Ventilation inhomogeneity in children with primary ciliary dyskinesia
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P. Gustafsson | K. Nielsen | F. Buchvald | Per M Gustafsson | Kent Green | Frederik F Buchvald | June Kehlet Marthin | Birgitte Hanel | Kim Gjerum Nielsen | B. Hanel | Kent Green | June K. Marthin
[1] M. Jorissen,et al. Ciliary function analysis for the diagnosis of primary ciliary dyskinesia: advantages of ciliogenesis in culture. , 2000, Acta oto-laryngologica.
[2] M. Lebowitz,et al. Maximal mid-expiratory flow (FEF25-75%): normal limits and assessment of sensitivity. , 1978, The American review of respiratory disease.
[3] P. Gustafsson. Peripheral airway involvement in CF and asthma compared by inert gas washout , 2007, Pediatric pulmonology.
[4] C. Hogg. Primary ciliary dyskinesia: when to suspect the diagnosis and how to confirm it. , 2009, Paediatric respiratory reviews.
[5] S. Gallati,et al. Ventilation inhomogeneities in relation to standard lung function in patients with cystic fibrosis. , 2005, American journal of respiratory and critical care medicine.
[6] S. Cunningham,et al. Effects of cystic fibrosis lung disease on gas mixing indices derived from alveolar slope analysis , 2008, Respiratory Physiology & Neurobiology.
[7] M. Hazucha,et al. Primary ciliary dyskinesia: diagnostic and phenotypic features. , 2004, American journal of respiratory and critical care medicine.
[8] M. Leigh,et al. Early lung disease in young children with primary ciliary dyskinesia , 2008, Pediatric pulmonology.
[9] Heterogeneous lung emptying during forced expiration. , 1987, Journal of applied physiology.
[10] P. Gustafsson,et al. Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis , 2003, European Respiratory Journal.
[11] P. Molina,et al. High-resolution computed tomography in young patients with cystic fibrosis: distribution of abnormalities and correlation with pulmonary function tests. , 2004, The Journal of pediatrics.
[12] M. Noppen,et al. Conductive and acinar lung-zone contributions to ventilation inhomogeneity in COPD. , 1998, American journal of respiratory and critical care medicine.
[13] K. Nielsen,et al. Choice of nasal nitric oxide technique as first-line test for primary ciliary dyskinesia , 2010, European Respiratory Journal.
[14] Buist As. Standardization of spirometry. , 1987 .
[15] A. Boner,et al. Health-related quality of life and unmet needs in patients with primary ciliary dyskinesia , 2009, European Respiratory Journal.
[16] S. Stanojevic,et al. Reference ranges for spirometry across all ages: a new approach. , 2008, American journal of respiratory and critical care medicine.
[17] H Omran,et al. Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in children , 2009, European Respiratory Journal.
[18] R. Wilson,et al. Ciliary disorientation: a possible variant of primary ciliary dyskinesia. , 1993, Thorax.
[19] Scott H. Donaldson,et al. Cystic fibrosis lung disease starts in the small airways: Can we treat it more effectively? , 2010, Pediatric pulmonology.
[20] H. Tiddens,et al. Structural and functional lung disease in primary ciliary dyskinesia. , 2008, Chest.
[21] A. Bush,et al. Primary ciliary dyskinesia: current state of the art , 2007, Archives of Disease in Childhood.
[22] D. Hughes. Primary ciliary dyskinesia. , 2008, Paediatrics & child health.
[23] H. Tiddens,et al. Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis , 2007, Thorax.
[24] M. Goldman,et al. Inert Gas Washout: Theoretical Background and Clinical Utility in Respiratory Disease , 2009, Respiration.
[25] 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.
[26] J. E. Hansen,et al. Discriminating measures and normal values for expiratory obstruction. , 2006, Chest.
[27] J. Mortensen,et al. Pulmonary radioaerosol mucociliary clearance in diagnosis of primary ciliary dyskinesia. , 2007, Chest.
[28] L. Skovgaard,et al. Lung function in patients with primary ciliary dyskinesia: a cross-sectional and 3-decade longitudinal study. , 2010, American journal of respiratory and critical care medicine.
[29] A. Bush,et al. Primary ciliary dyskinesia syndrome associated with abnormal ciliary orientation in infants. , 2001, The European respiratory journal.
[30] Janet Stocks,et al. Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests , 2007, Thorax.
[31] J. Stocks,et al. Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis , 2004, Thorax.
[32] Janet Stocks,et al. Multiple-breath washout as a marker of lung disease in preschool children with cystic fibrosis. , 2005, American journal of respiratory and critical care medicine.
[33] A. Bush,et al. Diagnosing primary ciliary dyskinesia , 2007, Thorax.
[34] John L. Hankinson,et al. Standardization of Spirometry, 1994 Update. American Thoracic Society. , 1995, American journal of respiratory and critical care medicine.