High-Resolution Computed Tomography Imaging of Airway Disease in Infants with Cystic Fibrosis

Rationale: The development of early lung disease in patients with cystic fibrosis (CF) remains poorly defined. Objective: Determine whether asymptomatic infants with CF have evidence for changes in airway structure when assessed by high-resolution computed tomography, and whether airway structure co...

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Hlavní autoři: Martínez, Tanya M., Llapur, Conrado J., Williams, Tamica H., Coates, Cathy, Gunderman, Richard, Cohen, Mervyn D., Howenstine, Michelle S., Saba, Osama, Coxson, Harvey O., Tepper, Robert S.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Thoracic Society 2005
Témata:
D. Cystic Fibrosis
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2718397/
https://ncbi.nlm.nih.gov/pubmed/16051903
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.200412-1665OC
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