-
1
-
-
79957946294
-
Managing cystic fibrosis: Strategies that increase life expectancy and improve quality of life
-
Cohen-Cymberknoh M, Shoseyov D, Kerem E,. Managing cystic fibrosis: strategies that increase life expectancy and improve quality of life. Am. J. Respir. Crit. Care Med. 2011; 183: 1463-1471.
-
(2011)
Am. J. Respir. Crit. Care Med.
, vol.183
, pp. 1463-1471
-
-
Cohen-Cymberknoh, M.1
Shoseyov, D.2
Kerem, E.3
-
2
-
-
84891904005
-
Factors associated with FEV1 decline in cystic fibrosis: Analysis of the ECFS patient registry
-
et al
-
Kerem E, Viviani L, Zolin A, MacNeill S, Hatziagorou E, Ellemunter H, Drevinek P, Gulmans V, Krivec U, Olesen H, et al. Factors associated with FEV1 decline in cystic fibrosis: analysis of the ECFS patient registry. Eur. Respir. J. 2014; 43: 125-133.
-
(2014)
Eur. Respir. J.
, vol.43
, pp. 125-133
-
-
Kerem, E.1
Viviani, L.2
Zolin, A.3
MacNeill, S.4
Hatziagorou, E.5
Ellemunter, H.6
Drevinek, P.7
Gulmans, V.8
Krivec, U.9
Olesen, H.10
-
3
-
-
84869120178
-
Treatment of lung infection in patients with cystic fibrosis: Current and future strategies
-
Consensus Study G
-
Doring G, Flume P, Heijerman H, Elborn JS, Consensus Study G. Treatment of lung infection in patients with cystic fibrosis: current and future strategies. J. Cyst. Fibros. 2012; 11: 461-479.
-
(2012)
J. Cyst. Fibros.
, vol.11
, pp. 461-479
-
-
Doring, G.1
Flume, P.2
Heijerman, H.3
Elborn, J.S.4
-
4
-
-
70350446684
-
Cystic fibrosis pulmonary guidelines: Treatment of pulmonary exacerbations
-
Clinical Practice Guidelines for Pulmonary Therapies C
-
Flume PA, Mogayzel PJ Jr, Robinson KA, Goss CH, Rosenblatt RL, Kuhn RJ, Marshall BC, Clinical Practice Guidelines for Pulmonary Therapies C. Cystic fibrosis pulmonary guidelines: treatment of pulmonary exacerbations. Am. J. Respir. Crit. Care Med. 2009; 180: 802-808.
-
(2009)
Am. J. Respir. Crit. Care Med.
, vol.180
, pp. 802-808
-
-
Flume, P.A.1
Mogayzel, P.J.2
Robinson, K.A.3
Goss, C.H.4
Rosenblatt, R.L.5
Kuhn, R.J.6
Marshall, B.C.7
-
5
-
-
84863448941
-
Transmissible strains of Pseudomonas aeruginosa in cystic fibrosis lung infections
-
Fothergill JL, Walshaw MJ, Winstanley C,. Transmissible strains of Pseudomonas aeruginosa in cystic fibrosis lung infections. Eur. Respir. J. 2012; 40: 227-238.
-
(2012)
Eur. Respir. J.
, vol.40
, pp. 227-238
-
-
Fothergill, J.L.1
Walshaw, M.J.2
Winstanley, C.3
-
6
-
-
0023923679
-
A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto
-
Corey M, McLaughlin FJ, Williams M, Levison H,. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J. Clin. Epidemiol. 1988; 41: 583-591.
-
(1988)
J. Clin. Epidemiol.
, vol.41
, pp. 583-591
-
-
Corey, M.1
McLaughlin, F.J.2
Williams, M.3
Levison, H.4
-
7
-
-
84869083220
-
An overview of international literature from cystic fibrosis registries. Part 4: Update 2011
-
et al
-
Salvatore D, Buzzetti R, Baldo E, Furnari ML, Lucidi V, Manunza D, Marinelli I, Messore B, Neri AS, Raia V, et al. An overview of international literature from cystic fibrosis registries. Part 4: update 2011. J. Cyst. Fibros. 2012; 11: 480-493.
