-
3
-
-
0017198208
-
The lung in cystic fibrosis: A quantitative study including prevalence of pathologic findings among different age groups
-
Bedrossian CW, Greenberg SD, Singer DB, Hansen JJ, Rosenberg HS. The lung in cystic fibrosis: a quantitative study including prevalence of pathologic findings among different age groups. Hum Pathol 1976;7:195-204.
-
(1976)
Hum Pathol
, vol.7
, pp. 195-204
-
-
Bedrossian, C.W.1
Greenberg, S.D.2
Singer, D.B.3
Hansen, J.J.4
Rosenberg, H.S.5
-
4
-
-
0020082418
-
Quantitative evaluation of the development of tracheal submucosal glands in infants with cystic fibrosis and control infants
-
Sturgess J, Imrie J. Quantitative evaluation of the development of tracheal submucosal glands in infants with cystic fibrosis and control infants. Am J Pathol 1982;106:303-311.
-
(1982)
Am J Pathol
, vol.106
, pp. 303-311
-
-
Sturgess, J.1
Imrie, J.2
-
6
-
-
84956707544
-
Airway acidification initiates host defense abnormalities in cystic fibrosis mice
-
Shah VS, Meyerholz DK, Tang XX, Reznikov L, Abou Alaiwa M, Ernst SE, Karp PH, Wohlford-Lenane CL, Heilmann KP, Leidinger MR, et al. Airway acidification initiates host defense abnormalities in cystic fibrosis mice. Science 2016;351:503-507.
-
(2016)
Science
, vol.351
, pp. 503-507
-
-
Shah, V.S.1
Meyerholz, D.K.2
Tang, X.X.3
Reznikov, L.4
Abou Alaiwa, M.5
Ernst, S.E.6
Karp, P.H.7
Wohlford-Lenane, C.L.8
Heilmann, K.P.9
Leidinger, M.R.10
-
7
-
-
84906089250
-
Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis
-
Hoegger MJ, Fischer AJ, McMenimen JD, Ostedgaard LS, Tucker AJ, Awadalla MA, Moninger TO, Michalski AS, Hoffman EA, Zabner J, et al. Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis. Science 2014;345:818-822.
-
(2014)
Science
, vol.345
, pp. 818-822
-
-
Hoegger, M.J.1
Fischer, A.J.2
McMenimen, J.D.3
Ostedgaard, L.S.4
Tucker, A.J.5
Awadalla, M.A.6
Moninger, T.O.7
Michalski, A.S.8
Hoffman, E.A.9
Zabner, J.10
-
8
-
-
67650712233
-
Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening
-
Sly PD, Brennan S, Gangell C, de Klerk N, Murray C, Mott L, Stick SM, Robinson PJ, Robertson CF, Ranganathan SC; 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
-
9
-
-
30344450116
-
High-resolution computed tomography imaging of airway disease in infants with cystic fibrosis
-
Martínez TM, Llapur CJ, Williams TH, Coates C, Gunderman R, Cohen MD, Howenstine MS, Saba O, Coxson HO, Tepper RS. High-resolution computed tomography imaging of airway disease in infants with cystic fibrosis. Am J Respir Crit Care Med 2005;172:1133-1138.
-
(2005)
Am J Respir Crit Care Med
, vol.172
, pp. 1133-1138
-
-
Martínez, T.M.1
Llapur, C.J.2
Williams, T.H.3
Coates, C.4
Gunderman, R.5
Cohen, M.D.6
Howenstine, M.S.7
Saba, O.8
Coxson, H.O.9
Tepper, R.S.10
-
10
-
-
70349831005
-
Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening
-
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. Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening. J Pediatr 2009;155:623-6288.e1.
-
(2009)
J Pediatr
, vol.155
, pp. 623-6288e1
-
-
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
-
11
-
-
0035830289
-
Airway function in infants newly diagnosed with cystic fibrosis
-
Ranganathan SC, Dezateux C, Bush A, Carr SB, Castle RA, Madge S, Price J, Stroobant J, Wade A, Wallis C, et al.; London Collaborative Cystic Fibrosis Group. Airway function in infants newly diagnosed with cystic fibrosis. Lancet 2001;358:1964-1965.
-
(2001)
Lancet
, vol.358
, pp. 1964-1965
-
-
Ranganathan, S.C.1
Dezateux, C.2
Bush, A.3
Carr, S.B.4
Castle, R.A.5
Madge, S.6
Price, J.7
Stroobant, J.8
Wade, A.9
Wallis, C.10
-
12
-
-
11144355490
-
The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis
-
Ranganathan SC, Stocks J, Dezateux C, Bush A, Wade A, Carr S, Castle R, Dinwiddie R, Hoo AF, Lum S, et al. The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis. Am J Respir Crit Care Med 2004;169:928-933.
-
(2004)
Am J Respir Crit Care Med
, vol.169
, pp. 928-933
-
-
Ranganathan, S.C.1
Stocks, J.2
Dezateux, C.3
Bush, A.4
Wade, A.5
Carr, S.6
Castle, R.7
Dinwiddie, R.8
Hoo, A.F.9
Lum, S.10
-
13
-
-
57149116921
-
Lung function in infants with cystic fibrosis diagnosed by newborn screening
-
AREST-CF
-
Linnane BM, Hall GL, Nolan G, Brennan S, Stick SM, Sly PD, Robertson CF, Robinson PJ, Franklin PJ, Turner SW, et al.; 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
-
14
-
-
0030768159
-
Lower airway inflammation in infants and young children with cystic fibrosis
-
Armstrong DS, Grimwood K, Carlin JB, Carzino R, Gutièrrez JP, Hull J, Olinsky A, Phelan EM, Robertson CF, Phelan PD. 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
Carzino, R.4
Gutièrrez, J.P.5
Hull, J.6
Olinsky, A.7
Phelan, E.M.8
Robertson, C.F.9
Phelan, P.D.10
-
15
-
-
0028914085
-
Early pulmonary inflammation in infants with cystic fibrosis
-
Khan TZ, Wagener JS, Bost T, Martinez J, Accurso FJ, Riches DW. Early pulmonary inflammation in infants with cystic fibrosis. Am J Respir Crit Care Med 1995;151:1075-1082.
