-
1
-
-
0036529046
-
Inflammation, infection, and pulmonary function in infants and young children with cystic fibrosis
-
Dakin CJ, Numa AH, Wang H, et al. Inflammation, infection, and pulmonary function in infants and young children with cystic fibrosis. Am J Respir Crit Care Med 2002; 165: 904-910. (Pubitemid 34774655)
-
(2002)
American Journal of Respiratory and Critical Care Medicine
, vol.165
, Issue.7
, pp. 904-910
-
-
Dakin, C.J.1
Numa, A.H.2
Wang, H.3
Morton, J.R.4
Vertzyas, C.C.5
Henry, R.L.6
-
2
-
-
0030768159
-
Lower airway inflammation in infants and young children with cystic fibrosis
-
Armstrong DS, Grimwood K, Carlin JB, et al. Lower airway inflammation in infants and young children with cystic fibrosis. Am J Respir Crit Care Med 1997; 156: 1197-1204.
-
(1997)
Am J Respir Crit Care Med
, vol.156
, pp. 1197-1204
-
-
Armstrong, D.S.1
Grimwood, K.2
Carlin, J.B.3
-
3
-
-
0036789637
-
Early airway infection, inflammation, and lung function in cystic fibrosis
-
Nixon GM, Armstrong DS, Carzino R, et al. Early airway infection, inflammation, and lung function in cystic fibrosis. Arch Dis Child 2002; 87: 306-311.
-
(2002)
Arch Dis Child
, vol.87
, pp. 306-311
-
-
Nixon, G.M.1
Armstrong, D.S.2
Carzino, R.3
-
4
-
-
75849161721
-
Cystic fibrosis lung disease starts in the small airways: Can we treat it more effectively?
-
Tiddens HA, Donaldson SH, Rosenfeld M, et al. Cystic fibrosis lung disease starts in the small airways: can we treat it more effectively? Pediatr Pulmonol 2010; 45: 107-117.
-
(2010)
Pediatr Pulmonol
, vol.45
, pp. 107-117
-
-
Tiddens, H.A.1
Donaldson, S.H.2
Rosenfeld, M.3
-
5
-
-
67650712233
-
Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening
-
Sly PD, Brennan S, Gangell C, et al. Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening. Am J Respir Crit Care Med 2009; 180: 146-152.
-
(2009)
Am J Respir Crit Care Med
, vol.180
, pp. 146-152
-
-
Sly, P.D.1
Brennan, S.2
Gangell, C.3
-
6
-
-
70349831005
-
Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening
-
Stick SM, Brennan S, Murray C, et al. Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening. J Pediatr 2009; 155: 623-628.
-
(2009)
J Pediatr
, vol.155
, pp. 623-628
-
-
Stick, S.M.1
Brennan, S.2
Murray, C.3
-
7
-
-
57149116921
-
Lung function in infants with cystic fibrosis diagnosed by newborn screening
-
Linnane BM, Hall GL, Nolan G, et al. Lung function in infants with cystic fibrosis diagnosed by newborn screening. Am J Respir Crit Care Med 2008; 178: 1238-1244.
-
(2008)
Am J Respir Crit Care Med
, vol.178
, pp. 1238-1244
-
-
Linnane, B.M.1
Hall, G.L.2
Nolan, G.3
-
8
-
-
12744277962
-
Multiple-breath washout as a marker of lung disease in preschool children with cystic fibrosis
-
Aurora P, Bush A, Gustafsson P, et al. Multiple-breath washout as a marker of lung disease in preschool children with cystic fibrosis. Am J Respir Crit Care Med 2005; 171: 249-256.