-
(2012)
J. Cyst. Fibros.
, vol.11
, pp. 480-493
-
-
Salvatore, D.1
Buzzetti, R.2
Baldo, E.3
Furnari, M.L.4
Lucidi, V.5
Manunza, D.6
Marinelli, I.7
Messore, B.8
Neri, A.S.9
Raia, V.10
-
8
-
-
84896511421
-
Key findings of the US Cystic Fibrosis Foundation's clinical practice benchmarking project
-
Boyle MP, Sabadosa KA, Quinton HB, Marshall BC, Schechter MS,. Key findings of the US Cystic Fibrosis Foundation's clinical practice benchmarking project. BMJ Qual. Saf. 2014; 23 (Suppl. 1): i15-22.
-
(2014)
BMJ Qual. Saf.
, vol.23
, pp. i15-i22
-
-
Boyle, M.P.1
Sabadosa, K.A.2
Quinton, H.B.3
Marshall, B.C.4
Schechter, M.S.5
-
9
-
-
84877098245
-
Shared Pseudomonas aeruginosa genotypes are common in Australian cystic fibrosis centres
-
et al
-
Kidd TJ, Ramsay KA, Hu H, Marks GB, Wainwright CE, Bye PT, Elkins MR, Robinson PJ, Rose BR, Wilson JW, et al. Shared Pseudomonas aeruginosa genotypes are common in Australian cystic fibrosis centres. Eur. Respir. J. 2013; 41: 1091-1100.
-
(2013)
Eur. Respir. J.
, vol.41
, pp. 1091-1100
-
-
Kidd, T.J.1
Ramsay, K.A.2
Hu, H.3
Marks, G.B.4
Wainwright, C.E.5
Bye, P.T.6
Elkins, M.R.7
Robinson, P.J.8
Rose, B.R.9
Wilson, J.W.10
-
11
-
-
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, B.G.5
-
13
-
-
70349555987
-
2000 CDC Growth Charts for the United States: Methods and development
-
Kuczmarski RJ, Ogden CL, Guo SS, Grummer-Strawn LM, Flegal KM, Mei Z, Wei R, Curtin LR, Roche AF, Johnson CL,. 2000 CDC Growth Charts for the United States: methods and development. Vital Health Stat. 11 2002; 246: 1-190.
-
(2002)
Vital Health Stat. 11
, vol.246
, pp. 1-190
-
-
Kuczmarski, R.J.1
Ogden, C.L.2
Guo, S.S.3
Grummer-Strawn, L.M.4
Flegal, K.M.5
Mei, Z.6
Wei, R.7
Curtin, L.R.8
Roche, A.F.9
Johnson, C.L.10
-
14
-
-
0028950532
-
Mixed morphotype testing of Pseudomonas aeruginosa cultures from cystic fibrosis patients
-
Wolter JM, Kotsiou G, McCormack JG,. Mixed morphotype testing of Pseudomonas aeruginosa cultures from cystic fibrosis patients. J. Med. Microbiol. 1995; 42: 220-224.
-
(1995)
J. Med. Microbiol.
, vol.42
, pp. 220-224
-
-
Wolter, J.M.1
Kotsiou, G.2
McCormack, J.G.3
-
16
-
-
77957874402
-
-
Version 1.3: European Committee on Antimicrobial Susceptibility Testing European Committee on Antimicrobial Susceptibility Testing. [Accessed 14 Nov 2014.] Available from URL
-
European Committee on Antimicrobial Susceptibility Testing. Breakpoint tables for interpretation of MICs and Zone Diameters, Version 1.3: European Committee on Antimicrobial Susceptibility Testing; 2011. [Accessed 14 Nov 2014.] Available from URL: http://www.eucast.org/clinical-breakpoints
-
(2011)
Breakpoint Tables for Interpretation of MICs and Zone Diameters
-
-
-
17
-
-
84955368040
-
-
Clinical and Laboratory Standards Institute. Antimicrobial Susceptibility Testing. Wayne, PA, USA: Clinical and Laboratory Standards Institute
-
Clinical and Laboratory Standards Institute. Performance standards for testing: twenty-first informational supplement M100-S21. Antimicrobial Susceptibility Testing. Wayne, PA, USA: Clinical and Laboratory Standards Institute; 2011.
-
(2011)
Performance Standards for Testing: Twenty-first Informational Supplement M100-S21
-
-
-
18
-
-
66149109850
-
Low rates of Pseudomonas aeruginosa misidentification in isolates from cystic fibrosis patients
-
et al
-
Kidd TJ, Ramsay KA, Hu H, Bye PT, Elkins MR, Grimwood K, Harbour C, Marks GB, Nissen MD, Robinson PJ, et al. Low rates of Pseudomonas aeruginosa misidentification in isolates from cystic fibrosis patients. J. Clin. Microbiol. 2009; 47: 1503-1509.
