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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Detaylı Bibliyografya
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Publishing Group 2014
Konular:
Cystic Fibrosis
Online Erişim: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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