-
(2005)
Am J Respir Crit Care Med
, vol.171
, pp. 249-256
-
-
Aurora, P.1
Bush, A.2
Gustafsson, P.3
-
9
-
-
0024990329
-
The role of mucous glycoproteins in the rheologic properties of cystic fibrosis sputum
-
Lethem MI, James SL, Marriott C. The role of mucous glycoproteins in the rheologic properties of cystic fibrosis sputum. Am Rev Respir Dis 1990; 142: 1053-1058. (Pubitemid 20384359)
-
(1990)
American Review of Respiratory Disease
, vol.142
, Issue.5
, pp. 1053-1058
-
-
Lethem, M.I.1
James, S.L.2
Marriott, C.3
-
10
-
-
0025647882
-
Recombinant human DNase I reduces the viscosity of cystic fibrosis sputum
-
Shak S, Capon DJ, Hellmiss R, et al. Recombinant human DNase I reduces the viscosity of cystic fibrosis sputum. Proc Natl Acad Sci USA 1990; 87: 9188-9192. (Pubitemid 120030590)
-
(1990)
Proceedings of the National Academy of Sciences of the United States of America
, vol.87
, Issue.23
, pp. 9188-9192
-
-
Shak, S.1
Capon, D.J.2
Hellmiss, R.3
Marsters, S.A.4
Baker, C.L.5
-
11
-
-
0028129568
-
Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis
-
DOI 10.1056/NEJM199409083311003
-
Fuchs HJ, Borowitz DS, Christiansen DH, 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. (Pubitemid 24276863)
-
(1994)
New England Journal of Medicine
, vol.331
, Issue.10
, 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
-
12
-
-
0028790503
-
DNase trials in cystic fibrosis
-
Hodson ME, Shah PL. DNase trials in cystic fibrosis. Eur Respir J 1995; 8: 1786-1791.
-
(1995)
Eur Respir J
, vol.8
, pp. 1786-1791
-
-
Hodson, M.E.1
Shah, P.L.2
-
13
-
-
0035666058
-
A two-year randomized, placebo-controlled trial of dornase alfa in young patients with cystic fibrosis with mild lung function abnormalities
-
DOI 10.1067/mpd.2001.118570
-
Quan JM, Tiddens HA, Sy JP, 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. (Pubitemid 34014460)
-
(2001)
Journal of Pediatrics
, vol.139
, Issue.6
, pp. 813-820
-
-
Quan, J.M.1
Tiddens, H.A.W.M.2
Sy, J.P.3
McKenzie, S.G.4
Montgomery, M.D.5
Robinson, P.J.6
Wohl, M.E.B.7
Konstan, M.W.8
-
14
-
-
39049084491
-
Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis
-
DOI 10.1136/thx.2007.077784
-
Gustafsson PM, De Jong PA, Tiddens HA, et al. Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis. Thorax 2008; 63: 129-134. (Pubitemid 351236476)
-
(2008)
Thorax
, vol.63
, Issue.2
, pp. 129-134
-
-
Gustafsson, P.M.1
De Jong, P.A.2
Tiddens, H.A.W.M.3
Lindblad, A.4
-
15
-
-
46349106358
-
Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis
-
DOI 10.1164/rccm.200710-1599OC
-
Kozlowska WJ, Bush A, Wade A, et al. Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis. Am J Respir Crit Care Med 2008; 178: 42-49. (Pubitemid 351919192)
-
(2008)
American Journal of Respiratory and Critical Care Medicine
, vol.178
, Issue.1
, pp. 42-49
-
-
Kozlowska, W.J.1
Bush, A.2
Wade, A.3
Aurora, P.4
Carr, S.B.5
Castle, R.A.6
Hoo, A.-F.7
Lum, S.8
Price, J.9
Ranganathan, S.10
Saunders, C.11
Stanojevic, S.12
Stroobant, J.13
Wallis, C.14
Stocks, J.15
Lynn, I.B.16
Davies, J.17
Dinwidle, R.18
Oliver, C.19
Rosenthal, M.20
Ruiz, G.21
Shankar, A.22
Stocks, J.23
Suri, R.24
Wyatt, H.25
more..