-
(2009)
J. Clin. Microbiol.
, vol.47
, pp. 1503-1509
-
-
Kidd, T.J.1
Ramsay, K.A.2
Hu, H.3
Bye, P.T.4
Elkins, M.R.5
Grimwood, K.6
Harbour, C.7
Marks, G.B.8
Nissen, M.D.9
Robinson, P.J.10
-
19
-
-
0029808250
-
Antibiotic susceptibility of multiply resistant Pseudomonas aeruginosa isolated from patients with cystic fibrosis, including candidates for transplantation
-
Saiman L, Mehar F, Niu WW, Neu HC, Shaw KJ, Miller G, Prince A,. Antibiotic susceptibility of multiply resistant Pseudomonas aeruginosa isolated from patients with cystic fibrosis, including candidates for transplantation. Clin. Infect. Dis. 1996; 23: 532-537.
-
(1996)
Clin. Infect. Dis.
, vol.23
, pp. 532-537
-
-
Saiman, L.1
Mehar, F.2
Niu, W.W.3
Neu, H.C.4
Shaw, K.J.5
Miller, G.6
Prince, A.7
-
20
-
-
34548048797
-
Incidence and risk factors for multiple antibiotic-resistant Pseudomonas aeruginosa in cystic fibrosis
-
Merlo CA, Boyle MP, Diener-West M, Marshall BC, Goss CH, Lechtzin N,. Incidence and risk factors for multiple antibiotic-resistant Pseudomonas aeruginosa in cystic fibrosis. Chest 2007; 132: 562-568.
-
(2007)
Chest
, vol.132
, pp. 562-568
-
-
Merlo, C.A.1
Boyle, M.P.2
Diener-West, M.3
Marshall, B.C.4
Goss, C.H.5
Lechtzin, N.6
-
21
-
-
69049110965
-
Pseudomonas aeruginosa - A phenomenon of bacterial resistance
-
Strateva T, Yordanov D,. Pseudomonas aeruginosa-a phenomenon of bacterial resistance. J. Med. Microbiol. 2009; 58 (Pt 9): 1133-1148.
-
(2009)
J. Med. Microbiol.
, vol.58
, pp. 1133-1148
-
-
Strateva, T.1
Yordanov, D.2
-
22
-
-
0032938913
-
Epidemiology and clinical outcomes of patients with multiresistant Pseudomonas aeruginosa
-
Harris A, Torres-Viera C, Venkataraman L, DeGirolami P, Samore M, Carmeli Y,. Epidemiology and clinical outcomes of patients with multiresistant Pseudomonas aeruginosa. Clin. Infect. Dis. 1999; 28: 1128-1133.
-
(1999)
Clin. Infect. Dis.
, vol.28
, pp. 1128-1133
-
-
Harris, A.1
Torres-Viera, C.2
Venkataraman, L.3
DeGirolami, P.4
Samore, M.5
Carmeli, Y.6
-
23
-
-
84865330965
-
Anaerobic Pseudomonas aeruginosa and other obligately anaerobic bacterial biofilms growing in the thick airway mucus of chronically infected cystic fibrosis patients: An emerging paradigm or "old Hat"?
-
Su S, Hassett DJ,. Anaerobic Pseudomonas aeruginosa and other obligately anaerobic bacterial biofilms growing in the thick airway mucus of chronically infected cystic fibrosis patients: an emerging paradigm or "Old Hat"? Expert Opin. Ther. Targets 2012; 16: 859-873.
-
(2012)
Expert Opin. Ther. Targets
, vol.16
, pp. 859-873
-
-
Su, S.1
Hassett, D.J.2
-
24
-
-
0036167851
-
Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients
-
et al
-
Worlitzsch D, Tarran R, Ulrich M, Schwab U, Cekici A, Meyer KC, Birrer P, Bellon G, Berger J, Weiss T, et al. Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients. J. Clin. Invest. 2002; 109: 317-325.
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 317-325
-
-
Worlitzsch, D.1
Tarran, R.2
Ulrich, M.3
Schwab, U.4
Cekici, A.5
Meyer, K.C.6
Birrer, P.7
Bellon, G.8
Berger, J.9
Weiss, T.10
-
25
-
-
29944446141
-
Multidrug-resistant Pseudomonas aeruginosa: Risk factors and clinical impact
-
Aloush V, Navon-Venezia S, Seigman-Igra Y, Cabili S, Carmeli Y,. Multidrug-resistant Pseudomonas aeruginosa: risk factors and clinical impact. Antimicrob. Agents Chemother. 2006; 50: 43-48.
