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Pulmonary Arterial Hypertension: Pathophysiology and Treatment
Pulmonary arterial hypertension (PAH), the first category of pulmonary hypertension, is a chronic and progressive disorder characterised by angioproliferative vasculopathy in the pulmonary arterioles, leading to endothelial and smooth muscle proliferation and dysfunction, inflammation and thrombosis...
Kaydedildi:
| Yayımlandı: | Diseases |
|---|---|
| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
MDPI
2018
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6023499/ https://ncbi.nlm.nih.gov/pubmed/29772649 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diseases6020038 |
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