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The objectives of this study were to determine the prevalence and characteristics of cough in idiopathic pulmonary fibrosis (IPF), chronic hypersensitivity pneumonitis (HP) and systemic sclerosis‐associated interstitial lung disease (SSc‐ILD). Click to show full abstract
The objectives of this study were to determine the prevalence and characteristics of cough in idiopathic pulmonary fibrosis (IPF), chronic hypersensitivity pneumonitis (HP) and systemic sclerosis‐associated interstitial lung disease (SSc‐ILD).
Keywords:
sclerosis associated;
lung disease;
interstitial lung;
systemic sclerosis;
associated interstitial;
lung
Journal Title: Respirology
Year Published: 2017
Link to full text (if available)
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Journal Title: Respirology
Year Published: 2017
Link to full text (if available)
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recommendations!