The majority of patients with cystic fibrosis (CF) will grow into adulthood. Despite this improvement in survival, the disease is progressive, especially with respect to the decline in pulmonary function, which in turn may have an impact on a patient's quality of life. In this study we evaluated the
Overall and peripheral inhomogeneity of ventilation in patients with stable cystic fibrosis
β Scribed by Alain Van Muylem; D. Baran
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 106 KB
- Volume
- 30
- Category
- Article
- ISSN
- 8755-6863
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