.11
, pp. 419-426
-
-
Littlewood, K.J.1
Higashi, K.2
Jansen, J.P.3
Capkun-Niggli, G.4
Balp, M.M.5
Doering, G.6
Tiddens, H.A.7
Angyalosi, G.8
-
31
-
-
84892693489
-
Long-term efficacy and safety of aerosolized tobramycin 300 mg/4 ml in cystic fibrosis
-
Mazurek H, Chiron R, Kucerova T, Geidel C, Bolbas K, Chuchalin A, Blanco-Aparicio M, Santoro D, Varoli G, Zibellini M, et al., Long-term efficacy and safety of aerosolized tobramycin 300 mg/4 ml in cystic fibrosis. Pediatr Pulmonol 2014; 49: 1076-1089.
-
(2014)
Pediatr Pulmonol
, vol.49
, pp. 1076-1089
-
-
Mazurek, H.1
Chiron, R.2
Kucerova, T.3
Geidel, C.4
Bolbas, K.5
Chuchalin, A.6
Blanco-Aparicio, M.7
Santoro, D.8
Varoli, G.9
Zibellini, M.10
-
32
-
-
84895072308
-
Effectiveness of inhaled tobramycin in eradicating Pseudomonas aeruginosa in children with cystic fibrosis
-
Stanojevic S, Waters V, Mathew JL, Taylor L, Ratjen F,. Effectiveness of inhaled tobramycin in eradicating Pseudomonas aeruginosa in children with cystic fibrosis. J Cyst Fibros 2014; 13: 172-178.
-
(2014)
J Cyst Fibros
, vol.13
, pp. 172-178
-
-
Stanojevic, S.1
Waters, V.2
Mathew, J.L.3
Taylor, L.4
Ratjen, F.5
-
33
-
-
80052511405
-
Comparative efficacy and safety of 4 randomized regimens to treat early Pseudomonas aeruginosa infection in children with cystic fibrosis
-
Treggiari MM, Retsch-Bogart G, Mayer-Hamblett N, Khan U, Kulich M, Kronmal R, Williams J, Hiatt P, Gibson RL, Spencer T, et al., Comparative efficacy and safety of 4 randomized regimens to treat early Pseudomonas aeruginosa infection in children with cystic fibrosis. Arch Pediatr Adolesc Med 2011; 165: 847-856.
-
(2011)
Arch Pediatr Adolesc Med
, vol.165
, pp. 847-856
-
-
Treggiari, M.M.1
Retsch-Bogart, G.2
Mayer-Hamblett, N.3
Khan, U.4
Kulich, M.5
Kronmal, R.6
Williams, J.7
Hiatt, P.8
Gibson, R.L.9
Spencer, T.10
-
34
-
-
77950914953
-
Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: The ELITE trial
-
Ratjen F, Munck A, Kho P, Angyalosi G, Group ES,. Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: the ELITE trial. Thorax 2010; 65: 286-291.
-
(2010)
Thorax
, vol.65
, pp. 286-291
-
-
Ratjen, F.1
Munck, A.2
Kho, P.3
Angyalosi, G.4
Group, E.S.5
-
35
-
-
84900031485
-
Clinical use of tobramycin inhalation solution (TOBI(R)) shows sustained improvement in FEV1 in cystic fibrosis
-
Konstan MW, Wagener JS, Pasta DJ, Millar SJ, Morgan WJ,. Clinical use of tobramycin inhalation solution (TOBI(R)) shows sustained improvement in FEV1 in cystic fibrosis. Pediatr Pulmonol 2014; 49: 529-536.
-
(2014)
Pediatr Pulmonol
, vol.49
, pp. 529-536
-
-
Konstan, M.W.1
Wagener, J.S.2
Pasta, D.J.3
Millar, S.J.4
Morgan, W.J.5
-
36
-
-
80053377162
-
Tobramycin inhalation powder: A novel drug delivery system for treating chronic Pseudomonas aeruginosa infection in cystic fibrosis
-
Parkins MD, Elborn JS,. Tobramycin inhalation powder: a novel drug delivery system for treating chronic Pseudomonas aeruginosa infection in cystic fibrosis. Expert Rev Respir Med 2011; 5: 609-622.