-
(1995)
Am J Respir Crit Care Med
, vol.151
, pp. 1075-1082
-
-
Khan, T.Z.1
Wagener, J.S.2
Bost, T.3
Martinez, J.4
Accurso, F.J.5
Riches, D.W.6
-
16
-
-
80051572617
-
Infection, inflammation, and lung function decline in infants with cystic fibrosis
-
Australian Respiratory Early Surveillance Team for Cystic Fibrosis AREST CF
-
Pillarisetti N, Williamson E, Linnane B, Skoric B, Robertson CF, Robinson P, Massie J, Hall GL, Sly P, Stick S, et al.; Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST CF). Infection, inflammation, and lung function decline in infants with cystic fibrosis. Am J Respir Crit Care Med 2011;184:75-81.
-
(2011)
Am J Respir Crit Care Med
, vol.184
, pp. 75-81
-
-
Pillarisetti, N.1
Williamson, E.2
Linnane, B.3
Skoric, B.4
Robertson, C.F.5
Robinson, P.6
Massie, J.7
Hall, G.L.8
Sly, P.9
Stick, S.10
-
17
-
-
84866070431
-
Lung function is abnormal in 3-month-old infants with cystic fibrosis diagnosed by newborn screening
-
Hoo AF, Thia LP, Nguyen TT, Bush A, Chudleigh J, Lum S, Ahmed D, Balfour Lynn I, Carr SB, Chavasse RJ, et al.; London Cystic Fibrosis Collaboration. Lung function is abnormal in 3-month-old infants with cystic fibrosis diagnosed by newborn screening. Thorax 2012;67:874-881.
-
(2012)
Thorax
, vol.67
, pp. 874-881
-
-
Hoo, A.F.1
Thia, L.P.2
Nguyen, T.T.3
Bush, A.4
Chudleigh, J.5
Lum, S.6
Ahmed, D.7
Balfour Lynn, I.8
Carr, S.B.9
Chavasse, R.J.10
-
18
-
-
84951064471
-
Cystic fibrosis in young children: A review of disease manifestation, progression, and response to early treatment
-
Van Devanter DR, Kahle JS, O'Sullivan AK, Sikirica S, Hodgkins PS. Cystic fibrosis in young children: a review of disease manifestation, progression, and response to early treatment. J Cyst Fibros 2016;15:147-157.
-
(2016)
J Cyst Fibros
, vol.15
, pp. 147-157
-
-
Van Devanter, D.R.1
Kahle, J.S.2
O'Sullivan, A.K.3
Sikirica, S.4
Hodgkins, P.S.5
-
19
-
-
84942416048
-
Evolution of cystic fibrosis lung function in the early years
-
Bush A, Sly PD. Evolution of cystic fibrosis lung function in the early years. Curr Opin Pulm Med 2015;21:602-608.
-
(2015)
Curr Opin Pulm Med
, vol.21
, pp. 602-608
-
-
Bush, A.1
Sly, P.D.2
-
20
-
-
0029010510
-
Lower respiratory infection and inflammation in infants with newly diagnosed cystic fibrosis
-
Armstrong DS, Grimwood K, Carzino R, Carlin JB, Olinsky A, Phelan PD. Lower respiratory infection and inflammation in infants with newly diagnosed cystic fibrosis. BMJ 1995;310:1571-1572.
-
(1995)
BMJ
, vol.310
, pp. 1571-1572
-
-
Armstrong, D.S.1
Grimwood, K.2
Carzino, R.3
Carlin, J.B.4
Olinsky, A.5
Phelan, P.D.6
-
21
-
-
84894892301
-
Airway inflammation is present by 4 months in CF infants diagnosed on newborn screening
-
Thursfield RM, Bush A, Alton EW, Davies JC. Airway inflammation is present by 4 months in CF infants diagnosed on newborn screening. Pediatr Pulmonol 2012;47:352.
-
(2012)
Pediatr Pulmonol
, vol.47
, pp. 352
-
-
Thursfield, R.M.1
Bush, A.2
Alton, E.W.3
Davies, J.C.4
-
22
-
-
79955005042
-
Evolution of pulmonary inflammation and nutritional status in infants and young children with cystic fibrosis
-
Ranganathan SC, Parsons F, Gangell C, Brennan S, Stick SM, Sly PD; Australian Respiratory Early Surveillance Team for Cystic Fibrosis. Evolution of pulmonary inflammation and nutritional status in infants and young children with cystic fibrosis. Thorax 2011;66:408-413.
-
(2011)
Thorax
, vol.66
, pp. 408-413
-
-
Ranganathan, S.C.1
Parsons, F.2
Gangell, C.3
Brennan, S.4
Stick, S.M.5
Sly, P.D.6
-
23
-
-
80052014087
-
Inflammatory responses to individual microorganisms in the lungs of children with cystic fibrosis
-
AREST CF
-
Gangell C, Gard S, Douglas T, Park J, de Klerk N, Keil T, Brennan S, Ranganathan S, Robins-Browne R, Sly PD; AREST CF. Inflammatory responses to individual microorganisms in the lungs of children with cystic fibrosis. Clin Infect Dis 2011;53:425-432.
-
(2011)
Clin Infect Dis
, vol.53
, pp. 425-432
-
-
Gangell, C.1
Gard, S.2
Douglas, T.3
Park, J.4
De Klerk, N.5
Keil, T.6
Brennan, S.7
Ranganathan, S.8
Robins-Browne, R.9
Sly, P.D.10
-
24
-
-
84862776813
-
Progression of early structural lung disease in young children with cystic fibrosis assessed using CT
-
AREST CF
-
Mott LS, Park J, Murray CP, Gangell CL, de Klerk NH, Robinson PJ, Robertson CF, Ranganathan SC, Sly PD, Stick SM; AREST CF. Progression of early structural lung disease in young children with cystic fibrosis assessed using CT. Thorax 2012;67:509-516.
-
(2012)
Thorax
, vol.67
, pp. 509-516
-
-
Mott, L.S.1
Park, J.2
Murray, C.P.3
Gangell, C.L.4
De Klerk, N.H.5
Robinson, P.J.6
Robertson, C.F.7
Ranganathan, S.C.8
Sly, P.D.9
Stick, S.M.10
-
25
-
-
13544260495
-
Correlation of forced oscillation technique in preschool children with cystic fibrosis with pulmonary inflammation
-
Brennan S, Hall GL, Horak F, Moeller A, Pitrez PM, Franzmann A, Turner S, de Klerk N, Franklin P, Winfield KR, et al. Correlation of forced oscillation technique in preschool children with cystic fibrosis with pulmonary inflammation. Thorax 2005;60:159-163.
