-
2
-
-
77949678705
-
-
Cystic Fibrosis Foundation. Cystic Fibrosis Foundation, Bethesda, MD
-
Cystic Fibrosis Foundation. 2008. Patient registry: annual data report 2008. Cystic Fibrosis Foundation, Bethesda, MD.
-
(2008)
Patient Registry: Annual Data Report 2008
-
-
-
3
-
-
0033773012
-
Antibiotic therapy against Pseudomonas aeruginosa in cystic fibrosis: A European consensus
-
Doring G, Conway SP, Heijerman HG, Hodson ME, Høiby N, Smyth A, Touw DJ. 2000. Antibiotic therapy against Pseudomonas aeruginosa in cystic fibrosis: a European consensus. Eur. Respir. J. 16:749-767. http://dx.doi.org/ 10.1034/j.1399-3003.2000.16d30.x.
-
(2000)
Eur. Respir. J.
, vol.16
, pp. 749-767
-
-
Doring, G.1
Conway, S.P.2
Heijerman, H.G.3
Hodson, M.E.4
Høiby, N.5
Smyth, A.6
Touw, D.J.7
-
4
-
-
0036320272
-
Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis
-
DOI 10.1002/ppul.10127
-
Emerson J, Rosenfeld M, McNamara S, Ramsey B, Gibson RL. 2002. Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis. Pediatr. Pulmonol. 34:91-100. http://dx.doi.org/10.1002/ppul.10127. (Pubitemid 34809519)
-
(2002)
Pediatric Pulmonology
, vol.34
, Issue.2
, pp. 91-100
-
-
Emerson, J.1
Rosenfeld, M.2
McNamara, S.3
Ramsey, B.4
Gibson, R.L.5
-
5
-
-
0026831341
-
Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis
-
Henry RL, Mellis CM, Petrovic L. 1992. Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis. Pediatr. Pulmonol. 12:158-161. http://dx.doi.org/10.1002/ppul.1950120306.
-
(1992)
Pediatr. Pulmonol.
, vol.12
, pp. 158-161
-
-
Henry, R.L.1
Mellis, C.M.2
Petrovic, L.3
-
6
-
-
84906083713
-
-
Novartis Pharmaceuticals Corporation, East Hanover, NJ
-
Novartis. 2013. Tobi (tobramycin inhalation solution). package insert. Novartis Pharmaceuticals Corporation, East Hanover, NJ. https://www.pharma.us. novartis.com/product/pi/pdf/tobi.pdf.
-
(2013)
Tobi (Tobramycin Inhalation Solution). Package Insert
-
-
-
8
-
-
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, Geller D, Wagner MH, Quittner AL. 2006. A multi-method assessment of treatment adherence for children with cystic fibrosis. J. Cyst. Fibros. 5:177-185. http://dx.doi.org/10.1016/j.jcf.2006.03. 002. (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
-
9
-
-
70349084570
-
Pharmacokinetic and pharmacodynamic evaluation of liposomal amikacin for inhalation in cystic fibrosis patients with chronic pseudomonal infection
-
Okusanya OO, Bhavnani SM, Hammel JP, Minic P, Dupont LJ, Forrest A, Mulder GJ, Mackinson C, Ambrose PG, Gupta R. 2009. Pharmacokinetic and pharmacodynamic evaluation of liposomal amikacin for inhalation in cystic fibrosis patients with chronic pseudomonal infection. Antimicrob. Agents Chemother. 53:3847-3854. http://dx.doi.org/10.1128/AAC.00872-08.
-
(2009)
Antimicrob. Agents Chemother.
, vol.53
, pp. 3847-3854
-
-
Okusanya, O.O.1
Bhavnani, S.M.2
Hammel, J.P.3
Minic, P.4
Dupont, L.J.5
Forrest, A.6
Mulder, G.J.7
Mackinson, C.8
Ambrose, P.G.9
Gupta, R.10
-
10
-
-
84881542878
-
Phase II studies of nebulised Arikace in CF patients with Pseudomonas aeruginosa infection
-
Arikace Study Group
-
Clancy JP, Dupont L, Konstan MW, Billings J, Fustik S, Goss CH, Lymp J, Minic P, Quittner AL, Rubenstein RC, Young KR, Saiman L, Burns JL, Govan JRW, Ramsey B, Gupta R, Arikace Study Group. 2013. Phase II studies of nebulised Arikace in CF patients with Pseudomonas aeruginosa infection. Thorax 68:818-825. http://dx.doi.org/10.1136/thoraxjnl-2012-202230.
-
(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
Young, K.R.11
Saiman, L.12
Burns, J.L.13
Govan, J.R.W.14
Ramsey, B.15
Gupta, R.16
-
12
-
-
0035216180
-
Ways to fit a PK model with some data below the quantification limit
-
DOI 10.1023/A:1012299115260
-
Beal SL. 2001. Ways to fit a PK model with some data below the quantification limit. J. Pharmacokinet. Pharmacodyn. 28:481-504. http://dx.doi.org/10.1023/A:1012299115260. (Pubitemid 33151426)
-
(2001)
Journal of Pharmacokinetics and Pharmacodynamics
, vol.28
, Issue.5
, pp. 481-504
-
-
Beal, S.L.1
-
14
-
-
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, Gellar DE. 2011. Safety, efficacy and convenience of tobramycin inhalation powder in cystic fibrosis patients: the EAGER trial. J. Cyst. Fibros. 10:54-61. http://dx.doi.org/10.1016/j.jcf.2010.10.003.
-
(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
Gellar, D.E.10
-
15
-
-
65949124667
-
Efficacy and safety of inhaled aztreonam lysine for airway Pseudomonas in cystic fibrosis
-
Retsch-Bogart GA, Quittner AL, Gibson RL, Oermann CM, McCoy KS, Montgomery AB, Cooper PJ. 2009. Efficacy and safety of inhaled aztreonam lysine for airway Pseudomonas in cystic fibrosis. Chest 135:1223-1232. http://dx.doi.org/10.1378/chest.08-1421.
-
(2009)
Chest
, vol.135
, pp. 1223-1232
-
-
Retsch-Bogart, G.A.1
Quittner, A.L.2
Gibson, R.L.3
Oermann, C.M.4
McCoy, K.S.5
Montgomery, A.B.6
Cooper, P.J.7
-
16
-
-
84875842391
-
Inhaled aztreonam lysine vs. Inhaled tobramycin in cystic fibrosis: A comparative efficacy trial
-
AZLI Active Comparator Study Group
-
Assael BM, Pressler T, Bilton D, Fayon M, Fischer R, Chiron R, Larosa M, Knoop C, McElvaney N, Lewis SA, Bresnik M, Montgomery AB, Oermann CM, AZLI Active Comparator Study Group. 2013. Inhaled aztreonam lysine vs. inhaled tobramycin in cystic fibrosis: a comparative efficacy trial. J. Cyst. Fibros. 12:130-140. http://dx.doi.org/10.1016/j.jcf.2012.07.006.
-
(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
Bresnik, M.11
Montgomery, A.B.12
Oermann, C.M.13
-
17
-
-
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. 2010. An 18-month study of the safety and efficacy of repeated courses of inhaled aztreonam lysine in cystic fibrosis. Pediatr. Pulmonol. 45:1121-1134. http://dx.doi.org/10.1002/ppul.21301.
-
(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
|