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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: De Boeck, K, Wilschanski, M, Castellani, C, Taylor, C, Cuppens, H, Dodge, J, Sinaasappel, M
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMJ Group 2006
Aiheet:
Linkit: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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