-
16
-
-
0037090744
-
Clinical findings and lung pathology in children with cystic fibrosis
-
Hamutcu R, Rowland JM, Horn MV, et al. Clinical findings and lung pathology in children with cystic fibrosis. Am J Respir Crit Care Med 2002; 165: 1172-1175. (Pubitemid 34415829)
-
(2002)
American Journal of Respiratory and Critical Care Medicine
, vol.165
, Issue.8
, pp. 1172-1175
-
-
Hamutcu, R.1
Rowland, J.M.2
Horn, M.V.3
Kaminsky, C.4
MacLaughlin, E.F.5
Starnes, V.A.6
Woo, M.S.7
-
17
-
-
0034081090
-
Cartilaginous airway wall dimensions and airway resistance in cystic fibrosis lungs
-
DOI 10.1034/j.1399-3003.2000.15d18.x
-
Tiddens HA, Koopman LP, Lambert RK, et al. Cartilaginous airway wall dimensions and airway resistance in cystic fibrosis lungs. Eur Respir J 2000; 15: 735-742. (Pubitemid 30196303)
-
(2000)
European Respiratory Journal
, vol.15
, Issue.4
, pp. 735-742
-
-
Tiddens, H.A.W.M.1
Koopman, L.P.2
Lambert, R.K.3
Elliott, W.M.4
Hop, W.C.J.5
Van Der, M.T.W.6
De Boer, W.J.7
De Jongste, J.C.8
-
18
-
-
50849121702
-
Small airways disease in cystic fibrosis
-
Brownlee KG. Small airways disease in cystic fibrosis. Eur Respir Mon 2006; 35: 21-37.
-
(2006)
Eur Respir Mon
, vol.35
, pp. 21-37
-
-
Brownlee, K.G.1
-
19
-
-
0030656515
-
RhDNase I aerosol deposition and related factors in cystic fibrosis
-
Diot P, Palmer LB, Smaldone A, et al. RhDNase I aerosol deposition and related factors in cystic fibrosis. Am J Respir Crit Care Med 1997; 156: 1662-1668. (Pubitemid 27505540)
-
(1997)
American Journal of Respiratory and Critical Care Medicine
, vol.156
, Issue.5
, pp. 1662-1668
-
-
Diot, P.1
Palmer, L.B.2
Smaldone, A.3
Decelie-Germana, J.4
Grimson, R.5
Smaldone, G.C.6
-
20
-
-
0033786617
-
Targeting aerosol deposition in patients with cystic fibrosis: Effects of alterations in particle size and inspiratory flow rate
-
Laube BL, Jashnani R, Dalby RN, et al. Targeting aerosol deposition in patients with cystic fibrosis: effects of alterations in particle size and inspiratory flow rate. Chest 2000; 118: 1069-1076.
-
(2000)
Chest
, vol.118
, pp. 1069-1076
-
-
Laube, B.L.1
Jashnani, R.2
Dalby, R.N.3
-
21
-
-
14844322136
-
Optimum peripheral drug deposition in patients with cystic fibrosis
-
DOI 10.1089/jam.2005.18.45
-
Brand P, Meyer T, Haussermann S, et al. Optimum peripheral drug deposition in patients with cystic fibrosis. J Aerosol Med 2005; 18: 45-54. (Pubitemid 40349946)
-
(2005)
Journal of Aerosol Medicine: Deposition, Clearance, and Effects in the Lung
, vol.18
, Issue.1
, pp. 45-54
-
-
Brand, P.1
Meyer, T.2
Haussermann, S.3
Schulte, M.4
Scheuch, G.5
Bernhard, T.6
Sommerauer, B.7
Weber, N.8
Griese, M.9
-
22
-
-
0042026773
-
1-protease inhibitor using commercial inhalation devices
-
DOI 10.1183/09031936.03.00096802
-
Brand P, Beckmann H, Maas Enriquez M, et al. Peripheral deposition of alpha1-protease inhibitor using commercial inhalation devices. Eur Respir J 2003; 22: 263-267. (Pubitemid 36986995)
-
(2003)
European Respiratory Journal
, vol.22
, Issue.2
, pp. 263-267
-
-
Brand, P.1
Maas, E.M.2
Meyer, T.3
Mllinger, B.4
Sommerer, K.5
Weber, N.6
Weuthen, T.7
Scheuch, G.8
-
23
-
-
12144289811
-
Improvement of alveolar glutathione and lung function but not oxidative state in cystic fibrosis
-
Griese M, Ramakers J, Krasselt A, et al. Improvement of alveolar glutathione and lung function but not oxidative state in cystic fibrosis. Am J Respir Crit Care Med 2004; 169: 822-828. (Pubitemid 38402458)
