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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Cystic Fibrosis
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963531/
https://www.ncbi.nlm.nih.gov/pubmed/24132911
http://dx.doi.org/10.1136/thoraxjnl-2013-204176

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963531/
https://www.ncbi.nlm.nih.gov/pubmed/24132911
http://dx.doi.org/10.1136/thoraxjnl-2013-204176

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