-
(2005)
Thorax
, vol.60
, pp. 159-163
-
-
Brennan, S.1
Hall, G.L.2
Horak, F.3
Moeller, A.4
Pitrez, P.M.5
Franzmann, A.6
Turner, S.7
De Klerk, N.8
Franklin, P.9
Winfield, K.R.10
-
26
-
-
84903830061
-
Oxidation contributes to low glutathione in the airways of children with cystic fibrosis
-
AREST CF Investigators
-
Kettle AJ, Turner R, Gangell CL, Harwood DT, Khalilova IS, Chapman AL, Winterbourn CC, Sly PD; AREST CF Investigators. Oxidation contributes to low glutathione in the airways of children with cystic fibrosis. Eur Respir J 2014;44:122-129.
-
(2014)
Eur Respir J
, vol.44
, pp. 122-129
-
-
Kettle, A.J.1
Turner, R.2
Gangell, C.L.3
Harwood, D.T.4
Khalilova, I.S.5
Chapman, A.L.6
Winterbourn, C.C.7
Sly, P.D.8
-
27
-
-
84878000440
-
Risk factors for bronchiectasis in children with cystic fibrosis
-
AREST CF Investigators
-
Sly PD, Gangell CL, Chen L, Ware RS, Ranganathan S, Mott LS, Murray CP, Stick SM; AREST CF Investigators. 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
-
28
-
-
84937631483
-
Inflammation in cystic fibrosis lung disease: Pathogenesis and therapy
-
Cantin AM, Hartl D, Konstan MW, Chmiel JF. Inflammation in cystic fibrosis lung disease: pathogenesis and therapy. J Cyst Fibros 2015;14:419-430.
-
(2015)
J Cyst Fibros
, vol.14
, pp. 419-430
-
-
Cantin, A.M.1
Hartl, D.2
Konstan, M.W.3
Chmiel, J.F.4
-
29
-
-
0036320272
-
Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis
-
Emerson J, Rosenfeld M, McNamara S, Ramsey B, Gibson RL. Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis. Pediatr Pulmonol 2002;34:91-100.
-
(2002)
Pediatr Pulmonol
, vol.34
, pp. 91-100
-
-
Emerson, J.1
Rosenfeld, M.2
McNamara, S.3
Ramsey, B.4
Gibson, R.L.5
-
30
-
-
59649123905
-
Acquisition and eradication of P. Aeruginosa in young children with cystic fibrosis
-
Douglas TA, Brennan S, Gard S, Berry L, Gangell C, Stick SM, Clements BS, Sly PD. Acquisition and eradication of P. aeruginosa in young children with cystic fibrosis. Eur Respir J 2009;33:305-311.
-
(2009)
Eur Respir J
, vol.33
, pp. 305-311
-
-
Douglas, T.A.1
Brennan, S.2
Gard, S.3
Berry, L.4
Gangell, C.5
Stick, S.M.6
Clements, B.S.7
Sly, P.D.8
-
31
-
-
84902477603
-
Differential geographical risk of initial Pseudomonas aeruginosa acquisition in young US children with cystic fibrosis
-
Psoter KJ, Rosenfeld M, De Roos AJ, Mayer JD, Wakefield J. Differential geographical risk of initial Pseudomonas aeruginosa acquisition in young US children with cystic fibrosis. Am J Epidemiol 2014;179:1503-1513.
-
(2014)
Am J Epidemiol
, vol.179
, pp. 1503-1513
-
-
Psoter, K.J.1
Rosenfeld, M.2
De Roos, A.J.3
Mayer, J.D.4
Wakefield, J.5
-
32
-
-
84880898187
-
Geographical differences in first acquisition of Pseudomonas aeruginosa in cystic fibrosis
-
Ranganathan SC, Skoric B, Ramsay KA, Carzino R, Gibson AM, Hart E, Harrison J, Bell SC, Kidd TJ; Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST-CF). Geographical differences in first acquisition of Pseudomonas aeruginosa in cystic fibrosis. Ann Am Thorac Soc 2013;10:108-114.
-
(2013)
Ann Am Thorac Soc
, vol.10
, pp. 108-114
-
-
Ranganathan, S.C.1
Skoric, B.2
Ramsay, K.A.3
Carzino, R.4
Gibson, A.M.5
Hart, E.6
Harrison, J.7
Bell, S.C.8
Kidd, T.J.9
-
33
-
-
84943744505
-
Association of meteorological and geographical factors and risk of initial Pseudomonas aeruginosa acquisition in young children with cystic fibrosis
-
Psoter KJ, De Roos AJ, Wakefield J, Mayer JD, Bryan M, Rosenfeld M. Association of meteorological and geographical factors and risk of initial Pseudomonas aeruginosa acquisition in young children with cystic fibrosis. Epidemiol Infect 2016;155:1075-1083.
-
(2016)
Epidemiol Infect
, vol.155
, pp. 1075-1083
-
-
Psoter, K.J.1
De Roos, A.J.2
Wakefield, J.3
Mayer, J.D.4
Bryan, M.5
Rosenfeld, M.6
-
34
-
-
84961289926
-
Fine particulate matter exposure and initial Pseudomonas aeruginosa acquisition in cystic fibrosis
-
Psoter KJ, De Roos AJ, Mayer JD, Kaufman JD, Wakefield J, Rosenfeld M. Fine particulate matter exposure and initial Pseudomonas aeruginosa acquisition in cystic fibrosis. Ann Am Thorac Soc 2015;12:385-391.
-
(2015)
Ann Am Thorac Soc
, vol.12
, pp. 385-391
-
-
Psoter, K.J.1
De Roos, A.J.2
Mayer, J.D.3
Kaufman, J.D.4
Wakefield, J.5
Rosenfeld, M.6
-
35
-
-
84937516045
-
Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-years
-
ACFBAL Study Investigators
-
Kidd TJ, Ramsay KA, Vidmar S, Carlin JB, Bell SC, Wainwright CE, Grimwood K, ACFBAL Study Investigators. Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-years. J Cyst Fibros 2015;14:361-369.
-
(2015)
J Cyst Fibros
, vol.14
, pp. 361-369
-
-
Kidd, T.J.1
Ramsay, K.A.2
Vidmar, S.3
Carlin, J.B.4
Bell, S.C.5
Wainwright, C.E.6
Grimwood, K.7
-
36
-
-
0030995361
-
Antibiotic treatment of initial colonization with Pseudomonas aeruginosa postpones chronic infection and prevents deterioration of pulmonary function in cystic fibrosis
-
Frederiksen B, Koch C, Høiby N. Antibiotic treatment of initial colonization with Pseudomonas aeruginosa postpones chronic infection and prevents deterioration of pulmonary function in cystic fibrosis. Pediatr Pulmonol 1997;23:330-335.
