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- W4293496078 abstract "Abstract Pulmonary arterial hypertension (PAH) is a progressive disease. Although great progress has been made in its diagnosis and treatment in recent years, its mortality rate is still very significant. The pathophysiology and pathogenesis of PAH are complex and involve endothelial dysfunction, chronic inflammation, smooth muscle cell proliferation, pulmonary arteriole occlusion, antiapoptosis and pulmonary vascular remodeling. These factors will accelerate the progression of the disease, leading to poor prognosis. Therefore, accurate etiological diagnosis, treatment and prognosis judgment are particularly important. Here, we systematically review the pathophysiology, diagnosis, genetics, prognosis and treatment of PAH." @default.
- W4293496078 created "2022-08-29" @default.
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- W4293496078 date "2022-08-29" @default.
- W4293496078 modified "2023-10-16" @default.
- W4293496078 title "New progress in diagnosis and treatment of pulmonary arterial hypertension" @default.
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- W4293496078 doi "https://doi.org/10.1186/s13019-022-01947-y" @default.
- W4293496078 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36038916" @default.
- W4293496078 hasPublicationYear "2022" @default.
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