Long-term course of lung clearance index between infancy and school-age in cystic fibrosis subjects.

[1]  P. Sly,et al.  Infection, inflammation, and lung function decline in infants with cystic fibrosis. , 2011, American journal of respiratory and critical care medicine.

[2]  P. Gustafsson,et al.  The effect of dornase alfa on ventilation inhomogeneity in patients with cystic fibrosis , 2011, European Respiratory Journal.

[3]  S. Stanojevic,et al.  Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF , 2011, Thorax.

[4]  S. Stanojevic,et al.  Lung clearance index at 4 years predicts subsequent lung function in children with cystic fibrosis. , 2011, American journal of respiratory and critical care medicine.

[5]  P. Sly,et al.  Evolution of pulmonary inflammation and nutritional status in infants and young children with cystic fibrosis , 2011, Thorax.

[6]  M. Gappa,et al.  Sensitivity of Lung Clearance Index and chest computed tomography in early CF lung disease. , 2010, Respiratory medicine.

[7]  T. Riedel,et al.  Normative data for lung function and exhaled nitric oxide in unsedated healthy infants , 2010, European Respiratory Journal.

[8]  P. Aurora Multiple-breath inert gas washout test and early cystic fibrosis lung disease , 2010, Thorax.

[9]  F. Ratjen,et al.  Hypertonic saline improves the LCI in paediatric patients with CF with normal lung function , 2010, Thorax.

[10]  P. Sly,et al.  Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening. , 2009, American journal of respiratory and critical care medicine.

[11]  P. Sly,et al.  Lung function in infants with cystic fibrosis diagnosed by newborn screening. , 2008, American journal of respiratory and critical care medicine.

[12]  S. Stanojevic,et al.  Reference ranges for spirometry across all ages: a new approach. , 2008, American journal of respiratory and critical care medicine.

[13]  D. Baldwin,et al.  Optimized temperature and deadspace correction improve analysis of multiple breath washout measurements by ultrasonic flowmeter in infants , 2007, Pediatric pulmonology.

[14]  R. Kraemer,et al.  Ventilation inhomogeneities assessed by the multibreath washout (MBW) technique , 2007, Thorax.

[15]  H. Tiddens,et al.  Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis , 2007, Thorax.

[16]  A. Wade,et al.  Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests , 2007, Thorax.

[17]  J. Walt Oxygen - elixir of life or Trojan horse? Part 2: oxygen and neonatal anesthesia. , 2006 .

[18]  Johan Van Der Walt Fanzca Ffarcsi Oxygen – elixir of life or Trojan horse? Part 2: oxygen and neonatal anesthesia , 2006 .

[19]  J. Stocks,et al.  Specifications for equipment used for infant pulmonary function testing. ERS/ATS Task Force on Standards for Infant Respiratory Function Testing. European Respiratory Society/ American Thoracic Society. , 2000, The European respiratory journal.

[20]  A. B. Crawford,et al.  Convection- and diffusion-dependent ventilation maldistribution in normal subjects. , 1985, Journal of applied physiology.

[21]  P. Macklem,et al.  Airway closure: demonstration by breathing 100 percent O2 at low lung volumes and by N2 washout. , 1968, Journal of applied physiology.

[22]  J. Stocks,et al.  EARLY DETECTION OF LUNG DISEASE IN INFANTS WITH CYSTIC FIBROSIS DIAGNOSED BY NEWBORN SCREENING (NBS) , 2010 .