Is chest CT useful in newborn screened infants with cystic fibrosis at 1 year of age?

RATIONALE: Sensitive outcome measures applicable in different centres to quantify and track early pulmonary abnormalities in infants with cystic fibrosis (CF) are needed both for clinical care and interventional trials. Chest CT has been advocated as such a measure yet there is no validated scoring...

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Opis bibliograficzny
Główni autorzy: Thia, Lena P, Calder, Alistair, Stocks, Janet, Bush, Andrew, Owens, Catherine M, Wallis, Colin, Young, Carolyn, Sullivan, Yvonne, Wade, Angie, McEwan, Angus, Brody, Alan S
Format: Artigo
Język:Inglês
Wydane: BMJ Publishing Group 2014
Hasła przedmiotowe:
Cystic Fibrosis
Dostęp online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3963531/
https://ncbi.nlm.nih.gov/pubmed/24132911
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thoraxjnl-2013-204176
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