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Surrogate End Points in Pulmonary Arterial Hypertension: Assessing the Response to Therapy
Pulmonary arterial hypertension (PAH) is a rare disease which is characterized by increased pulmonary vascular resistance and right heart failure. Recent discoveries in disease pathophysiology have been translated into effective therapies tested in clinical trials. The studies which have led to the...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2007
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1868503/ https://ncbi.nlm.nih.gov/pubmed/17338929 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ccm.2006.11.005 |
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