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Severe pulmonary hypertension in idiopathic nonspecific interstitial pneumonia
Pulmonary hypertension (PH) is a common complication of interstitial lung disease (ILD), particularly in idiopathic pulmonary fibrosis (IPF) and ILD associated with connective tissue disease, where the underlying pathology is often a nonspecific interstitial pneumonia (NSIP) pattern. The degree of P...
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| Glavni autori: | , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Medknow Publications & Media Pvt Ltd
2012
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3342738/ https://ncbi.nlm.nih.gov/pubmed/22558525 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2045-8932.94842 |
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