-
(2004)
American Journal of Respiratory and Critical Care Medicine
, vol.169
, Issue.7
, pp. 822-828
-
-
Griese, M.1
Ramakers, J.2
Krasselt, A.3
Starosta, V.4
Van Koningsbruggen, S.5
Fischer, R.6
Ratjen, F.7
Mullinger, B.8
Huber, R.M.9
Maier, K.10
Rietschel, E.11
Scheuch, G.12
-
24
-
-
29844456892
-
Lung deposition after electronically breath-controlled inhalation and manually triggered conventional inhalation in cystic fibrosis patients
-
DOI 10.1089/jam.2005.18.386
-
Kohler E, Sollich V, Schuster-Wonka R, et al. Lung deposition after electronically breath-controlled inhalation and manually triggered conventional inhalation in cystic fibrosis patients. J Aerosol Med 2005; 18: 386-395. (Pubitemid 43038405)
-
(2005)
Journal of Aerosol Medicine: Deposition, Clearance, and Effects in the Lung
, vol.18
, Issue.4
, pp. 386-395
-
-
Kohler, E.1
Sollich, V.2
Schuster-Wonka, R.3
Jorch, G.4
-
25
-
-
84860314786
-
Optimizing aerosol lung deposition in cystic fibrosis patients
-
Romano L, Manno G, Galietta LJV, eds. Bologna, Monduzzi Editore
-
Scheuch G, Müllinger B, Brand P, et al. Optimizing aerosol lung deposition in cystic fibrosis patients. In: Romano L, Manno G, Galietta LJV, eds. Proceedings of the 25th European Cystic Fibrosis Conference. Bologna, Monduzzi Editore, 2002; pp. 169-172.
-
(2002)
Proceedings of the 25th European Cystic Fibrosis Conference
, pp. 169-172
-
-
Scheuch, G.1
Müllinger, B.2
Brand, P.3
-
27
-
-
0031445242
-
Comparison of drug delivery from conventional versus 'Venturi' nebulizers
-
DOI 10.1183/09031936.97.10112479
-
Devadason SG, Everard ML, Linto JM, et al. Comparison of drug delivery from conventional versus "Venturi" nebulizers. Eur Respir J 1997; 10: 2479-2483. (Pubitemid 28048619)
-
(1997)
European Respiratory Journal
, vol.10
, Issue.11
, pp. 2479-2483
-
-
Devadason, S.G.1
Everard, M.L.2
Linto, J.M.3
Le, S.P.N.4
-
28
-
-
1542317673
-
Performance comparison of nebulizer designs: Constant-output, breath-enhanced, and dosimetric
-
Rau JL, Ari A, Restrepo RD. Performance comparison of nebulizer designs: constant-output, breath-enhanced, and dosimetric. Respir Care 2004; 49: 174-179.
-
(2004)
Respir Care
, vol.49
, pp. 174-179
-
-
Rau, J.L.1
Ari, A.2
Restrepo, R.D.3
-
29
-
-
0028228536
-
Efficient drug delivery to the lungs from a continuously operated open-vent nebulizer and low pressure compressor system
-
Newman SP, Pitcairn GR, Hooper G, et al. Efficient drug delivery to the lungs from a continuously operated open-vent nebulizer and low pressure compressor system. Eur Respir J 1994; 7: 1177-1181. (Pubitemid 24187340)
-
(1994)
European Respiratory Journal
, vol.7
, Issue.6
, pp. 1177-1181
-
-
Newman, S.P.1
Pitcairn, G.R.2
Hooper, G.3
Knoch, M.4
-
30
-
-
0027165064
-
Lung deposition from four nebulizers
-
DOI 10.1016/0954-6111(93)90074-A
-
Hardy JG, Newman SP, Knoch M. Lung deposition from four nebulizers. Respir Med 1993; 87: 461-465. (Pubitemid 23266355)
-
(1993)
Respiratory Medicine
, vol.87
, Issue.6
, pp. 461-465
-
-
Hardy, J.G.1
Newman, S.P.2
Knoch, M.3
-
31
-
-
24644519265
-
Titrating steroids on exhaled nitric oxide in children with asthma: A randomized controlled trial
-
DOI 10.1164/rccm.200503-458OC
-
Pijnenburg MW, Bakker EM, Hop WC, et al. Titrating steroids on exhaled nitric oxide in children with asthma: a randomized controlled trial. Am J Respir Crit Care Med 2005; 172: 831-836. (Pubitemid 41369065)
