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Analysis of a large cohort of cystic fibrosis patients with severe liver disease indicates lung function decline does not significantly differ from that of the general cystic fibrosis population
Previous reports of lung function in cystic fibrosis (CF) patients with liver disease have shown worse, similar, or even better forced expiratory volume in 1 second (FEV(1)), compared to CF patients without liver disease. Varying definitions of CF liver disease likely contribute to these inconsisten...
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| Vydáno v: | PLoS One |
|---|---|
| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6181334/ https://ncbi.nlm.nih.gov/pubmed/30307979 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0205257 |
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