-
1
-
-
67650712233
-
Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening
-
Sly P.D., Brennan S., Gangell C., de Klerk N., Murray C., Mott L., et al. 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
-
2
-
-
70349831005
-
Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening
-
Stick S.M., Brennan S., Murray C., Douglas T., von Ungern-Sternberg B.S., Garratt L.W., et al. Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening. J Pediatr 2009, 155:623-628.
-
(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
-
3
-
-
80051850244
-
Air trapping on chest CT is associated with worse ventilation distribution in infants with cystic fibrosis diagnosed following newborn screening
-
Hall G.L., Logie K.M., Parsons F., Schulzke S.M., Nolan G., Murray C., 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(8):e23932.
-
(2011)
PLoS One
, vol.6
, Issue.8
-
-
Hall, G.L.1
Logie, K.M.2
Parsons, F.3
Schulzke, S.M.4
Nolan, G.5
Murray, C.6
-
4
-
-
84866070431
-
Lung function is abnormal in 3-month-old infants with cystic fibrosis diagnosed by newborn screening
-
Hoo A.F., Thia L.P., Nguyen T.T., Bush A., Chudleigh J., Lum S., 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
-
5
-
-
84862776813
-
Progression of early structural lung disease in young children with cystic fibrosis assessed using CT
-
Mott L.S., Park J., Murray C.P., Gangell C.L., de Klerk N.H., Robinson P.J., et al. Progression of early structural lung disease in young children with cystic fibrosis assessed using CT. Thorax 2012, 67(6):509-516.
-
(2012)
Thorax
, vol.67
, Issue.6
, 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
-
6
-
-
84863437624
-
ERS Global Lung Function Initiative. Multi-ethnic reference values for spirometry for the 3-95-yr age range: the global lung function 2012 equations
-
Quanjer P.H., Stanojevic S., Cole T.J., Baur X., Hall G.L., Culver B.H., et al. ERS Global Lung Function Initiative. Multi-ethnic reference values for spirometry for the 3-95-yr age range: the global lung function 2012 equations. Eur Respir J 2012, 40(6):1324-1343.
-
(2012)
Eur Respir J
, vol.40
, Issue.6
, 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
-
7
-
-
67949095989
-
Characterizing aggressiveness and predicting future progression of CF lung disease
-
Konstan M.W., Wagener J.S., VanDevanter D.R. Characterizing aggressiveness and predicting future progression of CF lung disease. J Cyst Fibros 2009, 8S:S15-S19.
-
(2009)
J Cyst Fibros
, vol.8 S
-
-
Konstan, M.W.1
Wagener, J.S.2
VanDevanter, D.R.3
-
8
-
-
34147215995
-
Exacerbations in cystic fibrosis. 1: epidemiology and pathogenesis
-
[Review]
-
Goss C.H., Burns J.L. Exacerbations in cystic fibrosis. 1: epidemiology and pathogenesis. Thorax 2007, 62(4):360-367. [Review].
-
(2007)
Thorax
, vol.62
, Issue.4
, pp. 360-367
-
-
Goss, C.H.1
Burns, J.L.2
-
9
-
-
0026520359
-
Prediction of mortality in patients with cystic fibrosis
-
Kerem E., Reisman J., Corey M., Canny G.J., 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
-
11
-
-
84886379324
-
Small airway involvement in cystic fibrosis lung disease: routine spirometry as an early and sensitive marker
-
[Epub ahead of print]
-
Bakker E.M., Borsboom G.J., van der Wiel-Kooij E.C., Caudri D., Rosenfeld M., Tiddens H.A. Small airway involvement in cystic fibrosis lung disease: routine spirometry as an early and sensitive marker. Pediatr Pulmonol Feb 8 2013, [Epub ahead of print]. 10.1002/ppul.22777.
-
(2013)
Pediatr Pulmonol
-
-
Bakker, E.M.1
Borsboom, G.J.2
van der Wiel-Kooij, E.C.3
Caudri, D.4
Rosenfeld, M.5
Tiddens, H.A.6
-
12
-
-
79956360940
-
Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF
-
Owens C.M., Aurora P., Stanojevic S., Bush A., Wade A., Oliver C., et al. Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF. Thorax 2011, 66(6):481-488.
-
(2011)
Thorax
, vol.66
, Issue.6
, pp. 481-488
-
-
Owens, C.M.1
Aurora, P.2
Stanojevic, S.3
Bush, A.4
Wade, A.5
Oliver, C.6
-
13
-
-
78649662363
-
Pulmonary outcome prediction (POP) tools for cystic fibrosis patients
-
VanDevanter D.R., Wagener J.S., Pasta D.J., Elkin E., Jacobs J.R., Morgan W.J., et al. Pulmonary outcome prediction (POP) tools for cystic fibrosis patients. Pediatr Pulmonol 2010, 45(12):1156-1166.
-
(2010)
Pediatr Pulmonol
, vol.45
, Issue.12
, pp. 1156-1166
-
-
VanDevanter, D.R.1
Wagener, J.S.2
Pasta, D.J.3
Elkin, E.4
Jacobs, J.R.5
Morgan, W.J.6
-
14
-
-
46349106358
-
Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis
-
Kozlowska W.J., Bush A., Wade A., Aurora P., Carr S.B., Castle R.A., et al. Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis. Am J Respir Crit Care Med 2008, 178(1):42-49.
-
(2008)
Am J Respir Crit Care Med
, vol.178
, Issue.1
, pp. 42-49
-
-
Kozlowska, W.J.1
Bush, A.2
Wade, A.3
Aurora, P.4
Carr, S.B.5
Castle, R.A.6
-
15
-
-
79952504576
-
Lung clearance index at 4years predicts subsequent lung function in children with cystic fibrosis
-
Aurora P., Stanojevic S., Wade A., Oliver C., Kozlowska W., Lum S., et al. Lung clearance index at 4years predicts subsequent lung function in children with cystic fibrosis. Am J Respir Crit Care Med 2011, 183(6):752-758.
-
(2011)
Am J Respir Crit Care Med
, vol.183
, Issue.6
, pp. 752-758
-
-
Aurora, P.1
Stanojevic, S.2
Wade, A.3
Oliver, C.4
Kozlowska, W.5
Lum, S.6
|