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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BMJ Publishing Group 2014
Pynciau:
Cystic Fibrosis
Mynediad Ar-lein: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
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg