-
1
-
-
50649123290
-
CFTR function and prospects for therapy
-
Riordan JR. CFTR function and prospects for therapy. Annu Rev Biochem 2008;77:701-726.
-
(2008)
Annu Rev Biochem
, vol.77
, pp. 701-726
-
-
Riordan, J.R.1
-
2
-
-
33845992179
-
Evidence for airway surface dehydration as the initiating event in CF airway disease
-
DOI 10.1111/j.1365-2796.2006.01744.x
-
Boucher RC. Evidence for airway surface dehydration as the initiating event in CF airway disease. J Intern Med 2007;261:5-16. (Pubitemid 46046468)
-
(2007)
Journal of Internal Medicine
, vol.261
, Issue.1
, pp. 5-16
-
-
Boucher, R.C.1
-
3
-
-
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, Aurora P, Carr SB, Castle RA, Hoo AF, Lum S, Price J, Ranganathan S, et al.; London Cystic Fibrosis Collaboration. 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..
-
4
-
-
57149116921
-
Lung function in infants with cystic fibrosis diagnosed by newborn screening
-
Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST-CF)
-
Linnane BM, Hall GL, Nolan G, Brennan S, Stick SM, Sly PD, Robertson CF, Robinson PJ, Franklin PJ, Turner SW, et al.; Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST-CF). 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
Brennan, S.4
Stick, S.M.5
Sly, P.D.6
Robertson, C.F.7
Robinson, P.J.8
Franklin, P.J.9
Turner, S.W.10
-
5
-
-
1542287428
-
Structural airway abnormalities in infants and young children with cystic fibrosis
-
DOI 10.1016/j.jpeds.2003.09.026, PII S0022347603006115
-
Long FR, Williams RS, Castile RG. Structural airway abnormalities in infants and young children with cystic fibrosis. J Pediatr 2004;144:154-161. (Pubitemid 38869388)
-
(2004)
Journal of Pediatrics
, vol.144
, Issue.2
, pp. 154-161
-
-
Long, F.R.1
Williams, R.S.2
Castile, R.G.3
-
6
-
-
67650712233
-
Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening
-
Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST-CF)
-
Sly PD, Brennan S, Gangell C, de Klerk N, Murray C, Mott L, Stick SM, Robinson PJ, Robertson CF, Ranganathan SC, et al.; Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST-CF). 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
De Klerk, N.4
Murray, C.5
Mott, L.6
Stick, S.M.7
Robinson, P.J.8
Robertson, C.F.9
Ranganathan, S.C.10
-
7
-
-
70349831005
-
Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening
-
Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST-CF)
-
Stick SM, Brennan S, Murray C, Douglas T, von Ungern-Sternberg BS, Garratt LW, Gangell CL, De Klerk N, Linnane B, Ranganathan S, et al.; Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST-CF). Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening. J Pediatr 2009;155:623-628.e1.
-
(2009)
J Pediatr
, vol.155
-
-
Stick, S.M.1
Brennan, S.2
Murray, C.3
Douglas, T.4
Von Ungern-Sternberg, B.S.5
Garratt, L.W.6
Gangell, C.L.7
De Klerk, N.8
Linnane, B.9
Ranganathan, S.10
-
8
-
-
73449113631
-
Measuring and improving respiratory outcomes in cystic fibrosis lung disease: Opportunities and challenges to therapy
-
Zemanick ET, Harris JK, Conway S, Konstan MW, Marshall B, Quittner AL, Retsch-Bogart G, Saiman L, Accurso FJ. Measuring and improving respiratory outcomes in cystic fibrosis lung disease: opportunities and challenges to therapy. J Cyst Fibros 2010;9:1-16.
-
(2010)
J Cyst Fibros
, vol.9
, pp. 1-16
-
-
Zemanick, E.T.1
Harris, J.K.2
Conway, S.3
Konstan, M.W.4
Marshall, B.5
Quittner, A.L.6
Retsch-Bogart, G.7
Saiman, L.8
Accurso, F.J.9
-
9
-
-
75849161721
-
Cystic fibrosis lung disease starts in the small airways: Can we treat it more effectively?