-
(2006)
Antimicrob. Agents Chemother.
, vol.50
, pp. 43-48
-
-
Aloush, V.1
Navon-Venezia, S.2
Seigman-Igra, Y.3
Cabili, S.4
Carmeli, Y.5
-
26
-
-
0033059706
-
Emergence of antibiotic-resistant Pseudomonas aeruginosa: Comparison of risks associated with different antipseudomonal agents
-
Carmeli Y, Troillet N, Eliopoulos GM, Samore MH,. Emergence of antibiotic-resistant Pseudomonas aeruginosa: comparison of risks associated with different antipseudomonal agents. Antimicrob. Agents Chemother. 1999; 43: 1379-1382.
-
(1999)
Antimicrob. Agents Chemother.
, vol.43
, pp. 1379-1382
-
-
Carmeli, Y.1
Troillet, N.2
Eliopoulos, G.M.3
Samore, M.H.4
-
27
-
-
84862501656
-
Results of antibiotic susceptibility testing do not influence clinical outcome in children with cystic fibrosis
-
Hurley MN, Ariff AH, Bertenshaw C, Bhatt J, Smyth AR,. Results of antibiotic susceptibility testing do not influence clinical outcome in children with cystic fibrosis. J. Cyst. Fibros. 2012; 11: 288-292.
-
(2012)
J. Cyst. Fibros.
, vol.11
, pp. 288-292
-
-
Hurley, M.N.1
Ariff, A.H.2
Bertenshaw, C.3
Bhatt, J.4
Smyth, A.R.5
-
28
-
-
0037541096
-
Susceptibility testing of Pseudomonas aeruginosa isolates and clinical response to parenteral antibiotic administration: Lack of association in cystic fibrosis
-
Smith AL, Fiel SB, Mayer-Hamblett N, Ramsey B, Burns JL,. Susceptibility testing of Pseudomonas aeruginosa isolates and clinical response to parenteral antibiotic administration: lack of association in cystic fibrosis. Chest 2003; 123: 1495-1502.
-
(2003)
Chest
, vol.123
, pp. 1495-1502
-
-
Smith, A.L.1
Fiel, S.B.2
Mayer-Hamblett, N.3
Ramsey, B.4
Burns, J.L.5
-
29
-
-
33644508050
-
Outcomes of adults with cystic fibrosis infected with antibiotic-resistant Pseudomonas aeruginosa
-
Lechtzin N, John M, Irizarry R, Merlo C, Diette GB, Boyle MP,. Outcomes of adults with cystic fibrosis infected with antibiotic-resistant Pseudomonas aeruginosa. Respiration 2006; 73: 27-33.
-
(2006)
Respiration
, vol.73
, pp. 27-33
-
-
Lechtzin, N.1
John, M.2
Irizarry, R.3
Merlo, C.4
Diette, G.B.5
Boyle, M.P.6
-
30
-
-
84862487763
-
Multiple antibiotic-resistant Pseudomonas aeruginosa and lung function decline in patients with cystic fibrosis
-
Scientific Advisory Group I, Coordinators of the Epidemiologic Study of Cystic F
-
Ren CL, Konstan MW, Yegin A, Rasouliyan L, Trzaskoma B, Morgan WJ, Regelmann W, Scientific Advisory Group I, Coordinators of the Epidemiologic Study of Cystic F. Multiple antibiotic-resistant Pseudomonas aeruginosa and lung function decline in patients with cystic fibrosis. J. Cyst. Fibros. 2012; 11: 293-299.
-
(2012)
J. Cyst. Fibros.
, vol.11
, pp. 293-299
-
-
Ren, C.L.1
Konstan, M.W.2
Yegin, A.3
Rasouliyan, L.4
Trzaskoma, B.5
Morgan, W.J.6
Regelmann, W.7
-
31
-
-
0037384154
-
Multiresistant Pseudomonas aeruginosa in a pediatric cystic fibrosis center: Natural history and implications for segregation
-
Davies G, McShane D, Davies JC, Bush A,. Multiresistant Pseudomonas aeruginosa in a pediatric cystic fibrosis center: natural history and implications for segregation. Pediatr. Pulmonol. 2003; 35: 253-256.