-
(1997)
Pediatr Pulmonol
, vol.23
, pp. 330-335
-
-
Frederiksen, B.1
Koch, C.2
Høiby, N.3
-
37
-
-
84926130841
-
Serology as a diagnostic tool for predicting initial Pseudomonas aeruginosa acquisition in children with cystic fibrosis
-
EPIC Investigators
-
Daines C, Van De Vanter D, Khan U, Emerson J, Heltshe S, McNamara S, Anstead M, Langkamp M, Doring G, Ratjen F, et al.; EPIC Investigators. Serology as a diagnostic tool for predicting initial Pseudomonas aeruginosa acquisition in children with cystic fibrosis. J Cyst Fibros 2014;13:542-549.
-
(2014)
J Cyst Fibros
, vol.13
, pp. 542-549
-
-
Daines, C.1
Van De Vanter, D.2
Khan, U.3
Emerson, J.4
Heltshe, S.5
McNamara, S.6
Anstead, M.7
Langkamp, M.8
Doring, G.9
Ratjen, F.10
-
38
-
-
78149361309
-
Value of serology in predicting Pseudomonas aeruginosa infection in young children with cystic fibrosis
-
members of AREST CF and ACFBAL Trial
-
Douglas TA, Brennan S, Berry L, Winfield K, Wainwright CE, Grimwood K, Stick SM, Sly PD; members of AREST CF and ACFBAL Trial. Value of serology in predicting Pseudomonas aeruginosa infection in young children with cystic fibrosis. Thorax 2010;65:985-990.
-
(2010)
Thorax
, vol.65
, pp. 985-990
-
-
Douglas, T.A.1
Brennan, S.2
Berry, L.3
Winfield, K.4
Wainwright, C.E.5
Grimwood, K.6
Stick, S.M.7
Sly, P.D.8
-
39
-
-
79960151730
-
Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: A randomized trial
-
ACFBAL Study Investigators
-
Wainwright CE, Vidmar S, Armstrong DS, Byrnes CA, Carlin JB, Cheney J, Cooper PJ, Grimwood K, Moodie M, Robertson CF, et al.; ACFBAL Study Investigators. 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
-
40
-
-
46349106358
-
Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis
-
London Cystic Fibrosis Collaboration
-
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.
-
(2008)
Am J Respir Crit Care Med
, vol.178
, 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
-
41
-
-
84923930953
-
Early respiratory infection is associated with reduced spirometry in children with cystic fibrosis
-
AREST CF
-
Ramsey KA, Ranganathan S, Park J, Skoric B, Adams AM, Simpson SJ, Robins-Browne RM, Franklin PJ, de Klerk NH, Sly PD, et al.; AREST CF. Early respiratory infection is associated with reduced spirometry in children with cystic fibrosis. Am J Respir Crit Care Med 2014;190:1111-1116.
-
(2014)
Am J Respir Crit Care Med
, vol.190
, pp. 1111-1116
-
-
Ramsey, K.A.1
Ranganathan, S.2
Park, J.3
Skoric, B.4
Adams, A.M.5
Simpson, S.J.6
Robins-Browne, R.M.7
Franklin, P.J.8
De Klerk, N.H.9
Sly, P.D.10
-
42
-
-
84979097475
-
Development of the nasopharyngeal microbiota in infants with cystic fibrosis
-
Prevaes SM, de Winter-de Groot KM, Janssens HM, de Steenhuijsen Piters WA, Tramper-Stranders GA, Wyllie AL, Hasrat R, Tiddens HA, van Westreenen M, van der Ent CK, et al. Development of the nasopharyngeal microbiota in infants with cystic fibrosis. Am J Respir Crit Care Med 2016;193:504-515.
-
(2016)
Am J Respir Crit Care Med
, vol.193
, pp. 504-515
-
-
Prevaes, S.M.1
De Winter-De Groot, K.M.2
Janssens, H.M.3
De Steenhuijsen Piters, W.A.4
Tramper-Stranders, G.A.5
Wyllie, A.L.6
Hasrat, R.7
Tiddens, H.A.8
Van Westreenen, M.9
Van Der Ent, C.K.10
-
43
-
-
84966691911
-
The nasal microbiota in infants with cystic fibrosis in the first year of life: A prospective cohort study
-
Mika M, Korten I, Qi W, Regamey N, Frey U, Casaulta C, Latzin P, Hilty M; SCILD study group. The nasal microbiota in infants with cystic fibrosis in the first year of life: a prospective cohort study. Lancet Respir Med 2016;4:627-635.
-
(2016)
Lancet Respir Med
, vol.4
, pp. 627-635
-
-
Mika, M.1
Korten, I.2
Qi, W.3
Regamey, N.4
Frey, U.5
Casaulta, C.6
Latzin, P.7
Hilty, M.8
-
44
-
-
85021078785
-
The lower airway microbiota in early cystic fibrosis lung disease: A longitudinal analysis
-
online ahead of print 9 Mar
-
Frayman KB, Armstrong DS, Carzino R, Ferkol T, Grimwood K, Storch GA, Teo SM, Wylie KM, Ranganathan SC. The lower airway microbiota in early cystic fibrosis lung disease: a longitudinal analysis. Thorax [online ahead of print] 9 Mar. 2017; DOI: 10.1136/thoraxjnl-2016-209279.
-
(2017)
Thorax
-
-
Frayman, K.B.1
Armstrong, D.S.2
Carzino, R.3
Ferkol, T.4
Grimwood, K.5
Storch, G.A.6
Teo, S.M.7
Wylie, K.M.8
Ranganathan, S.C.9
-
45
-
-
1542377466
-
Early morphologic changes in the lungs of asymptomatic infants and young children with cystic fibrosis
-
Brody AS. Early morphologic changes in the lungs of asymptomatic infants and young children with cystic fibrosis. J Pediatr 2004;144:145-146.
-
(2004)
J Pediatr
, vol.144
, pp. 145-146
-
-
Brody, A.S.1
-
46
-
-
84878716092
-
Novel end points for clinical trials in young children with cystic fibrosis
-
Simpson SJ, Mott LS, Esther CR Jr, Stick SM, Hall GL. Novel end points for clinical trials in young children with cystic fibrosis. Expert Rev Respir Med 2013;7:231-243.