-
(2011)
Expert Rev Respir Med
, vol.5
, pp. 609-622
-
-
Parkins, M.D.1
Elborn, J.S.2
-
37
-
-
79951840468
-
Tobramycin inhalation powder for P. Aeruginosa infection in cystic fibrosis: The EVOLVE trial
-
Konstan MW, Geller DE, Minic P, Brockhaus F, Zhang J, Angyalosi G,. Tobramycin inhalation powder for P. Aeruginosa infection in cystic fibrosis: the EVOLVE trial. Pediatr Pulmonol 2011; 46: 230-238.
-
(2011)
Pediatr Pulmonol
, vol.46
, pp. 230-238
-
-
Konstan, M.W.1
Geller, D.E.2
Minic, P.3
Brockhaus, F.4
Zhang, J.5
Angyalosi, G.6
-
38
-
-
84911956623
-
Inhaled versus nebulised tobramycin: A real world comparison in adult cystic fibrosis (CF)
-
Harrison MJ, McCarthy M, Fleming C, Hickey C, Shortt C, Eustace JA, Murphy DM, Plant BJ,. Inhaled versus nebulised tobramycin: a real world comparison in adult cystic fibrosis (CF). J Cyst Fibros 2014; 13: 692-698.
-
(2014)
J Cyst Fibros
, vol.13
, pp. 692-698
-
-
Harrison, M.J.1
McCarthy, M.2
Fleming, C.3
Hickey, C.4
Shortt, C.5
Eustace, J.A.6
Murphy, D.M.7
Plant, B.J.8
-
39
-
-
84888992940
-
Tobramycin inhalation powder in cystic fibrosis patients: Response by age group
-
Geller DE, Nasr SZ, Piggott S, He E, Angyalosi G, Higgins M,. Tobramycin inhalation powder in cystic fibrosis patients: response by age group. Respir Care 2014; 59: 388-398.
-
(2014)
Respir Care
, vol.59
, pp. 388-398
-
-
Geller, D.E.1
Nasr, S.Z.2
Piggott, S.3
He, E.4
Angyalosi, G.5
Higgins, M.6
-
40
-
-
78651412529
-
Safety, efficacy and convenience of tobramycin inhalation powder in cystic fibrosis patients: The EAGER trial
-
Konstan MW, Flume PA, Kappler M, Chiron R, Higgins M, Brockhaus F, Zhang J, Angyalosi G, He E, Geller DE,. Safety, efficacy and convenience of tobramycin inhalation powder in cystic fibrosis patients: The EAGER trial. J Cyst Fibros 2011; 10: 54-61.
-
(2011)
J Cyst Fibros
, vol.10
, pp. 54-61
-
-
Konstan, M.W.1
Flume, P.A.2
Kappler, M.3
Chiron, R.4
Higgins, M.5
Brockhaus, F.6
Zhang, J.7
Angyalosi, G.8
He, E.9
Geller, D.E.10
-
41
-
-
55549137086
-
Inhaled aztreonam lysine for chronic airway Pseudomonas aeruginosa in cystic fibrosis
-
McCoy KS, Quittner AL, Oermann CM, Gibson RL, Retsch-Bogart GZ, Montgomery AB,. 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
-
42
-
-
78449294500
-
An 18-month study of the safety and efficacy of repeated courses of inhaled aztreonam lysine in cystic fibrosis
-
Oermann CM, Retsch-Bogart GZ, Quittner AL, Gibson RL, McCoy KS, Montgomery AB, Cooper PJ,. An 18-month study of the safety and efficacy of repeated courses of inhaled aztreonam lysine in cystic fibrosis. Pediatr Pulmonol 2010; 45: 1121-1134.
