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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Detaylı Bibliyografya
Asıl Yazarlar: De Boeck, K, Wilschanski, M, Castellani, C, Taylor, C, Cuppens, H, Dodge, J, Sinaasappel, M
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Group 2006
Konular:
Occasional Review
Online Erişim: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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