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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Dettagli Bibliografici
Autori principali: Manika, Katerina, Pitsiou, Georgia G., Boutou, Afroditi K., Tsaoussis, Vassilis, Chavouzis, Nikolaos, Antoniou, Marina, Fotoulaki, Maria, Stanopoulos, Ioannis, Kioumis, Ioannis
Natura: Artigo
Lingua:Inglês
Pubblicazione: Hindawi Publishing Corporation 2012
Soggetti:
Clinical Study
Accesso online: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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