期刊
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
卷 177, 期 6, 页码 574-579出版社
AMER THORACIC SOC
DOI: 10.1164/rccm.200801-029UP
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This article summarizes recent advances in the field of pulmonary arterial hypertension (PAH), a severe condition characterized by a progressive remodeling of small pulmonary arteries leading to elevated pulmonary vascular resistance and right ventricular failure (1, 2). Epidemiology, genetics, pathophysiology, and treatment will be the main focus of this update.
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