-
(2010)
Pediatr Pulmonol
, vol.45
, pp. 1121-1134
-
-
Oermann, C.M.1
Retsch-Bogart, G.Z.2
Quittner, A.L.3
Gibson, R.L.4
McCoy, K.S.5
Montgomery, A.B.6
Cooper, P.J.7
-
43
-
-
84918771958
-
Open label study of inhaled aztreonam for Pseudomonas eradication in children with cystic fibrosis: The ALPINE study
-
H GMA, investigators As
-
Tiddens HA, De Boeck K, Clancy JP, Fayon M, H GMA, Bresnik M, Derchak A, Lewis SA, Oermann CM, investigators As. Open label study of inhaled aztreonam for Pseudomonas eradication in children with cystic fibrosis: the ALPINE study. J Cyst Fibros 2015; 14: 111-119.
-
(2015)
J Cyst Fibros
, vol.14
, pp. 111-119
-
-
Tiddens, H.A.1
De Boeck, K.2
Clancy, J.P.3
Fayon, M.4
Bresnik, M.5
Derchak, A.6
Lewis, S.A.7
Oermann, C.M.8
-
44
-
-
79958295843
-
Aztreonam for inhalation solution (AZLI) in patients with cystic fibrosis, mild lung impairment, and P. Aeruginosa
-
Wainwright CE, Quittner AL, Geller DE, Nakamura C, Wooldridge JL, Gibson RL, Lewis S, Montgomery AB,. Aztreonam for inhalation solution (AZLI) in patients with cystic fibrosis, mild lung impairment, and P. Aeruginosa. J Cyst Fibros 2011; 10: 234-242.
-
(2011)
J Cyst Fibros
, vol.10
, pp. 234-242
-
-
Wainwright, C.E.1
Quittner, A.L.2
Geller, D.E.3
Nakamura, C.4
Wooldridge, J.L.5
Gibson, R.L.6
Lewis, S.7
Montgomery, A.B.8
-
45
-
-
84875842391
-
Inhaled aztreonam lysine vs. Inhaled tobramycin in cystic fibrosis: A comparative efficacy trial
-
Assael BM, Pressler T, Bilton D, Fayon M, Fischer R, Chiron R, LaRosa M, Knoop C, McElvaney N, Lewis SA, et al., Inhaled aztreonam lysine vs. inhaled tobramycin in cystic fibrosis: a comparative efficacy trial. J Cyst Fibros 2013; 12: 130-140.
-
(2013)
J Cyst Fibros
, vol.12
, pp. 130-140
-
-
Assael, B.M.1
Pressler, T.2
Bilton, D.3
Fayon, M.4
Fischer, R.5
Chiron, R.6
LaRosa, M.7
Knoop, C.8
McElvaney, N.9
Lewis, S.A.10
-
46
-
-
80052892852
-
Pseudomonas aeruginosa antibiotic susceptibility during long-term use of aztreonam for inhalation solution (AZLI)
-
Oermann CM, McCoy KS, Retsch-Bogart GZ, Gibson RL, McKevitt M, Montgomery AB,. Pseudomonas aeruginosa antibiotic susceptibility during long-term use of aztreonam for inhalation solution (AZLI). J Antimicrob Chemother 2011; 66: 2398-2404.
-
(2011)
J Antimicrob Chemother
, vol.66
, pp. 2398-2404
-
-
Oermann, C.M.1
McCoy, K.S.2
Retsch-Bogart, G.Z.3
Gibson, R.L.4
McKevitt, M.5
Montgomery, A.B.6
-
47
-
-
84870742117
-
Comparison of two treatment regimens for eradication of Pseudomonas aeruginosa infection in children with cystic fibrosis
-
Proesmans M, Vermeulen F, Boulanger L, Verhaegen J, De Boeck K,. Comparison of two treatment regimens for eradication of Pseudomonas aeruginosa infection in children with cystic fibrosis. J Cyst Fibros 2013; 12: 29-34.
