-
1
-
-
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
-
2
-
-
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,. 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
-
3
-
-
70349831005
-
Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening
-
e1.
-
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: 623-628, e1.
-
(2009)
J. Pediatr.
, vol.155
, pp. 623-628
-
-
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
-
4
-
-
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
-
5
-
-
78349237748
-
Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children
-
Meyerholz DK, Stoltz DA, Namati E, Ramachandran S, Pezzulo AA, Smith AR, Rector MV, Suter MJ, Kao S, McLennan G, et-al. Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children. Am. J. Respir. Crit. Care Med. 2010; 182: 1251-1261.
-
(2010)
Am. J. Respir. Crit. Care Med.
, vol.182
, pp. 1251-1261
-
-
Meyerholz, D.K.1
Stoltz, D.A.2
Namati, E.3
Ramachandran, S.4
Pezzulo, A.A.5
Smith, A.R.6
Rector, M.V.7
Suter, M.J.8
Kao, S.9
McLennan, G.10
-
6
-
-
84862776813
-
Progression of early structural lung disease in young children with cystic fibrosis assessed using CT
-
Mott LS, Park J, Murray CP, Gangell CL, de Klerk NH, Robinson PJ, Robertson CF, Ranganathan SC, Sly PD, Stick SM,. 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
-
7
-
-
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
-
8
-
-
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,. 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
-
9
-
-
79960151730
-
Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: A randomized trial
-
Wainwright CE, Vidmar S, Armstrong DS, Byrnes CA, Carlin JB, Cheney J, Cooper PJ, Grimwood K, Moodie M, Robertson CF,. 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
-
10
-
-
80051557744
-
Which test is best: Cystic fibrosis
-
Ranganathan S, Gappa M,. Which test is best: cystic fibrosis. Eur. Respir. Mon. 2010; 47: 225-239.
-
(2010)
Eur. Respir. Mon.
, vol.47
, pp. 225-239
-
-
Ranganathan, S.1
Gappa, M.2
-
11
-
-
30344465311
-
ATS/ERS statement: Raised volume forced expirations in infants: Guidelines for current practice
-
Lum SL, Stocks J, Castile R, Davis S, Henschen M, Jones M, Morris MG, Ranganathan S, Sly P, Tepper RS,. ATS/ERS statement: raised volume forced expirations in infants: guidelines for current practice. Am. J. Respir. Crit. Care Med. 2005; 172: 1463-1471.
-
(2005)
Am. J. Respir. Crit. Care Med.
, vol.172
, pp. 1463-1471
-
-
Lum, S.L.1
Stocks, J.2
Castile, R.3
Davis, S.4
Henschen, M.5
Jones, M.6
Morris, M.G.7
Ranganathan, S.8
Sly, P.9
Tepper, R.S.10
-
12
-
-
0037111312
-
Relative ability of full and partial forced expiratory maneuvers to identify diminished airway function in infants with cystic fibrosis
-
Ranganathan SC, Bush A, Dezateux C, Carr SB, Hoo AF, Lum S, Madge S, Price J, Stroobant J, Wade A, et-al. Relative ability of full and partial forced expiratory maneuvers to identify diminished airway function in infants with cystic fibrosis. Am. J. Respir. Crit. Care Med. 2002; 166: 1350-1357.
-
(2002)
Am. J. Respir. Crit. Care Med.
, vol.166
, pp. 1350-1357
-
-
Ranganathan, S.C.1
Bush, A.2
Dezateux, C.3
Carr, S.B.4
Hoo, A.F.5
Lum, S.6
Madge, S.7
Price, J.8
Stroobant, J.9
Wade, A.10
-
13
-
-
0027988038
-
Improved detection of abnormal respiratory function using forced expiration from raised lung volume in infants with cystic fibrosis
-
Turner DJ, Lanteri CJ, LeSouef PN, Sly PD,. Improved detection of abnormal respiratory function using forced expiration from raised lung volume in infants with cystic fibrosis. Eur. Respir. J. 1994; 7: 1995-1999.
-
(1994)
Eur. Respir. J.
, vol.7
, pp. 1995-1999
-
-
Turner, D.J.1
Lanteri, C.J.2
Lesouef, P.N.3
Sly, P.D.4
-
14
-
-
0014317137
-
Airway closure: Demonstration by breathing 100 percent O2 at low lung volumes and by N2 washout
-
Burger EJ Jr, Macklem P,. Airway closure: demonstration by breathing 100 percent O2 at low lung volumes and by N2 washout. J. Appl. Physiol. 1968; 25: 139-148.
-
(1968)
J. Appl. Physiol.
, vol.25
, pp. 139-148
-
-
Burger, Jr.E.J.1
MacKlem, P.2
-
15
-
-
0037215668
-
Method for assessment of volume of trapped gas in infants during multiple-breath inert gas washout
-
Gustafsson PM, Kallman S, Ljungberg H, Lindblad A,. Method for assessment of volume of trapped gas in infants during multiple-breath inert gas washout. Pediatr. Pulmonol. 2003; 35: 42-49.
-
(2003)
Pediatr. Pulmonol.
, vol.35
, pp. 42-49
-
-
Gustafsson, P.M.1
Kallman, S.2
Ljungberg, H.3
Lindblad, A.4
-
16
-
-
0034094161
-
Moment ratio analysis of multiple breath nitrogen washout in infants with lung disease
-
Schibler A, Schneider M, Frey U, Kraemer R,. Moment ratio analysis of multiple breath nitrogen washout in infants with lung disease. Eur. Respir. J. 2000; 15: 1094-1101.
-
(2000)
Eur. Respir. J.
