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Pulmonary Arterial Hypertension Diagnosis, Treatment, and Clinical Management in the Contemporary Era
IMPORTANCE: Pulmonary arterial hypertension (PAH) is characterized by severe remodeling of distal pulmonary arteries, increased pulmonary vascular resistance and right ventricular dysfunction that promotes heart failure. Once regarded as largely untreatable, evidence-based decision-making now guides...
Tallennettuna:
| Julkaisussa: | JAMA Cardiol |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5177491/ https://ncbi.nlm.nih.gov/pubmed/27851839 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamacardio.2016.4471 |
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