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Pharmacotherapy for pulmonary arterial hypertension
Pulmonary arterial hypertension (PAH) is a condition associated with substantial morbidity and mortality. Over the last 25 years there has been a significant evolution in the therapies to treat PAH. These therapies are effective for patients with group I PAH and group IV PH [chronic thromboembolic p...
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| Udgivet i: | J Thorac Dis |
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| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
AME Publishing Company
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6783726/ https://ncbi.nlm.nih.gov/pubmed/31632754 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/jtd.2019.09.14 |
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