, vol.15
, pp. 1094-1101
-
-
Schibler, A.1
Schneider, M.2
Frey, U.3
Kraemer, R.4
-
17
-
-
34247167236
-
Early detection of cystic fibrosis lung disease: Multiple-breath washout versus raised volume tests
-
Lum S, Gustafsson P, Ljungberg H, Hulskamp G, Bush A, Carr SB, Castle R, Hoo AF, Price J, Ranganathan S, et-al. Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests. Thorax 2007; 62: 341-347.
-
(2007)
Thorax
, vol.62
, pp. 341-347
-
-
Lum, S.1
Gustafsson, P.2
Ljungberg, H.3
Hulskamp, G.4
Bush, A.5
Carr, S.B.6
Castle, R.7
Hoo, A.F.8
Price, J.9
Ranganathan, S.10
-
18
-
-
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. 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
-
19
-
-
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
-
20
-
-
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. 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
-
21
-
-
57149116921
-
Lung function in infants with cystic fibrosis diagnosed by newborn screening
-
Linnane BM, Hall GL, Nolan G, Brennan S, Stick SM, Sly PD, Robertson CF, Robinson PJ, Franklin PJ, Turner SW, 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
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
-
22
-
-
80051572617
-
Infection, inflammation, and lung function decline in infants with cystic fibrosis
-
Pillarisetti N, Williamson E, Linnane B, Skoric B, Robertson CF, Robinson P, Massie J, Hall GL, Sly P, Stick S, et-al. 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
-
23
-
-
66749185766
-
Association of lower airway inflammation with physiologic findings in young children with cystic fibrosis
-
Peterson-Carmichael SL, Harris WT, Goel R, Noah TL, Johnson R, Leigh MW, Davis SD,. Association of lower airway inflammation with physiologic findings in young children with cystic fibrosis. Pediatr. Pulmonol. 2009; 44: 503-511.
-
(2009)
Pediatr. Pulmonol.
, vol.44
, pp. 503-511
-
-
Peterson-Carmichael, S.L.1
Harris, W.T.2
Goel, R.3
Noah, T.L.4
Johnson, R.5
Leigh, M.W.6
Davis, S.D.7
-
24
-
-
0036789637
-
Early airway infection, inflammation, and lung function in cystic fibrosis
-
Nixon GM, Armstrong DS, Carzino R, Carlin JB, Olinsky A, Robertson CF, Grimwood K, Wainwright C,. 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
Carlin, J.B.4
Olinsky, A.5
Robertson, C.F.6
Grimwood, K.7
Wainwright, C.8
-
25
-
-
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
-
26
-
-
30344450116
-
High-resolution computed tomography imaging of airway disease in infants with cystic fibrosis
-
Martinez 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
-
-
Martinez, 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
-
27
-
-
80051850244
-
Air trapping on chest CT is associated with worse ventilation distribution in infants with cystic fibrosis diagnosed following newborn screening
-
Hall GL, Logie KM, Parsons F, Schulzke SM, Nolan G, Murray C, Ranganathan S, Robinson P, Sly PD, Stick SM, et-al. 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
-
-
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
-
28
-
-
84861892411
-
Inhaled hypertonic saline in infants and children younger than 6 years with cystic fibrosis: The ISIS randomized controlled trial
-
Rosenfeld M, Ratjen F, Brumback L, Daniel S, Rowbotham R, McNamara S, Johnson R, Kronmal R, Davis SD,. Inhaled hypertonic saline in infants and children younger than 6 years with cystic fibrosis: the ISIS randomized controlled trial. JAMA 2012; 307: 2269-2277.
-
(2012)
JAMA
, vol.307
, pp. 2269-2277
-
-
Rosenfeld, M.1
Ratjen, F.2
Brumback, L.3
Daniel, S.4
Rowbotham, R.5
McNamara, S.6
Johnson, R.7
Kronmal, R.8
Davis, S.D.9
-
29
-
-
84882662774
-
Lung clearance index as an outcome measure for clinical trials in young children with cystic fibrosis. A pilot study using inhaled hypertonic saline
-
Subbarao P, Stanojevic S, Brown M, Jensen R, Rosenfeld M, Davis S, Brumback L, Gustafsson P, Ratjen F,. Lung clearance index as an outcome measure for clinical trials in young children with cystic fibrosis. A pilot study using inhaled hypertonic saline. Am. J. Respir. Crit. Care Med. 2013; 188: 456-460.
-
(2013)
Am. J. Respir. Crit. Care Med.
, vol.188
, pp. 456-460
-
-
Subbarao, P.1
Stanojevic, S.2
Brown, M.3
Jensen, R.4
Rosenfeld, M.5
Davis, S.6
Brumback, L.7
Gustafsson, P.8
Ratjen, F.9
-
30
-
-
34250190592
-
An official american thoracic society/european respiratory society statement: Pulmonary function testing in preschool children
-
Beydon N, Davis SD, Lombardi E, Allen JL, Arets HGM, Aurora P, Bisgaard H, Davis GM, Ducharme FM, Eigen H, et-al. An official american thoracic society/european respiratory society statement: pulmonary function testing in preschool children. Am. J. Respir. Crit. Care Med. 2007; 175: 1304-1345.
-
(2007)
Am. J. Respir. Crit. Care Med.
, vol.175
, pp. 1304-1345
-
-
Beydon, N.1
Davis, S.D.2
Lombardi, E.3
Allen, J.L.4
Arets, H.G.M.5
Aurora, P.6
Bisgaard, H.7
Davis, G.M.8
Ducharme, F.M.9
Eigen, H.10
-
31
-
-
84860477440
-
A realistic validation study of a new nitrogen multiple-breath washout system
-
Singer F, Houltz B, Latzin P, Robinson P, Gustafsson P,. A realistic validation study of a new nitrogen multiple-breath washout system. PLoS ONE 2012; 7: e36083.