-
(2013)
Expert Rev Respir Med
, vol.7
, pp. 231-243
-
-
Simpson, S.J.1
Mott, L.S.2
Esther, C.R.3
Stick, S.M.4
Hall, G.L.5
-
47
-
-
84883506964
-
Chest computed tomography: A validated surrogate endpoint of cystic fibrosis lung disease?
-
Loeve M, Krestin GP, Rosenfeld M, de Bruijne M, Stick SM, Tiddens HA. Chest computed tomography: a validated surrogate endpoint of cystic fibrosis lung disease? Eur Respir J 2013;42:844-857.
-
(2013)
Eur Respir J
, vol.42
, pp. 844-857
-
-
Loeve, M.1
Krestin, G.P.2
Rosenfeld, M.3
De Bruijne, M.4
Stick, S.M.5
Tiddens, H.A.6
-
48
-
-
67649476123
-
Bronchiectasis in an asymptomatic infant with cystic fibrosis diagnosed following newborn screening
-
Mott LS, Gangell CL, Murray CP, Stick SM, Sly PD, Arest CF. Bronchiectasis in an asymptomatic infant with cystic fibrosis diagnosed following newborn screening. J Cyst Fibros 2009;8:285-857.
-
(2009)
J Cyst Fibros
, vol.8
, pp. 285-857
-
-
Mott, L.S.1
Gangell, C.L.2
Murray, C.P.3
Stick, S.M.4
Sly, P.D.5
Arest, C.F.6
-
49
-
-
39049084491
-
Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis
-
Gustafsson PM, De Jong PA, Tiddens HA, Lindblad A. Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis. Thorax 2008;63:129-134.
-
(2008)
Thorax
, vol.63
, pp. 129-134
-
-
Gustafsson, P.M.1
De Jong, P.A.2
Tiddens, H.A.3
Lindblad, A.4
-
50
-
-
79956360940
-
Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF
-
Owens CM, Aurora P, Stanojevic S, Bush A, Wade A, Oliver C, Calder A, Price J, Carr SB, Shankar A, et al.; London Cystic Fibrosis Collaboration. Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF. Thorax 2011;66:481-488.
-
(2011)
Thorax
, vol.66
, pp. 481-488
-
-
Owens, C.M.1
Aurora, P.2
Stanojevic, S.3
Bush, A.4
Wade, A.5
Oliver, C.6
Calder, A.7
Price, J.8
Carr, S.B.9
Shankar, A.10
-
51
-
-
0034868951
-
Lung function testing in infants with cystic fibrosis: Lessons from the past and future directions
-
Gappa M, Ranganathan SC, Stocks J. Lung function testing in infants with cystic fibrosis: lessons from the past and future directions. Pediatr Pulmonol 2001;32:228-245.
-
(2001)
Pediatr Pulmonol
, vol.32
, pp. 228-245
-
-
Gappa, M.1
Ranganathan, S.C.2
Stocks, J.3
-
52
-
-
0014531389
-
Ventilatory function in infants with cystic fibrosis: Physiological assessment of halation therapy
-
Phelan PD, Gracey M, Williams HE, Anderson CM. Ventilatory function in infants with cystic fibrosis: physiological assessment of halation therapy. Arch Dis Child 1969;44:393-400.
-
(1969)
Arch Dis Child
, vol.44
, pp. 393-400
-
-
Phelan, P.D.1
Gracey, M.2
Williams, H.E.3
Anderson, C.M.4
-
53
-
-
80051850244
-
Air trapping on chest CT is associated with worse ventilation distribution in infants with cystic fibrosis diagnosed following newborn screening
-
AREST CF Investigators
-
Hall GL, Logie KM, Parsons F, Schulzke SM, Nolan G, Murray C, Ranganathan S, Robinson P, Sly PD, Stick SM, et al.; AREST CF Investigators. Air trapping on chest CT is associated with worse ventilation distribution in infants with cystic fibrosis diagnosed following newborn screening. PLoS One 2011;6:e23932.
-
(2011)
PLoS One
, vol.6
, pp. e23932
-
-
Hall, G.L.1
Logie, K.M.2
Parsons, F.3
Schulzke, S.M.4
Nolan, G.5
Murray, C.6
Ranganathan, S.7
Robinson, P.8
Sly, P.D.9
Stick, S.M.10
-
54
-
-
85021069579
-
Endexpiratory lung volume is not associated with gas trapping on CT in early cystic fibrosis lung disease [abstract]
-
Rosenow TM, Mok C, Ramsay KA, Murray C, Hall GL, Stick SM. Endexpiratory lung volume is not associated with gas trapping on CT in early cystic fibrosis lung disease [abstract]. Am J Respir Crit Care Med 2016;193:A5591.
-
(2016)
Am J Respir Crit Care Med
, vol.193
, pp. A5591
-
-
Rosenow, T.M.1
Mok, C.2
Ramsay, K.A.3
Murray, C.4
Hall, G.L.5
Stick, S.M.6
-
55
-
-
84898994097
-
Magnetic resonance imaging detects changes in structure and perfusion, and response to therapy in early cystic fibrosis lung disease
-
Wielpütz MO, Puderbach M, Kopp-Schneider A, Stahl M, Fritzsching E, Sommerburg O, Ley S, Sumkauskaite M, Biederer J, Kauczor HU, et al. Magnetic resonance imaging detects changes in structure and perfusion, and response to therapy in early cystic fibrosis lung disease. Am J Respir Crit Care Med 2014;189:956-965.
-
(2014)
Am J Respir Crit Care Med
, vol.189
, pp. 956-965
-
-
Wielpütz, M.O.1
Puderbach, M.2
Kopp-Schneider, A.3
Stahl, M.4
Fritzsching, E.5
Sommerburg, O.6
Ley, S.7
Sumkauskaite, M.8
Biederer, J.9
Kauczor, H.U.10
-
56
-
-
84890445863
-
Air trapping and airflow obstruction in newborn cystic fibrosis piglets
-
Adam RJ, Michalski AS, Bauer C, Abou Alaiwa MH, Gross TJ, Awadalla MS, Bouzek DC, Gansemer ND, Taft PJ, Hoegger MJ, et al. Air trapping and airflow obstruction in newborn cystic fibrosis piglets. Am J Respir Crit Care Med 2013;188:1434-1441.