-
(2013)
J Cyst Fibros
, vol.12
, pp. 29-34
-
-
Proesmans, M.1
Vermeulen, F.2
Boulanger, L.3
Verhaegen, J.4
De Boeck, K.5
-
48
-
-
84875215401
-
Efficacy and convenience of colistimethate sodium dry powder for inhalation (Colobreathe DPI) in patients with cystic fibrosis: A randomised study
-
Schuster A, Haliburn C, Doring G, Goldman MH, Freedom Study,. Efficacy and convenience of colistimethate sodium dry powder for inhalation (Colobreathe DPI) in patients with cystic fibrosis: a randomised study. Thorax 2013; 68: 344-350.
-
(2013)
Thorax
, vol.68
, pp. 344-350
-
-
Schuster, A.1
Haliburn, C.2
Doring, G.3
Goldman, M.H.4
Freedom, S.5
-
49
-
-
84866061431
-
Italian Group for PaEiCF. Early antibiotic treatment for Pseudomonas aeruginosa eradication in patients with cystic fibrosis: A randomised multicentre study comparing two different protocols
-
Taccetti G, Bianchini E, Cariani L, Buzzetti R, Costantini D, Trevisan F, Zavataro L, Campana S,. Italian Group for PaEiCF. Early antibiotic treatment for Pseudomonas aeruginosa eradication in patients with cystic fibrosis: a randomised multicentre study comparing two different protocols. Thorax 2012; 67: 853-859.
-
(2012)
Thorax
, vol.67
, pp. 853-859
-
-
Taccetti, G.1
Bianchini, E.2
Cariani, L.3
Buzzetti, R.4
Costantini, D.5
Trevisan, F.6
Zavataro, L.7
Campana, S.8
-
50
-
-
84937628442
-
A phase 3, open-label, randomized trial to evaluate the safety and efficacy of levofloxacin inhalation solution (APT -1026) versus tobramycin inhalation solution in stable cystic fibrosis patients
-
Stuart Elborn J, Geller DE, Conrad D, Aaron SD, Smyth AR, Fischer R, Kerem E, Bell SC, Loutit JS, Dudley MN, et al., A phase 3, open-label, randomized trial to evaluate the safety and efficacy of levofloxacin inhalation solution (APT -1026) versus tobramycin inhalation solution in stable cystic fibrosis patients. J Cyst Fibros 2015; 14: 507-514.
-
(2015)
J Cyst Fibros
, vol.14
, pp. 507-514
-
-
Stuart Elborn, J.1
Geller, D.E.2
Conrad, D.3
Aaron, S.D.4
Smyth, A.R.5
Fischer, R.6
Kerem, E.7
Bell, S.C.8
Loutit, J.S.9
Dudley, M.N.10
-
51
-
-
79957942626
-
Mpex 204 Study G. Levofloxacin inhalation solution (MP-376) in patients with cystic fibrosis with Pseudomonas aeruginosa
-
Geller DE, Flume PA, Staab D, Fischer R, Loutit JS, Conrad DJ,. Mpex 204 Study G. Levofloxacin inhalation solution (MP-376) in patients with cystic fibrosis with Pseudomonas aeruginosa. Am J Respir Crit Care Med 2011; 183: 1510-1516.
-
(2011)
Am J Respir Crit Care Med
, vol.183
, pp. 1510-1516
-
-
Geller, D.E.1
Flume, P.A.2
Staab, D.3
Fischer, R.4
Loutit, J.S.5
Conrad, D.J.6
-
52
-
-
84920989635
-
Levofloxacin inhalation solution for the treatment of chronic Pseudomonas aeruginosa infection among patients with cystic fibrosis
-
Stockmann C, Hillyard B, Ampofo K, Spigarelli MG, Sherwin CM,. Levofloxacin inhalation solution for the treatment of chronic Pseudomonas aeruginosa infection among patients with cystic fibrosis. Expert Rev Respir Med 2015; 9: 13-22.