-
(2012)
PLoS ONE
, vol.7
-
-
Singer, F.1
Houltz, B.2
Latzin, P.3
Robinson, P.4
Gustafsson, P.5
-
32
-
-
0346121620
-
Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis
-
Gustafsson PM, Aurora P, Lindblad A,. Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis. Eur. Respir. J. 2003; 22: 972-979.
-
(2003)
Eur. Respir. J.
, vol.22
, pp. 972-979
-
-
Gustafsson, P.M.1
Aurora, P.2
Lindblad, A.3
-
33
-
-
84861226870
-
Lung function distinguishes preschool children with CF from healthy controls in a multi-center setting
-
Kerby GS, Rosenfeld M, Ren CL, Mayer OH, Brumback L, Castile R, Hart MA, Hiatt P, Kloster M, Johnson R, et-al. Lung function distinguishes preschool children with CF from healthy controls in a multi-center setting. Pediatr. Pulmonol. 2012; 47: 597-605.
-
(2012)
Pediatr. Pulmonol.
, vol.47
, pp. 597-605
-
-
Kerby, G.S.1
Rosenfeld, M.2
Ren, C.L.3
Mayer, O.H.4
Brumback, L.5
Castile, R.6
Hart, M.A.7
Hiatt, P.8
Kloster, M.9
Johnson, R.10
-
34
-
-
0036644653
-
Spirometry in 3- to 6-year-old children with cystic fibrosis
-
Marostica PJ, Weist AD, Eigen H, Angelicchio C, Christoph K, Savage J, Grant D, Tepper RS,. Spirometry in 3- to 6-year-old children with cystic fibrosis. Am. J. Respir. Crit. Care Med. 2002; 166: 67-71.
-
(2002)
Am. J. Respir. Crit. Care Med.
, vol.166
, pp. 67-71
-
-
Marostica, P.J.1
Weist, A.D.2
Eigen, H.3
Angelicchio, C.4
Christoph, K.5
Savage, J.6
Grant, D.7
Tepper, R.S.8
-
35
-
-
84888074505
-
Evidence of diminished FEV1 and FVC in 6-year-olds followed in the European cystic fibrosis patient registry, 2007-2009
-
VanDevanter DR, Pasta DJ,. Evidence of diminished FEV1 and FVC in 6-year-olds followed in the European cystic fibrosis patient registry, 2007-2009. J. Cyst. Fibros. 2013; 12: 786-789.
-
(2013)
J. Cyst. Fibros.
, vol.12
, pp. 786-789
-
-
Vandevanter, D.R.1
Pasta, D.J.2
-
36
-
-
12744277962
-
Multiple-breath washout as a marker of lung disease in preschool children with cystic fibrosis
-
Aurora P, Bush A, Gustafsson P, Oliver C, Wallis C, Price J, Stroobant J, Carr S, Stocks J,. 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
Oliver, C.4
Wallis, C.5
Price, J.6
Stroobant, J.7
Carr, S.8
Stocks, J.9
-
37
-
-
77951983616
-
Multiple-breath inert gas washout test and early cystic fibrosis lung disease
-
Aurora P,. Multiple-breath inert gas washout test and early cystic fibrosis lung disease. Thorax 2010; 65: 373-374.
-
(2010)
Thorax
, vol.65
, pp. 373-374
-
-
Aurora, P.1
-
38
-
-
84872175310
-
Lung function from infancy to preschool in a cohort of children with cystic fibrosis
-
Brumback LC, Davis SD, Kerby GS, Kloster M, Johnson R, Castile R, Hiatt PW, Hart M, Rosenfeld M,. Lung function from infancy to preschool in a cohort of children with cystic fibrosis. Eur. Respir. J. 2013; 41: 60-66.
-
(2013)
Eur. Respir. J.
, vol.41
, pp. 60-66
-
-
Brumback, L.C.1
Davis, S.D.2
Kerby, G.S.3
Kloster, M.4
Johnson, R.5
Castile, R.6
Hiatt, P.W.7
Hart, M.8
Rosenfeld, M.9
-
39
-
-
46349106358
-
Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis
-
Kozlowska WJ, Bush A, Wade A, Aurora P, Carr SB, Castle RA, Hoo AF, Lum S, Price J, Ranganathan S, 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.
-
(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
-
40
-
-
21744460289
-
Standardisation of spirometry
-
Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, Crapo R, Enright P, van der Grinten CP, Gustafsson P, et-al. Standardisation of spirometry. Eur. Respir. J. 2005; 26: 319-338.
-
(2005)
Eur. Respir. J.
, vol.26
, pp. 319-338
-
-
Miller, M.R.1
Hankinson, J.2
Brusasco, V.3
Burgos, F.4
Casaburi, R.5
Coates, A.6
Crapo, R.7
Enright, P.8
Van Der Grinten, C.P.9
Gustafsson, P.10
-
41
-
-
0026520359
-
Prediction of mortality in patients with cystic fibrosis
-
Kerem E, Reisman J, Corey M, Canny GJ, Levison H,. Prediction of mortality in patients with cystic fibrosis. N. Engl. J. Med. 1992; 326: 1187-1191.
-
(1992)
N. Engl. J. Med.
, vol.326
, pp. 1187-1191
-
-
Kerem, E.1
Reisman, J.2
Corey, M.3
Canny, G.J.4
Levison, H.5
-
42
-
-
2542496991
-
Serial lung function and responsiveness in cystic fibrosis during early childhood
-
Nielsen KG, Pressler T, Klug B, Koch C, Bisgaard H,. Serial lung function and responsiveness in cystic fibrosis during early childhood. Am. J. Respir. Crit. Care Med. 2004; 169: 1209-1216.
