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Impaired cardiac and peripheral hemodynamic responses to inhaled β(2)-agonist in cystic fibrosis
BACKGROUND: Pulmonary system dysfunction is a hallmark of cystic fibrosis (CF) disease. In addition to impaired cystic fibrosis transmembrane conductance regulator protein, dysfunctional β(2)-adrenergic receptors (β(2)AR) contribute to low airway function in CF. Recent observations suggest CF may al...
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| Pubblicato in: | Respir Res |
|---|---|
| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4560914/ https://ncbi.nlm.nih.gov/pubmed/26341519 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12931-015-0270-y |
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