Articles
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Oct 5, 2023 |
acrjournals.onlinelibrary.wiley.com | Tatsuya Atsumi |Sang-Cheol Bae |Hong Gu |Wen-Nan Huang
INTRODUCTION Pulmonary arterial hypertension (PAH) is a rare, progressive, and severe cardiopulmonary disorder (1). In patients with PAH, the small pulmonary arteries are obstructed because of cellular proliferation, fibrosis, and vascular remodeling, leading to premature death from right-sided heart failure (2-4).
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