-
(2003)
Pediatr. Pulmonol.
, vol.35
, pp. 253-256
-
-
Davies, G.1
McShane, D.2
Davies, J.C.3
Bush, A.4
-
32
-
-
20444477989
-
Antibiotic allergy in cystic fibrosis
-
Parmar JS, Nasser S,. Antibiotic allergy in cystic fibrosis. Thorax 2005; 60: 517-520.
-
(2005)
Thorax
, vol.60
, pp. 517-520
-
-
Parmar, J.S.1
Nasser, S.2
-
33
-
-
77958154266
-
Aminoglycoside use in cystic fibrosis: Therapeutic strategies and toxicity
-
Prayle A, Smyth AR,. Aminoglycoside use in cystic fibrosis: therapeutic strategies and toxicity. Curr. Opin. Pulm. Med. 2010; 16: 604-610.
-
(2010)
Curr. Opin. Pulm. Med.
, vol.16
, pp. 604-610
-
-
Prayle, A.1
Smyth, A.R.2
-
34
-
-
60449117029
-
High treatment burden in adults with cystic fibrosis: Challenges to disease self-management
-
Sawicki GS, Sellers DE, Robinson WM,. High treatment burden in adults with cystic fibrosis: challenges to disease self-management. J. Cyst. Fibros. 2009; 8: 91-96.
-
(2009)
J. Cyst. Fibros.
, vol.8
, pp. 91-96
-
-
Sawicki, G.S.1
Sellers, D.E.2
Robinson, W.M.3
-
35
-
-
84870341542
-
Molecular epidemiology of chronic Pseudomonas aeruginosa airway infections in cystic fibrosis
-
Cramer N, Wiehlmann L, Ciofu O, Tamm S, Hoiby N, Tummler B,. Molecular epidemiology of chronic Pseudomonas aeruginosa airway infections in cystic fibrosis. PLoS ONE 2012; 7: e50731.
-
(2012)
PLoS ONE
, vol.7
, pp. e50731
-
-
Cramer, N.1
Wiehlmann, L.2
Ciofu, O.3
Tamm, S.4
Hoiby, N.5
Tummler, B.6
-
36
-
-
84907734820
-
Pharmacokinetics and pharmacodynamics of aerosolized antibacterial agents in chronically infected cystic fibrosis patients
-
Dalhoff A,. Pharmacokinetics and pharmacodynamics of aerosolized antibacterial agents in chronically infected cystic fibrosis patients. Clin. Microbiol. Rev. 2014; 27: 753-782.
-
(2014)
Clin. Microbiol. Rev.
, vol.27
, pp. 753-782
-
-
Dalhoff, A.1
-
37
-
-
0042922372
-
Laboratory aspects of management of chronic pulmonary infections in patients with cystic fibrosis
-
Miller MB, Gilligan PH,. Laboratory aspects of management of chronic pulmonary infections in patients with cystic fibrosis. J. Clin. Microbiol. 2003; 41: 4009-4015.
-
(2003)
J. Clin. Microbiol.
, vol.41
, pp. 4009-4015
-
-
Miller, M.B.1
Gilligan, P.H.2
-
38
-
-
34249937399
-
Realities of expectorated sputum collection in the pediatric cystic fibrosis clinic
-
Radhakrishnan DK, Corey M, Dell SD,. Realities of expectorated sputum collection in the pediatric cystic fibrosis clinic. Arch. Pediatr. Adolesc. Med. 2007; 161: 603-606.
-
(2007)
Arch. Pediatr. Adolesc. Med.
, vol.161
, pp. 603-606
-
-
Radhakrishnan, D.K.1
Corey, M.2
Dell, S.D.3
-
39
-
-
79960151730
-
Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: A randomized trial
-
et al
-
Wainwright CE, Vidmar S, Armstrong DS, Byrnes CA, Carlin JB, Cheney J, Cooper PJ, Grimwood K, Moodie M, Robertson CF, et al. Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: a randomized trial. JAMA 2011; 306: 163-171.
-
(2011)
JAMA
, vol.306
, pp. 163-171
-
-
Wainwright, C.E.1
Vidmar, S.2
Armstrong, D.S.3
Byrnes, C.A.4
Carlin, J.B.5
Cheney, J.6
Cooper, P.J.7
Grimwood, K.8
Moodie, M.9
Robertson, C.F.10
|