Pathophysiology and Treatment of Pulmonary Arterial Hypertension
Author:
Affiliation:
1. Division of Cardiovascular Medicine, Department of Internal Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan
Abstract
Publisher
MDPI AG
Link
https://www.mdpi.com/1422-0067/25/2/1166/pdf
Reference16 articles.
1. Guidelines for the Treatment of Pulmonary Hypertension (JCS 2017/JPCPHS 2017);Fukuda;Circ. J.,2019
2. 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension;Humbert;Eur. Heart J.,2022
3. Pulmonary artery distensibility index is a non-invasive useful marker of pulmonary arterial hypertension progression;Fukumoto;Circ. J.,2011
4. Intensive immunosuppressive therapy improves pulmonary hemodynamics and long-term prognosis in patients with pulmonary arterial hypertension associated with connective tissue disease;Fukumoto;Circ. J.,2011
5. Histopathological examination by lung biopsy for the evaluation of operability and postoperative prognosis in patients with chronic thromboembolic pulmonary hypertension;Yamaki;Circ. J.,2014
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