-
(2004)
Am. J. Respir. Crit. Care Med.
, vol.169
, pp. 1209-1216
-
-
Nielsen, K.G.1
Pressler, T.2
Klug, B.3
Koch, C.4
Bisgaard, H.5
-
43
-
-
0031877490
-
Airway inflammation after treatment with aerosolized deoxyribonuclease in cystic fibrosis
-
Henry RL, Gibson PG, Carty K, Cai Y, Francis JL,. Airway inflammation after treatment with aerosolized deoxyribonuclease in cystic fibrosis. Pediatr. Pulmonol. 1998; 26: 97-100.
-
(1998)
Pediatr. Pulmonol.
, vol.26
, pp. 97-100
-
-
Henry, R.L.1
Gibson, P.G.2
Carty, K.3
Cai, Y.4
Francis, J.L.5
-
44
-
-
0029188241
-
Sputum peroxidase activity correlates with the severity of lung disease in cystic fibrosis
-
Regelmann WE, Siefferman CM, Herron JM, Elliott GR, Clawson CC, Gray BH,. Sputum peroxidase activity correlates with the severity of lung disease in cystic fibrosis. Pediatr. Pulmonol. 1995; 19: 1-9.
-
(1995)
Pediatr. Pulmonol.
, vol.19
, pp. 1-9
-
-
Regelmann, W.E.1
Siefferman, C.M.2
Herron, J.M.3
Elliott, G.R.4
Clawson, C.C.5
Gray, B.H.6
-
45
-
-
0036907325
-
Induced sputum inflammatory measures correlate with lung function in children with cystic fibrosis
-
Sagel SD, Sontag MK, Wagener JS, Kapsner RK, Osberg I, Accurso FJ,. Induced sputum inflammatory measures correlate with lung function in children with cystic fibrosis. J. Pediatr. 2002; 141: 811-817.
-
(2002)
J. Pediatr.
, vol.141
, pp. 811-817
-
-
Sagel, S.D.1
Sontag, M.K.2
Wagener, J.S.3
Kapsner, R.K.4
Osberg, I.5
Accurso, F.J.6
-
46
-
-
0041353720
-
Longitudinal evaluation of bronchopulmonary disease in children with cystic fibrosis
-
Farrell PM, Li Z, Kosorok MR, Laxova A, Green CG, Collins J, Lai HC, Makholm LM, Rock MJ, Splaingard ML,. Longitudinal evaluation of bronchopulmonary disease in children with cystic fibrosis. Pediatr. Pulmonol. 2003; 36: 230-240.
-
(2003)
Pediatr. Pulmonol.
, vol.36
, pp. 230-240
-
-
Farrell, P.M.1
Li, Z.2
Kosorok, M.R.3
Laxova, A.4
Green, C.G.5
Collins, J.6
Lai, H.C.7
Makholm, L.M.8
Rock, M.J.9
Splaingard, M.L.10
-
47
-
-
0031978495
-
Pulmonary evolution of cystic fibrosis patients colonized by Pseudomonas aeruginosa and/or Burkholderia cepacia
-
Jacques I, Derelle J, Weber M, M, Vidailhet M,. Pulmonary evolution of cystic fibrosis patients colonized by Pseudomonas aeruginosa and/or Burkholderia cepacia. Eur. J. Pediatr. 1998; 157: 427-431.
-
(1998)
Eur. J. Pediatr.
, vol.157
, pp. 427-431
-
-
Jacques, I.1
Derelle, J.2
Weber, M.M.3
Vidailhet, M.4
-
48
-
-
0035002870
-
Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis
-
Nixon GM, Armstrong DS, Carzino R, Carlin JB, Olinsky A, Robertson CF, Grimwood K,. Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis. J. Pediatr. 2001; 138: 699-704.
-
(2001)
J. Pediatr.
, vol.138
, pp. 699-704
-
-
Nixon, G.M.1
Armstrong, D.S.2
Carzino, R.3
Carlin, J.B.4
Olinsky, A.5
Robertson, C.F.6
Grimwood, K.7
-
49
-
-
0029177535
-
Effects of pseudomonas aeruginosa colonization on lung function and anthropometric variables in children with cystic fibrosis
-
Pamukcu A, Bush A, Buchdahl R,. Effects of pseudomonas aeruginosa colonization on lung function and anthropometric variables in children with cystic fibrosis. Pediatr. Pulmonol. 1995; 19: 10-15.
-
(1995)
Pediatr. Pulmonol.
, vol.19
, pp. 10-15
-
-
Pamukcu, A.1
Bush, A.2
Buchdahl, R.3
-
50
-
-
33845775361
-
Progression of pulmonary hyperinflation and trapped gas associated with genetic and environmental factors in children with cystic fibrosis
-
Kraemer R, Baldwin DN, Ammann RA, Frey U, Gallati S,. Progression of pulmonary hyperinflation and trapped gas associated with genetic and environmental factors in children with cystic fibrosis. Respir. Res. 2006; 7: 138.
-
(2006)
Respir. Res.
, vol.7
, pp. 138
-
-
Kraemer, R.1
Baldwin, D.N.2
Ammann, R.A.3
Frey, U.4
Gallati, S.5
-
51
-
-
33845542156
-
Effect of allergic bronchopulmonary aspergillosis on lung function in children with cystic fibrosis
-
Kraemer R, Delosea N, Ballinari P, Gallati S, Crameri R,. Effect of allergic bronchopulmonary aspergillosis on lung function in children with cystic fibrosis. Am. J. Respir. Crit. Care Med. 2006; 174: 1211-1220.