-
(2015)
Expert Rev Respir Med
, vol.9
, pp. 13-22
-
-
Stockmann, C.1
Hillyard, B.2
Ampofo, K.3
Spigarelli, M.G.4
Sherwin, C.M.5
-
53
-
-
84893507930
-
Inhaled amikacin for treatment of refractory pulmonary nontuberculous mycobacterial disease
-
Olivier KN, Shaw PA, Glaser TS, Bhattacharyya D, Fleshner M, Brewer CC, Zalewski CK, Folio LR, Siegelman JR, Shallom S, et al., Inhaled amikacin for treatment of refractory pulmonary nontuberculous mycobacterial disease. Ann Am Thorac Soc 2014; 11: 30-35.
-
(2014)
Ann Am Thorac Soc
, vol.11
, pp. 30-35
-
-
Olivier, K.N.1
Shaw, P.A.2
Glaser, T.S.3
Bhattacharyya, D.4
Fleshner, M.5
Brewer, C.C.6
Zalewski, C.K.7
Folio, L.R.8
Siegelman, J.R.9
Shallom, S.10
-
54
-
-
84881542878
-
Phase II studies of nebulised Arikace in CF patients with Pseudomonas aeruginosa infection
-
Clancy JP, Dupont L, Konstan MW, Billings J, Fustik S, Goss CH, Lymp J, Minic P, Quittner AL, Rubenstein RC, et al., Phase II studies of nebulised Arikace in CF patients with Pseudomonas aeruginosa infection. Thorax 2013; 68: 818-825.
-
(2013)
Thorax
, vol.68
, pp. 818-825
-
-
Clancy, J.P.1
Dupont, L.2
Konstan, M.W.3
Billings, J.4
Fustik, S.5
Goss, C.H.6
Lymp, J.7
Minic, P.8
Quittner, A.L.9
Rubenstein, R.C.10
-
55
-
-
84880819676
-
Resistance development of cystic fibrosis respiratory pathogens when exposed to fosfomycin and tobramycin alone and in combination under aerobic and anaerobic conditions
-
McCaughey G, Diamond P, Elborn JS, McKevitt M, Tunney MM,. Resistance development of cystic fibrosis respiratory pathogens when exposed to fosfomycin and tobramycin alone and in combination under aerobic and anaerobic conditions. PLoS ONE 2013; 8: e69763.
-
(2013)
PLoS ONE
, vol.8
, pp. e69763
-
-
McCaughey, G.1
Diamond, P.2
Elborn, J.S.3
McKevitt, M.4
Tunney, M.M.5
-
56
-
-
84856010859
-
Fosfomycin/tobramycin for inhalation in patients with cystic fibrosis with pseudomonas airway infection
-
Trapnell BC, McColley SA, Kissner DG, Rolfe MW, Rosen JM, McKevitt M, Moorehead L, Montgomery AB, Geller DE, Phase FTISG,. Fosfomycin/tobramycin for inhalation in patients with cystic fibrosis with pseudomonas airway infection. Am J Respir Crit Care Med 2012; 185: 171-178.
-
(2012)
Am J Respir Crit Care Med
, vol.185
, pp. 171-178
-
-
Trapnell, B.C.1
McColley, S.A.2
Kissner, D.G.3
Rolfe, M.W.4
Rosen, J.M.5
McKevitt, M.6
Moorehead, L.7
Montgomery, A.B.8
Geller, D.E.9
Phase, F.10
-
57
-
-
74049117459
-
Aerosolized vancomycin for the treatment of MRSA after lung transplantation
-
Hayes D, Jr., Murphy BS, Mullett TW, Feola DJ,. Aerosolized vancomycin for the treatment of MRSA after lung transplantation. Respirology 2010; 15: 184-186.
-
(2010)
Respirology
, vol.15
, pp. 184-186
-
-
Hayes, D.1
Murphy, B.S.2
Mullett, T.W.3
Feola, D.J.4
-
58
-
-
0031751584
-
Aerosolized vancomycin for the treatment of methicillin-resistant Staphylococcus aureus infection in cystic fibrosis
-
Maiz L, Canton R, Mir N, Baquero F, Escobar H,. Aerosolized vancomycin for the treatment of methicillin-resistant Staphylococcus aureus infection in cystic fibrosis. Pediatr Pulmonol 1998; 26: 287-289.