-
(2013)
Am J Respir Crit Care Med
, vol.188
, pp. 1434-1441
-
-
Adam, R.J.1
Michalski, A.S.2
Bauer, C.3
Abou Alaiwa, M.H.4
Gross, T.J.5
Awadalla, M.S.6
Bouzek, D.C.7
Gansemer, N.D.8
Taft, P.J.9
Hoegger, M.J.10
-
57
-
-
84938501003
-
PRAGMA-CF: A quantitative structural lung disease computed tomography outcome in young children with cystic fibrosis
-
Rosenow T, Oudraad MC, Murray CP, Turkovic L, Kuo W, de Bruijne M, Ranganathan SC, Tiddens HA, Stick SM; Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST CF). PRAGMA-CF: a quantitative structural lung disease computed tomography outcome in young children with cystic fibrosis. Am J Respir Crit Care Med 2015;191:1158-1165.
-
(2015)
Am J Respir Crit Care Med
, vol.191
, pp. 1158-1165
-
-
Rosenow, T.1
Oudraad, M.C.2
Murray, C.P.3
Turkovic, L.4
Kuo, W.5
De Bruijne, M.6
Ranganathan, S.C.7
Tiddens, H.A.8
Stick, S.M.9
-
58
-
-
84860110054
-
Early cystic fibrosis lung disease detected by bronchoalveolar lavage and lung clearance index
-
Belessis Y, Dixon B, Hawkins G, Pereira J, Peat J, MacDonald R, Field P, Numa A, Morton J, Lui K, et al. Early cystic fibrosis lung disease detected by bronchoalveolar lavage and lung clearance index. Am J Respir Crit Care Med 2012;185:862-873.
-
(2012)
Am J Respir Crit Care Med
, vol.185
, pp. 862-873
-
-
Belessis, Y.1
Dixon, B.2
Hawkins, G.3
Pereira, J.4
Peat, J.5
MacDonald, R.6
Field, P.7
Numa, A.8
Morton, J.9
Lui, K.10
-
59
-
-
84948971137
-
Progressive ventilation inhomogeneity in infants with cystic fibrosis after pulmonary infection
-
AREST CF
-
Simpson SJ, Ranganathan S, Park J, Turkovic L, Robins-Browne RM, Skoric B, Ramsey KA, Rosenow T, Banton GL, Berry L, et al.; AREST CF. Progressive ventilation inhomogeneity in infants with cystic fibrosis after pulmonary infection. Eur Respir J 2015;46:1680-1690.
-
(2015)
Eur Respir J
, vol.46
, pp. 1680-1690
-
-
Simpson, S.J.1
Ranganathan, S.2
Park, J.3
Turkovic, L.4
Robins-Browne, R.M.5
Skoric, B.6
Ramsey, K.A.7
Rosenow, T.8
Banton, G.L.9
Berry, L.10
-
60
-
-
84973409422
-
Lung clearance index and structural lung disease on computed tomography in early cystic fibrosis
-
AREST CF
-
Ramsey KA, Rosenow T, Turkovic L, Skoric B, Banton G, Adams AM, Simpson SJ, Murray C, Ranganathan SC, Stick SM, et al.; AREST CF. Lung clearance index and structural lung disease on computed tomography in early cystic fibrosis. Am J Respir Crit Care Med 2016;193:60-67.
-
(2016)
Am J Respir Crit Care Med
, vol.193
, pp. 60-67
-
-
Ramsey, K.A.1
Rosenow, T.2
Turkovic, L.3
Skoric, B.4
Banton, G.5
Adams, A.M.6
Simpson, S.J.7
Murray, C.8
Ranganathan, S.C.9
Stick, S.M.10
-
61
-
-
84899046260
-
Cystic fibrosis: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases
-
Pittman JE, Cutting G, Davis SD, Ferkol T, Boucher R. Cystic fibrosis: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases. Ann Am Thorac Soc 2014;11:S161-S168.
-
(2014)
Ann Am Thorac Soc
, vol.11
, pp. S161-S168
-
-
Pittman, J.E.1
Cutting, G.2
Davis, S.D.3
Ferkol, T.4
Boucher, R.5
-
62
-
-
80051566309
-
Exciting new clinical trials in cystic fibrosis: Infants need not apply
-
Stick SM, Sly PD. Exciting new clinical trials in cystic fibrosis: infants need not apply. Am J Respir Crit Care Med 2011;183:1577-1578.
-
(2011)
Am J Respir Crit Care Med
, vol.183
, pp. 1577-1578
-
-
Stick, S.M.1
Sly, P.D.2
-
63
-
-
84950129551
-
Parental experience of information and education processes following diagnosis of their infant with cystic fibrosis via newborn screening
-
AREST-CF
-
Jessup M, Douglas T, Priddis L, Branch-Smith C, Shields L, Arest CF; AREST-CF. Parental experience of information and education processes following diagnosis of their infant with cystic fibrosis via newborn screening. J Pediatr Nurs 2016;31:e233-e241.
-
(2016)
J Pediatr Nurs
, vol.31
, pp. e233-e241
-
-
Jessup, M.1
Douglas, T.2
Priddis, L.3
Branch-Smith, C.4
Shields, L.5
Arest, C.F.6
-
64
-
-
84905732526
-
What do parents experience and how do they cope with the AREST-CF early surveillance program for infants and children with cystic fibrosis?
-
ARESTCF
-
Branch-Smith C, Pooley J, Shields L, Stick S, Douglas T; ARESTCF. What do parents experience and how do they cope with the AREST-CF early surveillance program for infants and children with cystic fibrosis? J Cyst Fibros 2013;12:S3.
-
(2013)
J Cyst Fibros
, vol.12
, pp. S3
-
-
Branch-Smith, C.1
Pooley, J.2
Shields, L.3
Stick, S.4
Douglas, T.5
-
65
-
-
77951887288
-
Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: A randomized controlled trial
-
Saiman L, Anstead M, Mayer-Hamblett N, Lands LC, Kloster M, Hocevar-Trnka J, Goss CH, Rose LM, Burns JL, Marshall BC, et al.; AZ0004 Azithromycin Study Group. 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, M.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
-
66
-
-
0032718969
-
Diagnostic accuracy of oropharyngeal cultures in infants and young children with cystic fibrosis
-
Rosenfeld M, Emerson J, Accurso F, Armstrong D, Castile R, Grimwood K, Hiatt P, McCoy K, McNamara S, Ramsey B, et al. Diagnostic accuracy of oropharyngeal cultures in infants and young children with cystic fibrosis. Pediatr Pulmonol 1999;28:321-328.