-
Tiddens HAWM, Donaldson SH, Rosenfeld M, Pare PD. 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
-
-
Hawm, T.1
Donaldson, S.H.2
Rosenfeld, M.3
Pare, P.D.4
-
10
-
-
48949088690
-
Early detection of lung disease in children with cystic fibrosis using lung function
-
Ranganathan S, Linnane B, Nolan G, Gangell C, Hall G. Early detection of lung disease in children with cystic fibrosis using lung function. Paediatr Respir Rev 2008;9:160-167.
-
(2008)
Paediatr Respir Rev
, vol.9
, pp. 160-167
-
-
Ranganathan, S.1
Linnane, B.2
Nolan, G.3
Gangell, C.4
Hall, G.5
-
11
-
-
54949112835
-
TMEM16A, a membrane protein associated with calcium-dependent chloride channel activity
-
Caputo A, Caci E, Ferrera L, Pedemonte N, Barsanti C, Sondo E, Pfeffer U, Ravazzolo R, Zegarra-Moran O, Galietta LJ. TMEM16A, a membrane protein associated with calcium-dependent chloride channel activity. Science 2008;322:590-594.
-
(2008)
Science
, vol.322
, pp. 590-594
-
-
Caputo, A.1
Caci, E.2
Ferrera, L.3
Pedemonte, N.4
Barsanti, C.5
Sondo, E.6
Pfeffer, U.7
Ravazzolo, R.8
Zegarra-Moran, O.9
Galietta, L.J.10
-
12
-
-
55249091085
-
TMEM16A confers receptor-activated calcium-dependent chloride conductance
-
Yang YD, Cho H, Koo JY, Tak MH, Cho Y, Shim WS, Park SP, Lee J, Lee B, Kim BM, et al. TMEM16A confers receptor-activated calcium-dependent chloride conductance. Nature 2008;455:1210-1215.
-
(2008)
Nature
, vol.455
, pp. 1210-1215
-
-
Yang, Y.D.1
Cho, H.2
Koo, J.Y.3
Tak, M.H.4
Cho, Y.5
Shim, W.S.6
Park, S.P.7
Lee, J.8
Lee, B.9
Kim, B.M.10
-
13
-
-
51549120559
-
Expression cloning of TMEM16A as a calcium-activated chloride channel subunit
-
Schroeder BC, Cheng T, Jan YN, Jan LY. Expression cloning of TMEM16A as a calcium-activated chloride channel subunit. Cell 2008;134:1019-1029.
-
(2008)
Cell
, vol.134
, pp. 1019-1029
-
-
Schroeder, B.C.1
Cheng, T.2
Jan, Y.N.3
Jan, L.Y.4
-
14
-
-
0036720462
-
2receptor agonist for the treatment of cystic fibrosis
-
DOI 10.1124/jpet.102.035485
-
Yerxa BR, Sabater JR, Davis CW, Stutts MJ, Lang-Furr M, Picher M, Jones AC, Cowlen M, Dougherty R, Boyer J, et al. Pharmacology of INS37217 [P1-(uridine 5′)-P4- (2′-deoxycytidine 5′)tetraphosphate, tetrasodium salt], a next-generation P2Y2 receptor agonist for the treatment of cystic fibrosis. J Pharmacol Exp Ther 2002;302:871-880. (Pubitemid 34920206)
-
(2002)
Journal of Pharmacology and Experimental Therapeutics
, vol.302
, Issue.3
, pp. 871-880
-
-
Yerxa, B.R.1
Sabater, J.R.2
Davis, C.W.3
Stutts, M.J.4
Lang-Furr, M.5
Picher, M.6
Jones, A.C.7
Cowlen, M.8
Dougherty, R.9
Boyer, J.10
Abraham, W.M.11
Boucher, R.C.12
-
15
-
-
67649344455
-
Transmembrane protein 16A (TMEM16A) is a Ca2+-regulated Cl- Secretory channel in mouse airways
-
Rock JR, O'Neal WK, Gabriel SE, Randell SH, Harfe BD, Boucher RC, Grubb BR. Transmembrane protein 16A (TMEM16A) is a Ca2+-regulated Cl- secretory channel in mouse airways. J Biol Chem 2009;284:14875-14880.
