Airway function in infants newly diagnosed with cystic fibrosis

The lung function of infants with cystic fibrosis is often reduced shortly after diagnosis. We measured the airway function of newly diagnosed infants to test whether this reduction is independent of clinically recognised lower respiratory illness. We compared the airway function of 33 infants with...

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Veröffentlicht in:	The Lancet (British edition) 2001-12, Vol.358 (9297), p.1964-1965
Hauptverfasser:	Ranganathan, SC, Dezateux, C, Bush, A, Carr, SB, Castle, RA, Madge, S, Price, J, Stroobant, J, Wade, A, Wallis, C, Stocks, J
Format:	Artikel
Sprache:	eng
Schlagworte:	Adjustment Age Babies Body weight Case-Control Studies Children Collaboration Cystic fibrosis Cystic Fibrosis - physiopathology Davies, Sarah Female Humans Infant Infants Infections Inflammation Lung - physiology Lungs Male Medical research Regression analysis Respiratory diseases Respiratory function Respiratory Function Tests Respiratory Mechanics - physiology Respiratory tract Rosenthal, Gary Smoking
Online-Zugang:	Volltext
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