-
(2005)
American Journal of Respiratory and Critical Care Medicine
, vol.172
, Issue.7
, pp. 831-836
-
-
Pijnenburg, M.W.1
Bakker, E.M.2
Hop, W.C.3
De Jongste, J.C.4
-
32
-
-
9844267303
-
One year treatment with salmeterol compared with beclomethasone in children with asthma
-
Verberne AA, Frost C, Roorda RJ, et al. One year treatment with salmeterol compared with beclomethasone in children with asthma. The Dutch Paediatric Asthma Study Group. Am J Respir Crit Care Med 1997; 156: 688-695. (Pubitemid 27396402)
-
(1997)
American Journal of Respiratory and Critical Care Medicine
, vol.156
, Issue.3 I
, pp. 688-695
-
-
Verberne, A.A.P.H.1
Frost, C.2
Roorda, R.J.3
Van Der, L.H.4
Kerrebijn, K.F.5
Raaymakers, J.A.M.6
Pocock, S.J.7
Bogaard, J.M.8
Van Nierop, J.C.9
Nagelkerke, A.F.10
Dankert-Roelse, J.E.11
Thio, B.12
Schouten, T.J.13
Van Essen-Zandvliet, E.E.M.14
Denteneer, A.15
Gerritsen, J.16
Grol, M.17
Hendriks, J.J.E.18
Duiverman, E.J.19
Kouwenberg, J.M.20
Brackel, H.J.L.21
more..
-
33
-
-
34347395936
-
RhDNase before airway clearance therapy improves airway patency in children with CF
-
DOI 10.1002/ppul.20636
-
van der Giessen LJ, de Jongste JC, Gosselink R, et al. RhDNase before airway clearance therapy improves airway patency in children with CF. Pediatr Pulmonol 2007; 42: 624-630. (Pubitemid 47021055)
-
(2007)
Pediatric Pulmonology
, vol.42
, Issue.7
, pp. 624-630
-
-
Van Der, G.L.J.1
De Jongste, J.C.2
Gosselink, R.3
Hop, W.C.J.4
Tiddens, H.A.W.M.5
-
34
-
-
38849129311
-
Reference ranges for spirometry across all ages: A new approach
-
DOI 10.1164/rccm.200708-1248OC
-
Stanojevic S, Wade A, Stocks J, et al. Reference ranges for spirometry across all ages: a new approach. Am J Respir Crit Care Med 2008; 177: 253-260. (Pubitemid 351198367)
-
(2008)
American Journal of Respiratory and Critical Care Medicine
, vol.177
, Issue.3
, pp. 253-260
-
-
Stanojevic, S.1
Wade, A.2
Stocks, J.3
Hankinson, J.4
Coates, A.L.5
Pan, H.6
Rosenthal, M.7
Corey, M.8
Lebecque, P.9
Cole, T.J.10
-
35
-
-
0017611938
-
DIE BEDEUTUNG HEUTIGER METHODEN DER LUNGENFUNKTIONSDIAGNOSTIK ZUR FESTSTELLUNG EINER OBSTRUKTION DER ATEMWEGE BEI KINDERN UND JUGENDLICHEN
-
Zapletal A, Paul T, Samanek M. Die Bedeutung heutiger Methoden der Lungenfunktionsdiagnostik zur Feststellung einer Obstruktion der Atemwege bei Kindern und Jugendlichen [Significance of contemporary methods of lung function testing for the detection of airway obstruction in children and adolescents]. Z Erkr Atmungsorgane 1977; 149: 343-371. (Pubitemid 8264588)
-
(1977)
Zeitschrift fur Erkrankungen der Atmungsorgane
, vol.149
, Issue.3
, pp. 343-371
-
-
Zapletal, A.1
Paul, T.2
Samanek, M.3
-
36
-
-
33745994280
-
A multi-method assessment of treatment adherence for children with cystic fibrosis
-
DOI 10.1016/j.jcf.2006.03.002, PII S1569199306000348
-
Modi AC, Lim CS, Yu N, et al. A multi-method assessment of treatment adherence for children with cystic fibrosis. J Cyst Fibros 2006; 5: 177-185. (Pubitemid 44063951)
-
(2006)
Journal of Cystic Fibrosis
, vol.5
, Issue.3
, pp. 177-185
-
-
Modi, A.C.1
Lim, C.S.2
Yu, N.3
Geller, D.4
Wagner, M.H.5
Quittner, A.L.6
-
37
-
-
0036898857
-
Nebulised dornase alpha: Adherence in adults with cystic fibrosis
-
Burrows JA, Bunting JP, Masel PJ, et al. Nebulised dornase alpha: adherence in adults with cystic fibrosis. J Cyst Fibros 2002; 1: 255-259.