-
(2006)
Am. J. Respir. Crit. Care Med.
, vol.174
, pp. 1211-1220
-
-
Kraemer, R.1
Delosea, N.2
Ballinari, P.3
Gallati, S.4
Crameri, R.5
-
52
-
-
84881381613
-
Practicability of nitrogen multiple-breath washout measurements in a pediatric cystic fibrosis outpatient setting
-
Singer F, Kieninger E, Abbas C, Yammine S, Fuchs O, Proietti E, Regamey N, Casaulta C, Frey U, Latzin P,. Practicability of nitrogen multiple-breath washout measurements in a pediatric cystic fibrosis outpatient setting. Pediatr. Pulmonol. 2013; 48: 739-746.
-
(2013)
Pediatr. Pulmonol.
, vol.48
, pp. 739-746
-
-
Singer, F.1
Kieninger, E.2
Abbas, C.3
Yammine, S.4
Fuchs, O.5
Proietti, E.6
Regamey, N.7
Casaulta, C.8
Frey, U.9
Latzin, P.10
-
53
-
-
78650016662
-
Sensitivity of Lung Clearance Index and chest computed tomography in early CF lung disease
-
Ellemunter H, Fuchs SI, Unsinn KM, Freund MC, Waltner-Romen M, Steinkamp G, Gappa M,. Sensitivity of Lung Clearance Index and chest computed tomography in early CF lung disease. Respir. Med. 2010; 104: 1834-1842.
-
(2010)
Respir. Med.
, vol.104
, pp. 1834-1842
-
-
Ellemunter, H.1
Fuchs, S.I.2
Unsinn, K.M.3
Freund, M.C.4
Waltner-Romen, M.5
Steinkamp, G.6
Gappa, M.7
-
54
-
-
0033531143
-
Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic Fibrosis Inhaled Tobramycin Study Group
-
Ramsey BW, Pepe MS, Quan JM, Otto KL, Montgomery AB, Williams-Warren J, Vasiljev KM, Borowitz D, Bowman CM, Marshall BC, et-al. Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic Fibrosis Inhaled Tobramycin Study Group. N. Engl. J. Med. 1999; 340: 23-30.
-
(1999)
N. Engl. J. Med.
, vol.340
, pp. 23-30
-
-
Ramsey, B.W.1
Pepe, M.S.2
Quan, J.M.3
Otto, K.L.4
Montgomery, A.B.5
Williams-Warren, J.6
Vasiljev, K.M.7
Borowitz, D.8
Bowman, C.M.9
Marshall, B.C.10
-
55
-
-
0019940570
-
Serial changes in pulmonary functions in children hospitalized with cystic fibrosis
-
Redding GJ, Restuccia R, Cotton EK, Brooks JG,. Serial changes in pulmonary functions in children hospitalized with cystic fibrosis. Am. Rev. Respir. Dis. 1982; 126: 31-36.
-
(1982)
Am. Rev. Respir. Dis.
, vol.126
, pp. 31-36
-
-
Redding, G.J.1
Restuccia, R.2
Cotton, E.K.3
Brooks, J.G.4
-
56
-
-
0028129568
-
Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group
-
Fuchs HJ, Borowitz DS, Christiansen DH, Morris EM, Nash ML, Ramsey BW, Rosenstein BJ, Smith AL, Wohl ME,. 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.
-
(1994)
N. Engl. J. Med.
, vol.331
, 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
-
57
-
-
30944466084
-
A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis
-
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.
-
(2006)
N. Engl. J. Med.
, vol.354
, 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.9
-
58
-
-
84877593162
-
Changes in physiological, functional and structural markers of cystic fibrosis lung disease with treatment of a pulmonary exacerbation
-
Horsley AR, Davies JC, Gray RD, Macleod KA, Donovan J, Aziz ZA, Bell NJ, Rainer M, Mt-Isa S, Voase N, et-al. Changes in physiological, functional and structural markers of cystic fibrosis lung disease with treatment of a pulmonary exacerbation. Thorax 2013; 68: 532-539.
-
(2013)
Thorax
, vol.68
, pp. 532-539
-
-
Horsley, A.R.1
Davies, J.C.2
Gray, R.D.3
MacLeod, K.A.4
Donovan, J.5
Aziz, Z.A.6
Bell, N.J.7
Rainer, M.8
Mt-Isa, S.9
Voase, N.10
-
59
-
-
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
-
60
-
-
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, et-al. 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
-
61
-
-
84885071273
-
Assessment of clinical response to ivacaftor with lung clearance index in cystic fi brosis patients with a G551D-CFTR mutation and preserved spirometry: A randomised controlled trial in patients with a G551D-CFTR mutation and preserved spirometry: A randomised controlled trial
-
Davies J, Sheridan H, Bell NJ, Cunningham S, Davis S, Elborn J, Milla CE, Starner TD, Weiner DJ, Lee P, et-al. Assessment of clinical response to ivacaftor with lung clearance index in cystic fi brosis patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trial in patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trial. Lancet Respir. Med. 2013; 1: 630-638.
-
(2013)
Lancet Respir. Med.
, vol.1
, pp. 630-638
-
-
Davies, J.1
Sheridan, H.2
Bell, N.J.3
Cunningham, S.4
Davis, S.5
Elborn, J.6
Milla, C.E.7
Starner, T.D.8
Weiner, D.J.9
Lee, P.10
-
62
-
-
68049093796
-
Using index of ventilation to assess response to treatment for acute pulmonary exacerbation in children with cystic fibrosis
-
Robinson PD, Cooper P, Van Asperen P, Fitzgerald D, Selvadurai H,. Using index of ventilation to assess response to treatment for acute pulmonary exacerbation in children with cystic fibrosis. Pediatr. Pulmonol. 2009; 44: 733-742.
