Nationwide lung function monitoring from infancy in newborn-screened children with cystic fibrosis

BACKGROUND: Cystic fibrosis (CF) lung disease starts in infancy and can be assessed for structural lung abnormalities using computed tomography or magnetic resonance scans, or for lung function impairment using multiple breath washout (MBW). However, in infancy these two methods are not well correla...

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Detalles Bibliográficos
Autores principales: Sandvik, Rikke M., Schmidt, Marika N., Voldby, Christian M., Buchvald, Frederik F., Olesen, Hanne V., Olsen, Jørgen, Kragh, Maja V., Rubak, Sune L.M., Pressler, Tacjana, Robinson, Paul D., Gustafsson, Per M., Skov, Marianne, Nielsen, Kim G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2023
Materias:
Original Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10613974/
https://www.ncbi.nlm.nih.gov/pubmed/37908398
http://dx.doi.org/10.1183/23120541.00317-2023

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10613974/
https://www.ncbi.nlm.nih.gov/pubmed/37908398
http://dx.doi.org/10.1183/23120541.00317-2023

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