-
(2009)
J Biol Chem
, vol.284
, pp. 14875-14880
-
-
Rock, J.R.1
O'Neal, W.K.2
Gabriel, S.E.3
Randell, S.H.4
Harfe, B.D.5
Boucher, R.C.6
Grubb, B.R.7
-
16
-
-
47049114203
-
2 agonists that led to Phase 3
-
DOI 10.1016/j.pupt.2007.12.003, PII S1094553907001046
-
Kellerman D, Rossi Mospan A, Engels J, Schaberg A, Gorden J, Smiley L. Denufosol: a review of studies with inhaled P2Y2 agonists that led to phase 3. Pulm Pharmacol Ther 2008;21:600-607. (Pubitemid 351970709)
-
(2008)
Pulmonary Pharmacology and Therapeutics
, vol.21
, Issue.4
, pp. 600-607
-
-
Kellerman, D.1
Rossi, M.A.2
Engels, J.3
Schaberg, A.4
Gorden, J.5
Smiley, L.6
-
17
-
-
11244283223
-
2
-
DOI 10.1096/fj.04-2314fje
-
Kunzelmann K, Bachhuber T, Regeer R, Markovich D, Sun J, Schreiber R. Purinergic inhibition of the epithelial Na+ transport via hydrolysis of PIP2. FASEB J 2005;19:142-143. (Pubitemid 40069945)
-
(2005)
FASEB Journal
, vol.19
, Issue.1
, pp. 142-143
-
-
Kunzelmann, K.1
Bachhuber, T.2
Regeer, R.3
Markovich, D.4
Sun, J.5
Schreiber, R.6
-
19
-
-
20144363443
-
Safety and tolerability of denufosol tetrasodium inhalation solution, a novel P2Y2 receptor agonist: Results of a phase 1/phase 2 multicenter study in mild to moderate cystic fibrosis
-
Cystic Fibrosis Foundation Therapeutics Development Network
-
Deterding R, Retsch-Bogart G, Milgram L, Gibson R, Daines C, Zeitlin PL, Milla C, Marshall B, Lavange L, Engels J, et al.; Cystic Fibrosis Foundation Therapeutics Development Network. Safety and tolerability of denufosol tetrasodium inhalation solution, a novel P2Y2 receptor agonist: results of a phase 1/phase 2 multicenter study in mild to moderate cystic fibrosis. Pediatr Pulmonol 2005;39:339-348.
-
(2005)
Pediatr Pulmonol
, vol.39
, pp. 339-348
-
-
Deterding, R.1
Retsch-Bogart, G.2
Milgram, L.3
Gibson, R.4
Daines, C.5
Zeitlin, P.L.6
Milla, C.7
Marshall, B.8
Lavange, L.9
Engels, J.10
-
20
-
-
34547949974
-
Phase 2 randomized safety and efficacy trial of nebulized denufosol tetrasodium in cystic fibrosis
-
DOI 10.1164/rccm.200608-1238OC
-
Deterding RR, LaVange LM, Engels JM, Mathews DW, Coquillette SJ, Brody AS, Millard SP, Ramsey BW; Cystic Fibrosis Therapeutics Development Network and the Inspire 08-103Working Group. Phase 2 randomized safety and efficacy trial of nebulized denufosol tetrasodium in cystic fibrosis. Am J Respir Crit Care Med 2007;176:362-369. (Pubitemid 47267470)
-
(2007)
American Journal of Respiratory and Critical Care Medicine
, vol.176
, Issue.4
, pp. 362-369
-
-
Deterding, R.R.1
LaVange, L.M.2
Engels, J.M.3
Mathews, D.W.4
Coquillette, S.J.5
Brody, A.S.6
Millard, S.P.7
Ramsey, B.W.8
-
21
-
-
70349825055
-
Phase 3 study of denufosol tetrasodium for the treatment of cystic fibrosis [abstract]
-
Moss RB, Anbar RD, Wilmott RW, Barnes M, Schaberg AE, Durham TA, Accurso FJ. Phase 3 study of denufosol tetrasodium for the treatment of cystic fibrosis [abstract]. Am J Respir Crit Care Med 2009;179:A1189.