-
(1998)
Pediatr Pulmonol
, vol.26
, pp. 287-289
-
-
Maiz, L.1
Canton, R.2
Mir, N.3
Baquero, F.4
Escobar, H.5
-
59
-
-
84902975826
-
Eradication strategy for persistent methicillin-resistant Staphylococcus aureus infection in individuals with cystic fibrosis - The PMEP trial: Study protocol for a randomized controlled trial
-
Jennings MT, Boyle MP, Weaver D, Callahan KA, Dasenbrook EC,. Eradication strategy for persistent methicillin-resistant Staphylococcus aureus infection in individuals with cystic fibrosis - The PMEP trial: study protocol for a randomized controlled trial. Trials 2014; 15: 223.
-
(2014)
Trials
, vol.15
, pp. 223
-
-
Jennings, M.T.1
Boyle, M.P.2
Weaver, D.3
Callahan, K.A.4
Dasenbrook, E.C.5
-
60
-
-
0141816759
-
Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: A randomized controlled trial
-
Saiman L, Marshall BC, Mayer-Hamblett N, Burns JL, Quittner AL, Cibene DA, Coquillette S, Fieberg AY, Accurso FJ, Campbell PW, III, 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
Burns, J.L.4
Quittner, A.L.5
Cibene, D.A.6
Coquillette, S.7
Fieberg, A.Y.8
Accurso, F.J.9
Campbell, P.W.10
-
61
-
-
79955484840
-
Macrolide antibiotics broadly and distinctively inhibit cytokine and chemokine production by COPD sputum cells in vitro
-
Marjanovic N, Bosnar M, Michielin F, Wille DR, Anic-Milic T, Culic O, Popovic-Grle S, Bogdan M, Parnham MJ, Erakovic Haber V,. Macrolide antibiotics broadly and distinctively inhibit cytokine and chemokine production by COPD sputum cells in vitro. Pharmacol Res 2011; 63: 389-397.
-
(2011)
Pharmacol Res
, vol.63
, pp. 389-397
-
-
Marjanovic, N.1
Bosnar, M.2
Michielin, F.3
Wille, D.R.4
Anic-Milic, T.5
Culic, O.6
Popovic-Grle, S.7
Bogdan, M.8
Parnham, M.J.9
Erakovic Haber, V.10
-
62
-
-
10844296436
-
Azithromycin retards Pseudomonas aeruginosa biofilm formation
-
Gillis RJ, Iglewski BH,. Azithromycin retards Pseudomonas aeruginosa biofilm formation. J Clin Microbiol 2004; 42: 5842-5845.
-
(2004)
J Clin Microbiol
, vol.42
, pp. 5842-5845
-
-
Gillis, R.J.1
Iglewski, B.H.2
-
63
-
-
84922206485
-
Novel antiviral properties of azithromycin in cystic fibrosis airway epithelial cells
-
Schogler A, Kopf BS, Edwards MR, Johnston SL, Casaulta C, Kieninger E, Jung A, Moeller A, Geiser T, Regamey N, et al., Novel antiviral properties of azithromycin in cystic fibrosis airway epithelial cells. Eur Respir J 2015; 45: 428-439.
-
(2015)
Eur Respir J
, vol.45
, pp. 428-439
-
-
Schogler, A.1
Kopf, B.S.2
Edwards, M.R.3
Johnston, S.L.4
Casaulta, C.5
Kieninger, E.6
Jung, A.7
Moeller, A.8
Geiser, T.9
Regamey, N.10
-
64
-
-
84925023856
-
Inhalation of macrolides: A novel approach to treatment of pulmonary infections
-
Siekmeier R, Hofmann T, Scheuch G,. Inhalation of macrolides: a novel approach to treatment of pulmonary infections. Adv Exp Med Biol 2015; 839: 13-24.