-
(2009)
Pediatr. Pulmonol.
, vol.44
, pp. 733-742
-
-
Robinson, P.D.1
Cooper, P.2
Van Asperen, P.3
Fitzgerald, D.4
Selvadurai, H.5
-
63
-
-
84892549397
-
Reasons for heterogeneous change in LCI in children with cystic fibrosis after antibiotic treatment
-
Yammine S, Bigler A, Casaulta C, Singer F, Latzin P,. Reasons for heterogeneous change in LCI in children with cystic fibrosis after antibiotic treatment. Thorax 2014; 69: 183.
-
(2014)
Thorax
, vol.69
, pp. 183
-
-
Yammine, S.1
Bigler, A.2
Casaulta, C.3
Singer, F.4
Latzin, P.5
-
64
-
-
84904576258
-
-
European Respiratory Society Annual Congress, Barcelona Spain.
-
Welsh L, Tomai M, Tran H, Ranganathan S,. Lung Clearance Index during Pulmonary Exacerbation in School-age Children with Cystic Fibrosis. European Respiratory Society Annual Congress, Barcelona Spain, 2013.
-
(2013)
Lung Clearance Index during Pulmonary Exacerbation in School-age Children with Cystic Fibrosis
-
-
Welsh, L.1
Tomai, M.2
Tran, H.3
Ranganathan, S.4
-
65
-
-
66149130974
-
Longitudinal assessment of lung function from infancy to childhood in patients with cystic fibrosis
-
Harrison AN, Regelmann WE, Zirbes JM, Milla CE,. Longitudinal assessment of lung function from infancy to childhood in patients with cystic fibrosis. Pediatr. Pulmonol. 2009; 44: 330-339.
-
(2009)
Pediatr. Pulmonol.
, vol.44
, pp. 330-339
-
-
Harrison, A.N.1
Regelmann, W.E.2
Zirbes, J.M.3
Milla, C.E.4
-
66
-
-
13544250572
-
Ventilation inhomogeneities in relation to standard lung function in patients with cystic fibrosis
-
Kraemer R, Blum A, Schibler A, Ammann RA, Gallati S,. Ventilation inhomogeneities in relation to standard lung function in patients with cystic fibrosis. Am. J. Respir. Crit. Care Med. 2005; 171: 371-378.
-
(2005)
Am. J. Respir. Crit. Care Med.
, vol.171
, pp. 371-378
-
-
Kraemer, R.1
Blum, A.2
Schibler, A.3
Ammann, R.A.4
Gallati, S.5
-
67
-
-
0030959076
-
A prognostic model for the prediction of survival in cystic fibrosis
-
Hayllar KM, Williams SG, Wise AE, et-al. A prognostic model for the prediction of survival in cystic fibrosis. Thorax 1997; 52: 313-317.
-
(1997)
Thorax
, vol.52
, pp. 313-317
-
-
Hayllar, K.M.1
Williams, S.G.2
Wise, A.E.3
-
68
-
-
81455154503
-
Long-term course of lung clearance index between infancy and school-age in cystic fibrosis subjects
-
Kieninger E, Singer F, Fuchs O, Abbas C, Frey U, Regamey N, Casaulta C, Latzin P,. Long-term course of lung clearance index between infancy and school-age in cystic fibrosis subjects. J. Cyst. Fibros. 2011; 10: 487-490.
-
(2011)
J. Cyst. Fibros.
, vol.10
, pp. 487-490
-
-
Kieninger, E.1
Singer, F.2
Fuchs, O.3
Abbas, C.4
Frey, U.5
Regamey, N.6
Casaulta, C.7
Latzin, P.8
-
69
-
-
79952504576
-
Lung clearance index at 4 years predicts subsequent lung function in children with cystic fibrosis
-
Aurora P, Stanojevic S, Wade A, Oliver C, Kozlowska W, Lum S, Bush A, Price J, Carr SB, Shankar A, et-al. Lung clearance index at 4 years predicts subsequent lung function in children with cystic fibrosis. Am. J. Respir. Crit. Care Med. 2011; 183: 752-758.
-
(2011)
Am. J. Respir. Crit. Care Med.
, vol.183
, pp. 752-758
-
-
Aurora, P.1
Stanojevic, S.2
Wade, A.3
Oliver, C.4
Kozlowska, W.5
Lum, S.6
Bush, A.7
Price, J.8
Carr, S.B.9
Shankar, A.10
-
70
-
-
84890309789
-
Lung clearance index predicts pulmonary exacerbations in young patients with cystic fibrosis
-
Vermeulen F, Proesmans M, Boon M, Havermans T, De Boeck K,. Lung clearance index predicts pulmonary exacerbations in young patients with cystic fibrosis. Thorax 2014; 69: 39-45.
-
(2014)
Thorax
, vol.69
, pp. 39-45
-
-
Vermeulen, F.1
Proesmans, M.2
Boon, M.3
Havermans, T.4
De Boeck, K.5
-
71
-
-
0028863684
-
Lung function from infancy to school age in cystic fibrosis
-
Beardsmore CS,. Lung function from infancy to school age in cystic fibrosis. Arch. Dis. Child. 1995; 73: 519-523.
-
(1995)
Arch. Dis. Child.
, vol.73
, pp. 519-523
-
-
Beardsmore, C.S.1
-
72
-
-
0023777791
-
Lung function in infants with cystic fibrosis
-
Beardsmore CS, Bar-Yishay E, Maayan C, Yahav Y, Katznelson D, Godfrey S,. Lung function in infants with cystic fibrosis. Thorax 1988; 43: 545-551.
