The Impact of Pulmonary Arterial Pressure on Exercise Capacity in Mild-to-Moderate Cystic Fibrosis: A Case Control Study

Background. Pulmonary hypertension (PH) is an often complication of severe cystic fibrosis (CF); however, data on the presence and impact of pulmonary vasculopathy in adult CF patients with milder disease, is very limited. Aim. To investigate, for the first time, the impact of systolic pulmonary art...

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Bibliografische gegevens
Hoofdauteurs: Manika, Katerina, Pitsiou, Georgia G., Boutou, Afroditi K., Tsaoussis, Vassilis, Chavouzis, Nikolaos, Antoniou, Marina, Fotoulaki, Maria, Stanopoulos, Ioannis, Kioumis, Ioannis
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Hindawi Publishing Corporation 2012
Onderwerpen:
Clinical Study
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3414060/
https://ncbi.nlm.nih.gov/pubmed/22900167
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/252345
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