从肺动脉高压形成的病理生理机制看阿司匹林治疗的可能性
被引量:4
摘要
肺动脉高压(pulmonary artefial hypertension,PAH)是一种危及生命的疾病,其特点是肺动脉压力和肺血管阻力进行性升高,最终导致右心衰竭和死亡。
出处
《中国心血管杂志》
2010年第6期479-481,共3页
Chinese Journal of Cardiovascular Medicine
基金
上海市卫生局科研课题项目资助(2007103)
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