-
(1988)
Thorax
, vol.43
, pp. 545-551
-
-
Beardsmore, C.S.1
Bar-Yishay, E.2
Maayan, C.3
Yahav, Y.4
Katznelson, D.5
Godfrey, S.6
-
73
-
-
0017879314
-
Serial lung function studies in cystic fibrosis in the first 5 years of life
-
Godfrey S, Mearns M, Howlett G,. Serial lung function studies in cystic fibrosis in the first 5 years of life. Arch. Dis. Child. 1978; 53: 83-85.
-
(1978)
Arch. Dis. Child.
, vol.53
, pp. 83-85
-
-
Godfrey, S.1
Mearns, M.2
Howlett, G.3
-
74
-
-
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
-
75
-
-
0023757636
-
Infants with cystic fibrosis: Pulmonary function at diagnosis
-
Tepper RS, Hiatt P, Eigen H, Scott P, Grosfeld J, Cohen M,. Infants with cystic fibrosis: pulmonary function at diagnosis. Pediatr. Pulmonol. 1988; 5: 15-18.
-
(1988)
Pediatr. Pulmonol.
, vol.5
, pp. 15-18
-
-
Tepper, R.S.1
Hiatt, P.2
Eigen, H.3
Scott, P.4
Grosfeld, J.5
Cohen, M.6
-
76
-
-
0027652118
-
Longitudinal evaluation of pulmonary function in infants and very young children with cystic fibrosis
-
Tepper RS, Montgomery GL, Ackerman V, Eigen H,. Longitudinal evaluation of pulmonary function in infants and very young children with cystic fibrosis. Pediatr. Pulmonol. 1993; 16: 96-100.
-
(1993)
Pediatr. Pulmonol.
, vol.16
, pp. 96-100
-
-
Tepper, R.S.1
Montgomery, G.L.2
Ackerman, V.3
Eigen, H.4
-
77
-
-
23644454805
-
Gas mixing efficiency from birth to adulthood measured by multiple-breath washout
-
Aurora P, Kozlowska W, Stocks J,. Gas mixing efficiency from birth to adulthood measured by multiple-breath washout. Respir. Physiol. Neurobiol. 2005; 148: 125-139.
-
(2005)
Respir. Physiol. Neurobiol.
, vol.148
, pp. 125-139
-
-
Aurora, P.1
Kozlowska, W.2
Stocks, J.3
-
78
-
-
9644259076
-
Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis
-
Aurora P, Gustafsson P, Bush A, Lindblad A, Oliver C, Wallis CE, Stocks J,. Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis. Thorax 2004; 59: 1068-1073.
-
(2004)
Thorax
, vol.59
, pp. 1068-1073
-
-
Aurora, P.1
Gustafsson, P.2
Bush, A.3
Lindblad, A.4
Oliver, C.5
Wallis, C.E.6
Stocks, J.7
-
79
-
-
84878792913
-
Age and height dependence of lung clearance index and functional residual capacity
-
Lum S, Stocks J, Stanojevic S, Wade A, Robinson P, Gustafsson P, Brown M, Aurora P, Subbarao P, Hoo AF, et-al. Age and height dependence of lung clearance index and functional residual capacity. Eur. Respir. J. 2013; 41: 1371-1377.
-
(2013)
Eur. Respir. J.
, vol.41
, pp. 1371-1377
-
-
Lum, S.1
Stocks, J.2
Stanojevic, S.3
Wade, A.4
Robinson, P.5
Gustafsson, P.6
Brown, M.7
Aurora, P.8
Subbarao, P.9
Hoo, A.F.10
-
80
-
-
84874103198
-
Multiple breath nitrogen washout: A feasible alternative to mass spectrometry
-
Jensen R, Stanojevic S, Gibney K, Salazar JG, Gustafsson P, Subbarao P, Ratjen F,. Multiple breath nitrogen washout: a feasible alternative to mass spectrometry. PLoS ONE 2013; 8: e56868.
-
(2013)
PLoS ONE
, vol.8
-
-
Jensen, R.1
Stanojevic, S.2
Gibney, K.3
Salazar, J.G.4
Gustafsson, P.5
Subbarao, P.6
Ratjen, F.7
-
81
-
-
84875266201
-
Consensus statement for inert gas washout measurement using multiple- and single-breath tests
-
Robinson PD, Latzin P, Verbanck S, Hall GL, Horsley A, Gappa M, Thamrin C, Arets HG, Aurora P, Fuchs SI, et-al. Consensus statement for inert gas washout measurement using multiple- and single-breath tests. Eur. Respir. J. 2013; 41: 507-522.
-
(2013)
Eur. Respir. J.
, vol.41
, pp. 507-522
-
-
Robinson, P.D.1
Latzin, P.2
Verbanck, S.3
Hall, G.L.4
Horsley, A.5
Gappa, M.6
Thamrin, C.7
Arets, H.G.8
Aurora, P.9
Fuchs, S.I.10
-
82
-
-
0036107651
-
Exploring the relationship between forced maximal flow at functional residual capacity and parameters of forced expiration from raised lung volume in healthy infants
-
Ranganathan SC, Hoo AF, Lum SY, Goetz I, Castle RA, Stocks J,. Exploring the relationship between forced maximal flow at functional residual capacity and parameters of forced expiration from raised lung volume in healthy infants. Pediatr. Pulmonol. 2002; 33: 419-428.
-
(2002)
Pediatr. Pulmonol.
, vol.33
, pp. 419-428
-
-
Ranganathan, S.C.1
Hoo, A.F.2
Lum, S.Y.3
Goetz, I.4
Castle, R.A.5
Stocks, J.6
-
83
-
-
84867087485
-
Cystic fibrosis: The role of the small airways
-
Ratjen F,. Cystic fibrosis: the role of the small airways. J. Aerosol Med. Pulm. Drug Deliv. 2012; 25: 261-264.