-
(2015)
Adv Exp Med Biol
, vol.839
, pp. 13-24
-
-
Siekmeier, R.1
Hofmann, T.2
Scheuch, G.3
-
65
-
-
0028914667
-
Effect of high-dose ibuprofen in patients with cystic fibrosis
-
Konstan MW, Byard PJ, Hoppel CL, Davis PB,. Effect of high-dose ibuprofen in patients with cystic fibrosis. N Engl J Med 1995; 332: 848-854.
-
(1995)
N Engl J Med
, vol.332
, pp. 848-854
-
-
Konstan, M.W.1
Byard, P.J.2
Hoppel, C.L.3
Davis, P.B.4
-
66
-
-
36848999782
-
Clinical use of Ibuprofen is associated with slower FEV1 decline in children with cystic fibrosis
-
Konstan MW, Schluchter MD, Xue W, Davis PB,. Clinical use of Ibuprofen is associated with slower FEV1 decline in children with cystic fibrosis. Am J Respir Crit Care Med 2007; 176: 1084-1089.
-
(2007)
Am J Respir Crit Care Med
, vol.176
, pp. 1084-1089
-
-
Konstan, M.W.1
Schluchter, M.D.2
Xue, W.3
Davis, P.B.4
-
67
-
-
34548038663
-
High-dose ibuprofen in cystic fibrosis: Canadian safety and effectiveness trial
-
Lands LC, Milner R, Cantin AM, Manson D, Corey M,. High-dose ibuprofen in cystic fibrosis: Canadian safety and effectiveness trial. J Pediatr 2007; 151: 249-254.
-
(2007)
J Pediatr
, vol.151
, pp. 249-254
-
-
Lands, L.C.1
Milner, R.2
Cantin, A.M.3
Manson, D.4
Corey, M.5
-
68
-
-
36148951390
-
Ibuprofen therapy and nasal polyposis in cystic fibrosis patients
-
Lindstrom DR, Conley SF, Splaingard ML, Gershan WM,. Ibuprofen therapy and nasal polyposis in cystic fibrosis patients. J Otolaryngol 2007; 36: 309-314.
-
(2007)
J Otolaryngol
, vol.36
, pp. 309-314
-
-
Lindstrom, D.R.1
Conley, S.F.2
Splaingard, M.L.3
Gershan, W.M.4
-
69
-
-
84918785468
-
Ibuprofen rescues mutant cystic fibrosis transmembrane conductance regulator trafficking
-
Carlile GW, Robert R, Goepp J, Matthes E, Liao J, Kus B, Macknight SD, Rotin D, Hanrahan JW, Thomas DY,. Ibuprofen rescues mutant cystic fibrosis transmembrane conductance regulator trafficking. J Cyst Fibros 2015; 14: 16-25.
-
(2015)
J Cyst Fibros
, vol.14
, pp. 16-25
-
-
Carlile, G.W.1
Robert, R.2
Goepp, J.3
Matthes, E.4
Liao, J.5
Kus, B.6
Macknight, S.D.7
Rotin, D.8
Hanrahan, J.W.9
Thomas, D.Y.10
-
70
-
-
84878000440
-
Risk factors for bronchiectasis in children with cystic fibrosis
-
Investigators A.C.
-
Sly PD, Gangell CL, Chen L, Ware RS, Ranganathan S, Mott LS, Murray CP, Stick SM, Investigators AC,. Risk factors for bronchiectasis in children with cystic fibrosis. N Engl J Med 2013; 368: 1963-1970.
-
(2013)
N Engl J Med
, vol.368
, pp. 1963-1970
-
-
Sly, P.D.1
Gangell, C.L.2
Chen, L.3
Ware, R.S.4
Ranganathan, S.5
Mott, L.S.6
Murray, C.P.7
Stick, S.M.8
-
71
-
-
84887117428
-
Alpha1-Antitrypsin promotes SPLUNC1-mediated lung defense against Pseudomonas aeruginosa infection in mice
-
Jiang D, Persinger R, Wu Q, Gross A, Chu HW,. Alpha1-Antitrypsin promotes SPLUNC1-mediated lung defense against Pseudomonas aeruginosa infection in mice. Respir Res 2013; 14: 122.