-
(2002)
J Cyst Fibros
, vol.1
, pp. 255-259
-
-
Burrows, J.A.1
Bunting, J.P.2
Masel, P.J.3
-
38
-
-
61349198184
-
Adherence to nebulised antibiotics in cystic fibrosis
-
Latchford G, Duff A, Quinn J, et al. Adherence to nebulised antibiotics in cystic fibrosis. Patient Educ Couns 2009; 75: 141-144.
-
(2009)
Patient Educ Couns
, vol.75
, pp. 141-144
-
-
Latchford, G.1
Duff, A.2
Quinn, J.3
-
39
-
-
0027278897
-
Efficacy and safety of short-term administration of aerosolized recombinant human deoxyribonuclease in patients with cystic fibrosis
-
Ramsey BW, Astley SJ, Aitken ML, et al. Efficacy and safety of short-term administration of aerosolized recombinant human deoxyribonuclease in patients with cystic fibrosis. Am Rev Respir Dis 1993; 148: 145-151. (Pubitemid 23187234)
-
(1993)
American Review of Respiratory Disease
, vol.148
, Issue.1
, pp. 145-151
-
-
Ramsey, B.W.1
Astley, S.J.2
Aitken, M.L.3
Burke, W.4
Colin, A.A.5
Dorkin, H.L.6
Eisenberg, J.D.7
Gibson, R.L.8
Harwood, I.R.9
Schidlow, D.V.10
Wilmott, R.W.11
Wohl, M.E.12
Meyerson, L.J.13
Shak, S.14
Fuchs, H.15
Smith, A.L.16
-
40
-
-
0030923835
-
An evaluation of two aerosol delivery systems for rhDNase
-
DOI 10.1183/09031936.97.10061261
-
Shah PL, Scott SF, Geddes DM, et al. An evaluation of two aerosol delivery systems for rhDNase. Eur Respir J 1997; 10: 1261-1266. (Pubitemid 27278243)
-
(1997)
European Respiratory Journal
, vol.10
, Issue.6
, pp. 1261-1266
-
-
Shah, P.L.1
Scott, S.F.2
Geddes, D.M.3
Conway, S.4
Watson, A.5
Nazir, T.6
Carr, S.B.7
Wallis, C.8
Marriott, C.9
Hodson, M.E.10
-
41
-
-
0031936645
-
Effect of smaller droplet size of dornase alfa on lung function in mild cystic fibrosis
-
DOI 10.1002/(SICI)1099-0496(199802)25:2<83::AID-PPUL2>3.0.CO;2-O
-
Geller DE, Eigen H, Fiel SB, et al. Effect of smaller droplet size of dornase alfa on lung function in mild cystic fibrosis. Dornase Alfa Nebulizer Group. Pediatr Pulmonol 1998; 25: 83-87. (Pubitemid 28110582)
-
(1998)
Pediatric Pulmonology
, vol.25
, Issue.2
, pp. 83-87
-
-
Geller, D.E.1
Eigen, H.2
Fiel, S.B.3
Clark, A.4
Lamarre, A.P.5
Johnson, C.A.6
Konstan, M.W.7
-
42
-
-
0038132084
-
Bolus inhalation of rhDNAse with the AERx system in subjects with cystic fibrosis
-
DOI 10.1089/089426803321919933
-
Geller D, Thipphawong J, Otulana B, et al. Bolus inhalation of rhDNase with the AERx system in subjects with cystic fibrosis. J Aerosol Med 2003; 16: 175-182. (Pubitemid 36702671)
-
(2003)
Journal of Aerosol Medicine: Deposition, Clearance, and Effects in the Lung
, vol.16
, Issue.2
, pp. 175-182
-
-
Geller, D.1
Thipphawong, J.2
Otulana, B.3
Caplan, D.4
Ericson, D.5
Milgram, L.6
Okikawa, J.7
Quan, J.8
Bowman, C.M.9
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