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• W1907761738 abstract "The median life expectancy for cystic fibrosis is now over 30 years, and it is projected that in newborn infants it will become more than 40 years. The identification of the cystic fibrosis gene and its product, cystic fibrosis transmembrane conductance regulator (CFTR), has widened the spectrum of the disease from the classical case of the infant with cystic fibrosis to the elderly childless man with unexplained bronchiectasis. There is increasing evidence of the advantages of newborn screening for cystic fibrosis and subsequent specialist care. Management concentrates on optimising nutritional status and preventing lung infection and inflammation." @default.
• W1907761738 created "2016-06-24" @default.
• W1907761738 creator A5076758255 @default.
• W1907761738 date "2001-07-01" @default.
• W1907761738 modified "2023-09-29" @default.
• W1907761738 title "Recent advances in cystic fibrosis" @default.
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• W1907761738 doi "https://doi.org/10.1136/adc.85.1.62" @default.
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