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Cystic fibrosis: terminology and diagnostic algorithms
There is great heterogeneity in the clinical manifestations of cystic fibrosis (CF). Some patients may have all the classical manifestations of CF from infancy and have a relatively poor prognosis, while others have much milder or even atypical disease manifestations and still carry mutations on eac...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Group
2006
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2104676/ https://ncbi.nlm.nih.gov/pubmed/16384879 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thx.2005.043539 |
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