-
(1999)
Pediatr Pulmonol
, vol.28
, pp. 321-328
-
-
Rosenfeld, M.1
Emerson, J.2
Accurso, F.3
Armstrong, D.4
Castile, R.5
Grimwood, K.6
Hiatt, P.7
McCoy, K.8
McNamara, S.9
Ramsey, B.10
-
67
-
-
84866143187
-
Prevalence of cystic fibrosis pathogens in the oropharynx of healthy children and implications for cystic fibrosis care
-
Rosenfeld M, Bernardo-Ocampo C, Emerson J, Genatossio A, Burns J, Gibson R. Prevalence of cystic fibrosis pathogens in the oropharynx of healthy children and implications for cystic fibrosis care. J Cyst Fibros 2012;11:456-457.
-
(2012)
J Cyst Fibros
, vol.11
, pp. 456-457
-
-
Rosenfeld, M.1
Bernardo-Ocampo, C.2
Emerson, J.3
Genatossio, A.4
Burns, J.5
Gibson, R.6
-
68
-
-
33947155711
-
Infant care patterns at epidemiologic study of cystic fibrosis sites that achieve superior childhood lung function
-
Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis
-
Padman R, McColley SA, Miller DP, Konstan MW, Morgan WJ, Schechter MS, Ren CL, Wagener JS; Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Infant care patterns at epidemiologic study of cystic fibrosis sites that achieve superior childhood lung function. Pediatrics 2007;119:e531-e537.
-
(2007)
Pediatrics
, vol.119
, pp. e531-e537
-
-
Padman, R.1
McColley, S.A.2
Miller, D.P.3
Konstan, M.W.4
Morgan, W.J.5
Schechter, M.S.6
Ren, C.L.7
Wagener, J.S.8
-
69
-
-
10344250594
-
Effect of treatment with dornase alpha on airway inflammation in patients with cystic fibrosis
-
Paul K, Rietschel E, Ballmann M, Griese M, Worlitzsch D, Shute J, Chen C, Schink T, Döring G, van Koningsbruggen S, et al.; Bronchoalveolar Lavage for the Evaluation of Antiinflammatory Treatment Study Group. Effect of treatment with dornase alpha on airway inflammation in patients with cystic fibrosis. Am J Respir Crit Care Med 2004;169:719-725.
-
(2004)
Am J Respir Crit Care Med
, vol.169
, pp. 719-725
-
-
Paul, K.1
Rietschel, E.2
Ballmann, M.3
Griese, M.4
Worlitzsch, D.5
Shute, J.6
Chen, C.7
Schink, T.8
Döring, G.9
Van Koningsbruggen, S.10
-
70
-
-
0035666058
-
A two-year randomized, placebocontrolled trial of dornase alfa in young patients with cystic fibrosis with mild lung function abnormalities
-
Quan JM, Tiddens HA, Sy JP, McKenzie SG, Montgomery MD, Robinson PJ, Wohl ME, Konstan MW; Pulmozyme Early Intervention Trial Study Group. A two-year randomized, placebocontrolled 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
-
71
-
-
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
-
72
-
-
79953287790
-
The effect of dornase alfa on ventilation inhomogeneity in patients with cystic fibrosis
-
Amin R, Subbarao P, Lou W, Jabar A, Balkovec S, Jensen R, Kerrigan S, Gustafsson P, Ratjen F. The effect of dornase alfa on ventilation inhomogeneity in patients with cystic fibrosis. Eur Respir J 2011;37:806-812.
-
(2011)
Eur Respir J
, vol.37
, pp. 806-812
-
-
Amin, R.1
Subbarao, P.2
Lou, W.3
Jabar, A.4
Balkovec, S.5
Jensen, R.6
Kerrigan, S.7
Gustafsson, P.8
Ratjen, F.9
-
73
-
-
0035021689
-
Use of computerized tomography and chest x-rays in evaluating efficacy of aerosolized recombinant human DNase in cystic fibrosis patients younger than age 5 years: A preliminary study
-
Nasr SZ, Kuhns LR, Brown RW, Hurwitz ME, Sanders GM, Strouse PJ. Use of computerized tomography and chest x-rays in evaluating efficacy of aerosolized recombinant human DNase in cystic fibrosis patients younger than age 5 years: a preliminary study. Pediatr Pulmonol 2001;31:377-382.
-
(2001)
Pediatr Pulmonol
, vol.31
, pp. 377-382
-
-
Nasr, S.Z.1
Kuhns, L.R.2
Brown, R.W.3
Hurwitz, M.E.4
Sanders, G.M.5
Strouse, P.J.6
-
74
-
-
61549124077
-
Recovery of birth weight z score within 2 years of diagnosis is positively associated with pulmonary status at 6 years of age in children with cystic fibrosis
-
Wisconsin Cystic Fibrosis Neonatal Screening G
-
Lai HJ, Shoff SM, Farrell PM, Wisconsin Cystic Fibrosis Neonatal Screening G; Wisconsin Cystic Fibrosis Neonatal Screening Group. Recovery of birth weight z score within 2 years of diagnosis is positively associated with pulmonary status at 6 years of age in children with cystic fibrosis. Pediatrics 2009;123:714-722.
-
(2009)
Pediatrics
, vol.123
, pp. 714-722
-
-
Lai, H.J.1
Shoff, S.M.2
Farrell, P.M.3
-
75
-
-
85052907527
-
Vitamin D deficiency is associated with increased risk of lower respiratory infection with S. Aureus among infants & preschool children with CF [abstract]
-
Douglas T, Park J, Ranganathan S, Hart E, Carzino R, Skoric B, Garratt L, Ebdon A, Sly PD, Stick S. Vitamin D deficiency is associated with increased risk of lower respiratory infection with S. aureus among infants & preschool children with CF [abstract]. Pediatr Pulmonol 2012;47:A264.
-
(2012)
Pediatr Pulmonol
, vol.47
, pp. A264
-
-
Douglas, T.1
Park, J.2
Ranganathan, S.3
Hart, E.4
Carzino, R.5
Skoric, B.6
Garratt, L.7
Ebdon, A.8
Sly, P.D.9
Stick, S.10
-
77
-
-
10344219968
-
Renal impairment in cystic fibrosis patients due to repeated intravenous aminoglycoside use
-
Al-Aloul M, Miller H, Alapati S, Stockton PA, Ledson MJ, Walshaw MJ. Renal impairment in cystic fibrosis patients due to repeated intravenous aminoglycoside use. Pediatr Pulmonol 2005;39:15-20.