-
(2009)
Am J Respir Crit Care Med
, vol.179
-
-
Moss, R.B.1
Anbar, R.D.2
Wilmott, R.W.3
Barnes, M.4
Schaberg, A.E.5
Durham, T.A.6
Accurso, F.J.7
-
22
-
-
79952220258
-
Effects of denufosol on sinusitis-related complaints in a phase 3 trial in cystic fibrosis patients
-
abstract
-
Mospan AR, Durham TA, Schaberg AE, Accurso FJ. Effects of denufosol on sinusitis-related complaints in a phase 3 trial in cystic fibrosis patients [abstract]. J Cyst Fibros 2009;8:S26.
-
(2009)
J Cyst Fibros
, vol.8
-
-
Mospan, A.R.1
Durham, T.A.2
Schaberg, A.E.3
Accurso, F.J.4
-
23
-
-
79952232656
-
Relationship between pulmonary exacerbations and lung function decline in a six month trial of denufosol
-
abstract
-
Accurso FJ, Durham TA, Schaberg AE. Relationship between pulmonary exacerbations and lung function decline in a six month trial of denufosol [abstract]. J Cyst Fibros 2009;8:S26.
-
(2009)
J Cyst Fibros
, vol.8
-
-
Accurso, F.J.1
Durham, T.A.2
Schaberg, A.E.3
-
24
-
-
79952226472
-
Pharmacological treatment of CF: Lessons learned from a phase 3 clinical trial
-
abstract
-
Navratil T, Schaberg A, Mathews D, Deans C, Durham T, Accurso FJ. Pharmacological treatment of CF: lessons learned from a phase 3 clinical trial [abstract]. Pediatr Pulmonol Suppl 2009;32:416.
-
(2009)
Pediatr Pulmonol Suppl
, vol.32
, pp. 416
-
-
Navratil, T.1
Schaberg, A.2
Mathews, D.3
Deans, C.4
Durham, T.5
Accurso, F.J.6
-
25
-
-
79952214835
-
Concomitant medication use in patients with mild cystic fibrosis lung disease assigned to placebo in Phase 3 clinical trial of denufosol (Study 08-108/TIGER-1)
-
abstract
-
Durham T, Navratil T, Schaberg A, Deans C, Smiley L, Herje N, Retsch-Bogart G, Accurso FJ. Concomitant medication use in patients with mild cystic fibrosis lung disease assigned to placebo in Phase 3 clinical trial of denufosol (Study 08-108/TIGER-1) [abstract]. Am J Respir Crit Care Med 2010;181:A1842.
-
(2010)
Am J Respir Crit Care Med
, vol.181
-
-
Durham, T.1
Navratil, T.2
Schaberg, A.3
Deans, C.4
Smiley, L.5
Herje, N.6
Retsch-Bogart, G.7
Accurso, F.J.8
-
26
-
-
79952204375
-
Potential of denufosol as an early intervention therapy for CF lung disease
-
abstract
-
Navratil T, Schaberg A, Tian W, Durham T, Evans C, Lindroos C, Barrus S, Mathews D, Barnes M, Ratjen F, et al. Potential of denufosol as an early intervention therapy for CF lung disease [abstract]. FASEB J 2010;24:31.
