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Endpoints for Clinical Trials in Young Children with Cystic Fibrosis
The availability of sensitive, reproducible, and feasible outcome measures for quantifying lung disease in children with cystic fibrosis (CF) younger than 6 years is critical to the conduct of clinical trials in this important population. Historically, identifying and quantifying the presence of lun...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Thoracic Society
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2647606/ https://ncbi.nlm.nih.gov/pubmed/17652509 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1513/pats.200703-041BR |
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