-
(2012)
J. Aerosol Med. Pulm. Drug Deliv.
, vol.25
, pp. 261-264
-
-
Ratjen, F.1
-
84
-
-
0034764166
-
Early pulmonary infection, inflammation, and clinical outcomes in infants with cystic fibrosis
-
Rosenfeld M, Gibson RL, McNamara S, Emerson J, Burns JL, Castile R, Hiatt P, McCoy K, Wilson CB, Inglis A, et-al. Early pulmonary infection, inflammation, and clinical outcomes in infants with cystic fibrosis. Pediatr. Pulmonol. 2001; 32: 356-366.
-
(2001)
Pediatr. Pulmonol.
, vol.32
, pp. 356-366
-
-
Rosenfeld, M.1
Gibson, R.L.2
McNamara, S.3
Emerson, J.4
Burns, J.L.5
Castile, R.6
Hiatt, P.7
McCoy, K.8
Wilson, C.B.9
Inglis, A.10
-
85
-
-
80052014087
-
Inflammatory responses to individual microorganisms in the lungs of children with cystic fibrosis
-
Gangell C, Gard S, Douglas T, Park J, de Klerk N, Keil T, Brennan S, Ranganathan S, Robins-Browne R, Sly PD,. 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
-
86
-
-
0025270107
-
Haemophilus infection in cystic fibrosis
-
Rayner RJ, Hiller EJ, Ispahani P, Baker M,. Haemophilus infection in cystic fibrosis. Arch. Dis. Child. 1990; 65: 255-258.
-
(1990)
Arch. Dis. Child.
, vol.65
, pp. 255-258
-
-
Rayner, R.J.1
Hiller, E.J.2
Ispahani, P.3
Baker, M.4
-
87
-
-
74949096500
-
The effect of chronic infection with Aspergillus fumigatus on lung function and hospitalization in patients with cystic fibrosis
-
Amin R, Dupuis A, Aaron SD, Ratjen F,. The effect of chronic infection with Aspergillus fumigatus on lung function and hospitalization in patients with cystic fibrosis. Chest 2010; 137: 171-176.
-
(2010)
Chest
, vol.137
, pp. 171-176
-
-
Amin, R.1
Dupuis, A.2
Aaron, S.D.3
Ratjen, F.4
-
88
-
-
0031471090
-
Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis
-
Corey M, Edwards L, Levison H, Knowles M,. Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis. J. Pediatr. 1997; 131: 809-814.
-
(1997)
J. Pediatr.
, vol.131
, pp. 809-814
-
-
Corey, M.1
Edwards, L.2
Levison, H.3
Knowles, M.4
-
89
-
-
78649838472
-
Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints
-
Davis SD, Rosenfeld M, Kerby GS, Brumback L, Kloster MH, Acton JD, Colin AA, Conrad CK, Hart MA, Hiatt PW, et-al. Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints. Am. J. Respir. Crit. Care Med. 2010; 182: 1387-1397.
-
(2010)
Am. J. Respir. Crit. Care Med.
, vol.182
, pp. 1387-1397
-
-
Davis, S.D.1
Rosenfeld, M.2
Kerby, G.S.3
Brumback, L.4
Kloster, M.H.5
Acton, J.D.6
Colin, A.A.7
Conrad, C.K.8
Hart, M.A.9
Hiatt, P.W.10
-
90
-
-
0034014273
-
Forced expiratory flows and volumes in infants. Normative data and lung growth
-
Jones M, Castile R, Davis S, Kisling J, Filbrun D, Flucke R, Goldstein A, Emsley C, Ambrosius W, Tepper RS,. Forced expiratory flows and volumes in infants. Normative data and lung growth. Am. J. Respir. Crit. Care Med. 2000; 161: 353-359.
-
(2000)
Am. J. Respir. Crit. Care Med.
, vol.161
, pp. 353-359
-
-
Jones, M.1
Castile, R.2
Davis, S.3
Kisling, J.4
Filbrun, D.5
Flucke, R.6
Goldstein, A.7
Emsley, C.8
Ambrosius, W.9
Tepper, R.S.10
-
91
-
-
77956498322
-
Clinically useful spirometry in preschool-aged children: Evaluation of the 2007 American Thoracic Society Guidelines
-
Gaffin JM, Shotola NL, Martin TR, Phipatanakul W,. Clinically useful spirometry in preschool-aged children: evaluation of the 2007 American Thoracic Society Guidelines. J. Asthma 2010; 47: 762-767.
-
(2010)
J. Asthma
, vol.47
, pp. 762-767
-
-
Gaffin, J.M.1
Shotola, N.L.2
Martin, T.R.3
Phipatanakul, W.4
-
92
-
-
84863437624
-
Multi-ethnic reference values for spirometry for the 3-95-yr age range: The global lung function 2012 equations
-
Quanjer PH, Stanojevic S, Cole TJ, Baur X, Hall GL, Culver BH, Enright PL, Hankinson JL, Ip MS, Zheng J, et-al. Multi-ethnic reference values for spirometry for the 3-95-yr age range: the global lung function 2012 equations. Eur. Respir. J. 2012; 40: 1324-1343.
-
(2012)
Eur. Respir. J.
, vol.40
, pp. 1324-1343
-
-
Quanjer, P.H.1
Stanojevic, S.2
Cole, T.J.3
Baur, X.4
Hall, G.L.5
Culver, B.H.6
Enright, P.L.7
Hankinson, J.L.8
Ip, M.S.9
Zheng, J.10
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