Cargando…
Lung function over the life course of paediatric and adult patients with cystic fibrosis from a large multi-centre registry
A key measure of lung function in people with Cystic Fibrosis (CF) is Forced Expiratory Volume in the first second FEV(1) percent predicted (FEV(1)pp). This study aimed to address challenges in identifying predictors of FEV(1)pp, specifically dealing with non-linearity and the censoring effect of de...
Autores principales: | Earnest, Arul, Salimi, Farhad, Wainwright, Claire E., Bell, Scott C., Ruseckaite, Rasa, Ranger, Tom, Kotsimbos, Tom, Ahern, Susannah |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567842/ https://www.ncbi.nlm.nih.gov/pubmed/33060788 http://dx.doi.org/10.1038/s41598-020-74502-1 |
Ejemplares similares
-
Survival of people with cystic fibrosis in Australia
por: Ruseckaite, Rasa, et al.
Publicado: (2022) -
Acceptability of patient reported outcome measures (PROMs) in a cystic fibrosis data registry
por: Ratnayake, Irushi, et al.
Publicado: (2021) -
A systematic review of patient-reported outcome measures (PROMs) in cystic fibrosis
por: Ratnayake, Irushi, et al.
Publicado: (2020) -
Patient-Reported Outcome Measures in Cystic Fibrosis: Protocol for a Systematic Review
por: Ratnayake, Irushi, et al.
Publicado: (2020) -
Hereditary Endocrine Tumor Registries
por: Moore, Edwina C, et al.
Publicado: (2022)