-
(2010)
FASEB J
, vol.24
, pp. 31
-
-
Navratil, T.1
Schaberg, A.2
Tian, W.3
Durham, T.4
Evans, C.5
Lindroos, C.6
Barrus, S.7
Mathews, D.8
Barnes, M.9
Ratjen, F.10
-
27
-
-
79952211728
-
Denufosol improves lung function in adolescent CF patients
-
abstract
-
Moss RB, Schaberg A, Deans C, Tian W, Smiley L, Herje N. Denufosol improves lung function in adolescent CF patients [abstract]. J Cyst Fibros 2010;9:S20.
-
(2010)
J Cyst Fibros
, vol.9
-
-
Moss, R.B.1
Schaberg, A.2
Deans, C.3
Tian, W.4
Smiley, L.5
Herje, N.6
-
28
-
-
79952215282
-
Aerosol and pharmacokinetic properties of denufosol support its use for early intervention in CF lung disease
-
abstract
-
Navratil T, Evans C, Schaberg A, Johnson F, Durham T, Ren CL, Ratjen F, Moss RB, Accurso FJ. Aerosol and pharmacokinetic properties of denufosol support its use for early intervention in CF lung disease [abstract]. J Cyst Fibros 2010;9:S21.
-
(2010)
J Cyst Fibros
, vol.9
-
-
Navratil, T.1
Evans, C.2
Schaberg, A.3
Johnson, F.4
Durham, T.5
Ren, C.L.6
Ratjen, F.7
Moss, R.B.8
Accurso, F.J.9
-
29
-
-
79952224315
-
Potential of denufosol as an early intervention in CF lung disease: Efficacy in patients with minimal pharmacotherapy in a US phase 3 clinical trial
-
Accurso FJ, Tian W, Schaberg A, Navratil T, Howenstine MS, Liou TG. Potential of denufosol as an early intervention in CF lung disease: efficacy in patients with minimal pharmacotherapy in a US phase 3 clinical trial. J Cyst Fibros 2010;9:S21.
-
(2010)
J Cyst Fibros
, vol.9
-
-
Accurso, F.J.1
Tian, W.2
Schaberg, A.3
Navratil, T.4
Howenstine, M.S.5
Liou, T.G.6
-
30
-
-
28844487754
-
-
Cystic Fibrosis Foundation Bethesda, MD: Cystic Fibrosis Foundation
-
Cystic Fibrosis Foundation. Patient Registry 2004 Annual Data Report. Bethesda, MD: Cystic Fibrosis Foundation; 2005.
-
(2005)
Patient Registry 2004 Annual Data Report
-
-
-
31
-
-
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, Morris EM, Nash ML, Ramsey BW, Rosenstein BJ, Smith AL, Wohl ME; Pulmozyme Study Group. Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. 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
-
32
-
-
30944466084
-
A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis
-
DOI 10.1056/NEJMoa043900
-
Elkins MR, Robinson M, Rose BR, Harbour C, Moriarty CP, Marks GB, Belousova EG, Xuan W, Bye PT. A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. N Engl J Med 2006;354:229-240. (Pubitemid 43113028)
-
(2006)
New England Journal of Medicine
, vol.354
, Issue.3
, 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.P.9
-
33
-
-
0034821607
-
Defining a pulmonary exacerbation in cystic fibrosis
-
DOI 10.1067/mpd.2001.117288
-
Rosenfeld M, Emerson J, Williams-Warren J, Pepe M, Smith A, Montgomery AB, Ramsey B. Defining a pulmonary exacerbation in cystic fibrosis. J Pediatr 2001;139:359-365. (Pubitemid 32889511)
-
(2001)
Journal of Pediatrics
, vol.139
, Issue.3
, pp. 359-365
-
-
Rosenfeld, M.1
Emerson, J.2
Williams-Warren, J.3
Pepe, M.4
Smith, A.5
Montgomery, A.B.6
Ramsey, B.7
-
34
-
-
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;41:161-165. (Pubitemid 27066337)
-
(1997)
Pediatric Research
, vol.41
, Issue.2
, pp. 161-165
-
-
Davis, P.B.1
Byard, P.J.2
Konstan, M.W.3
-
35
-
-
0027551290
-
Pulmonary function between 6 and 18 years of age
-
Wang X, Dockery DW, Wypij D, Fay ME, Ferris BG Jr. Pulmonary function between 6 and 18 years of age. Pediatr Pulmonol 1993;15:75-88.