-
(2013)
Respir Res
, vol.14
, pp. 122
-
-
Jiang, D.1
Persinger, R.2
Wu, Q.3
Gross, A.4
Chu, H.W.5
-
72
-
-
0025966879
-
Aerosol alpha 1-antitrypsin treatment for cystic fibrosis
-
McElvaney NG, Hubbard RC, Birrer P, Chernick MS, Caplan DB, Frank MM, Crystal RG,. Aerosol alpha 1-antitrypsin treatment for cystic fibrosis. Lancet 1991; 337: 392-394.
-
(1991)
Lancet
, vol.337
, pp. 392-394
-
-
McElvaney, N.G.1
Hubbard, R.C.2
Birrer, P.3
Chernick, M.S.4
Caplan, D.B.5
Frank, M.M.6
Crystal, R.G.7
-
73
-
-
84891638906
-
Nebulized and oral thiol derivatives for pulmonary disease in cystic fibrosis
-
Tam J, Nash EF, Ratjen F, Tullis E, Stephenson A,. Nebulized and oral thiol derivatives for pulmonary disease in cystic fibrosis. Cochrane Database Syst Rev 2013; 7: CD007168.
-
(2013)
Cochrane Database Syst Rev
, vol.7
, pp. CD007168
-
-
Tam, J.1
Nash, E.F.2
Ratjen, F.3
Tullis, E.4
Stephenson, A.5
-
74
-
-
84880170145
-
Inhalation treatment with glutathione in patients with cystic fibrosis. A randomized clinical trial
-
Griese M, Kappler M, Eismann C, Ballmann M, Junge S, Rietschel E, van Koningsbruggen-Rietschel S, Staab D, Rolinck-Werninghaus C, Mellies U, et al., Inhalation treatment with glutathione in patients with cystic fibrosis. A randomized clinical trial. Am J Respir Crit Care Med 2013; 188: 83-89.
-
(2013)
Am J Respir Crit Care Med
, vol.188
, pp. 83-89
-
-
Griese, M.1
Kappler, M.2
Eismann, C.3
Ballmann, M.4
Junge, S.5
Rietschel, E.6
Van Koningsbruggen-Rietschel, S.7
Staab, D.8
Rolinck-Werninghaus, C.9
Mellies, U.10
-
75
-
-
84876987955
-
Safety and early treatment effects of the CXCR2 antagonist SB-656933 in patients with cystic fibrosis
-
Investigators C.F.
-
Moss RB, Mistry SJ, Konstan MW, Pilewski JM, Kerem E, Tal-Singer R, Lazaar AL, Investigators CF,. Safety and early treatment effects of the CXCR2 antagonist SB-656933 in patients with cystic fibrosis. J Cyst Fibros 2013; 12: 241-248.
-
(2013)
J Cyst Fibros
, vol.12
, pp. 241-248
-
-
Moss, R.B.1
Mistry, S.J.2
Konstan, M.W.3
Pilewski, J.M.4
Kerem, E.5
Tal-Singer, R.6
Lazaar, A.L.7
-
76
-
-
84895069337
-
A randomized double blind, placebo controlled phase 2 trial of BIIL 284 BS (an LTB4 receptor antagonist) for the treatment of lung disease in children and adults with cystic fibrosis
-
Investigators et al
-
Konstan MW, Doring G, Heltshe SL, Lands LC, Hilliard KA, Koker P, Bhattacharya S, Staab A, Hamilton A, Investigators et al. A randomized double blind, placebo controlled phase 2 trial of BIIL 284 BS (an LTB4 receptor antagonist) for the treatment of lung disease in children and adults with cystic fibrosis. J Cyst Fibros 2014; 13: 148-155.
-
(2014)
J Cyst Fibros
, vol.13
, pp. 148-155
-
-
Konstan, M.W.1
Doring, G.2
Heltshe, S.L.3
Lands, L.C.4
Hilliard, K.A.5
Koker, P.6
Bhattacharya, S.7
Staab, A.8
Hamilton, A.9
|