التفاصيل البيبلوغرافية
| العنوان: |
Idiopathic Pulmonary Fibrosis: Best Practice in Monitoring and Managing a Relentless Fibrotic Disease |
| المؤلفون: |
Wuyts, W. A., Wijsenbeek, M., Bondue, B., Bouros, D., Bresser, P., Cordeiro, C. R., Hilberg, O., Magnusson, Jesper, Manali, E. D., Morais, A., Papiris, S., Shaker, S., Veltkamp, M., Bendstrup, E. |
| المصدر: |
Respiration. 99(1):73-82 |
| مصطلحات موضوعية: |
Clinical Medicine, Klinisk medicin, Nintedanib, Pirfenidone, Interstitial lung disease, Therapeutics, Treatment, Mortality, forced vital capacity, quality-of-life, clinical-practice, acute, exacerbation, lung-transplant, antacid therapy, home spirometry, palliative care, position paper, survival, Respiratory System |
| الوصف: |
Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial lung disease that is, by definition |
| URL الوصول: |
https://gup.ub.gu.se/publication/290618 |
| قاعدة البيانات: |
SwePub |