-
(1993)
Pediatr Pulmonol
, vol.15
, pp. 75-88
-
-
Wang, X.1
Dockery, D.W.2
Wypij, D.3
Fay, M.E.4
Ferris Jr., B.G.5
-
37
-
-
38849129311
-
Reference ranges for spirometry across all ages: A new approach
-
DOI 10.1164/rccm.200708-1248OC
-
Stanojevic S, Wade A, Stocks J, Hankinson J, Coates AL, Pan H, Rosenthal M, Corey M, Lebecque P, Cole TJ. Reference ranges for spirometry across all ages. 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
-
38
-
-
0141816759
-
Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: A randomized controlled trial
-
Macrolide Study Group
-
Saiman L, Marshall BC, Mayer-Hamblett N, Burns JL, Quittner AL, Cibene DA, Coquillette S, Fieberg AY, Accurso FJ, Campbell PW III, et al.; Macrolide Study Group. 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 III, P.W.10
-
39
-
-
77951887288
-
Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: A randomized controlled trial
-
Saiman L, Anstead A, Mayer-Hamblett N, Lands LC, Kloster M, Hocevar-Trnka J, Goss CH, Rose LM, Burns JL, Marshall BC, et al. Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: a randomized controlled trial. JAMA 2010;303:1707-1715.
-
(2010)
JAMA
, vol.303
, pp. 1707-1715
-
-
Saiman, L.1
Anstead, A.2
Mayer-Hamblett, N.3
Lands, L.C.4
Kloster, M.5
Hocevar-Trnka, J.6
Goss, C.H.7
Rose, L.M.8
Burns, J.L.9
Marshall, B.C.10
-
40
-
-
34447530328
-
Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis
-
Scientific Advisory Group and the Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis
-
Konstan MW, Morgan WJ, Butler SM, Pasta DJ, Craib ML, Silva SJ, Stokes DC, Wohl ME, Wagener JS, Regelmann WE, et al.; Scientific Advisory Group and the Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis. J Pediatr 2007;151:134-139.
-
(2007)
J Pediatr
, vol.151
, pp. 134-139
-
-
Konstan, M.W.1
Morgan, W.J.2
Butler, S.M.3
Pasta, D.J.4
Craib, M.L.5
Silva, S.J.6
Stokes, D.C.7
Wohl, M.E.8
Wagener, J.S.9
Regelmann, W.E.10
-
43
-
-
77957694293
-
Failure to recover to baseline pulmonary function after cystic fibrosis pulmonary exacerbation
-
Sanders DB, Bittner RC, Rosenfeld M, Hoffman LR, Redding GJ, Goss CH. Failure to recover to baseline pulmonary function after cystic fibrosis pulmonary exacerbation. Am J Respir Crit Care Med 2010;182:627-632.
-
(2010)
Am J Respir Crit Care Med
, vol.182
, pp. 627-632
-
-
Sanders, D.B.1
Bittner, R.C.2
Rosenfeld, M.3
Hoffman, L.R.4
Redding, G.J.5
Goss, C.H.6
-
44
-
-
79952753579
-
Pulmonary exacerbations are associated with subsequent FEV1 decline in both adults and children with cystic fibrosis
-
In press
-
Sanders DB, Bittner RC, Rosenfeld M, Redding GJ, Goss CM. Pulmonary exacerbations are associated with subsequent FEV1 decline in both adults and children with cystic fibrosis. Pediatr Pulmonol (In press)
-
Pediatr Pulmonol
-
-
Sanders, D.B.1
Bittner, R.C.2
Rosenfeld, M.3
Redding, G.J.4
Goss, C.M.5
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