-
(2005)
Pediatr Pulmonol
, vol.39
, pp. 15-20
-
-
Al-Aloul, M.1
Miller, H.2
Alapati, S.3
Stockton, P.A.4
Ledson, M.J.5
Walshaw, M.J.6
-
78
-
-
84875451063
-
Understanding the costs of care for cystic fibrosis: An analysis by age and health state
-
van Gool K, Norman R, Delatycki MB, Hall J, Massie J. Understanding the costs of care for cystic fibrosis: an analysis by age and health state. Value Health 2013;16:345-355.
-
(2013)
Value Health
, vol.16
, pp. 345-355
-
-
Van Gool, K.1
Norman, R.2
Delatycki, M.B.3
Hall, J.4
Massie, J.5
-
79
-
-
85021078832
-
-
accessed 2016 Jun. 1
-
Queensland Children's Medical Research Institute. Prevention of bronchiectasis in infants with CF; 2016 [accessed 2016 Jun. 1]. Available from: https://clinicaltrials.gov/ct2/show/NCT01270074
-
(2016)
Prevention of Bronchiectasis in Infants with CF
-
-
-
80
-
-
85021082648
-
-
accessed 2016 Jun. 1
-
CF Therapeutics Development Network Coordinating Center. Inhaled study of inhaled saline in cystic fibrosis; 2016 [accessed 2016 Jun. 1]. Available from: https://clinicaltrials.gov/ct2/show/NCT00709280
-
(2016)
Inhaled Study of Inhaled Saline in Cystic Fibrosis
-
-
-
82
-
-
84880040035
-
Early intervention studies in infants and preschool children with cystic fibrosis: Are we ready?
-
Stick S, Tiddens H, Aurora P, Gustafsson P, Ranganathan S, Robinson P, Rosenfeld M, Sly P, Ratjen F. Early intervention studies in infants and preschool children with cystic fibrosis: are we ready? Eur Respir J 2013;42:527-538.
-
(2013)
Eur Respir J
, vol.42
, pp. 527-538
-
-
Stick, S.1
Tiddens, H.2
Aurora, P.3
Gustafsson, P.4
Ranganathan, S.5
Robinson, P.6
Rosenfeld, M.7
Sly, P.8
Ratjen, F.9
-
83
-
-
84948972128
-
Reply: Excess risk of cancer from computed tomography scan is small but not so low as to be incalculable
-
Rosenow T, Oudraad MC, Murray CP, Turkovic L, Kuo W, de Bruijne M, Ranganathan SC, Tiddens HA, Stick SM. Reply: excess risk of cancer from computed tomography scan is small but not so low as to be incalculable. Am J Respir Crit Care Med 2015;192:1397-1399.
-
(2015)
Am J Respir Crit Care Med
, vol.192
, pp. 1397-1399
-
-
Rosenow, T.1
Oudraad, M.C.2
Murray, C.P.3
Turkovic, L.4
Kuo, W.5
De Bruijne, M.6
Ranganathan, S.C.7
Tiddens, H.A.8
Stick, S.M.9
-
84
-
-
84901747416
-
Monitoring cystic fibrosis lung disease by computed tomography: Radiation risk in perspective
-
Kuo W, Ciet P, Tiddens HA, Zhang W, Guillerman RP, van Straten M. Monitoring cystic fibrosis lung disease by computed tomography: radiation risk in perspective. Am J Respir Crit Care Med 2014;189:1328-1336.
-
(2014)
Am J Respir Crit Care Med
, vol.189
, pp. 1328-1336
-
-
Kuo, W.1
Ciet, P.2
Tiddens, H.A.3
Zhang, W.4
Guillerman, R.P.5
Van Straten, M.6
-
85
-
-
85006105563
-
Metabolomic biomarkers predictive of early structural lung disease in cystic fibrosis
-
AREST CF
-
Esther CR Jr, Turkovic L, Rosenow T, Muhlebach MS, Boucher RC, Ranganathan S, Stick SM; AREST CF. Metabolomic biomarkers predictive of early structural lung disease in cystic fibrosis. Eur Respir J 2016;48:1612-1621.
-
(2016)
Eur Respir J
, vol.48
, pp. 1612-1621
-
-
Esther, C.R.1
Turkovic, L.2
Rosenow, T.3
Muhlebach, M.S.4
Boucher, R.C.5
Ranganathan, S.6
Stick, S.M.7
-
86
-
-
84877054679
-
Magnetic resonance imaging of cystic fibrosis lung disease
-
Wielpütz MO, Eichinger M, Puderbach M. Magnetic resonance imaging of cystic fibrosis lung disease. J Thorac Imaging 2013;28:151-159.
-
(2013)
J Thorac Imaging
, vol.28
, pp. 151-159
-
-
Wielpütz, M.O.1
Eichinger, M.2
Puderbach, M.3
-
87
-
-
84957971675
-
Assessment of CF lung disease using motion corrected PROPELLER MRI: A comparison with CT
-
Ciet P, Serra G, Bertolo S, Spronk S, Ros M, Fraioli F, Quattrucci S, Assael MB, Catalano C, Pomerri F, et al. Assessment of CF lung disease using motion corrected PROPELLER MRI: a comparison with CT. Eur Radiol 2016;26:780-787.
-
(2016)
Eur Radiol
, vol.26
, pp. 780-787
-
-
Ciet, P.1
Serra, G.2
Bertolo, S.3
Spronk, S.4
Ros, M.5
Fraioli, F.6
Quattrucci, S.7
Assael, M.B.8
Catalano, C.9
Pomerri, F.10
-
88
-
-
84941087623
-
Respiratory tract exacerbations revisited: Ventilation, inflammation, perfusion, and structure (VIPS) monitoring to redefine treatment
-
Tiddens HA, Stick SM, Wild JM, Ciet P, Parker GJ, Koch A, Vogel-Claussen J. Respiratory tract exacerbations revisited: ventilation, inflammation, perfusion, and structure (VIPS) monitoring to redefine treatment. Pediatr Pulmonol 2015;50:S57-S65.
-
(2015)
Pediatr Pulmonol
, vol.50
, pp. S57-S65
-
-
Tiddens, H.A.1
Stick, S.M.2
Wild, J.M.3
Ciet, P.4
Parker, G.J.5
Koch, A.6
Vogel-Claussen, J.7
|