The Potential Application and Promising Role of Targeted Therapy in Pulmonary Arterial Hypertension
Pulmonary arterial hypertension (PAH) is a rare yet serious progressive disorder that is currently incurable. This female-predominant disease unfolds as a pan-vasculopathy that affects all layers of the vessel wall. Five classes of pharmacological agents currently exist to target the three major cel...
Main Authors: | Meng-Chien Willie Hsieh, Wei-Ting Wang, Jwu-Lai Yeh, Chuang-Yu Lin, Yur-Ren Kuo, Su-Shin Lee, Ming-Feng Hou, Yi-Chia Wu |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-06-01
|
Series: | Biomedicines |
Subjects: | |
Online Access: | https://www.mdpi.com/2227-9059/10/6/1415 |
Similar Items
-
Perioperative Management of Pulmonary Hypertension. A Review
by: Wood Christopher, et al.
Published: (2021-05-01) -
Mitochondrial Dysfunction in Pulmonary Hypertension
by: Gusty Rizky Teguh Ryanto, et al.
Published: (2023-02-01) -
Muscle strength is reduced in children with pulmonary arterial hypertension
by: Shari Pepplinkhuizen, et al.
Published: (2023-04-01) -
New progress in diagnosis and treatment of pulmonary arterial hypertension
by: Zai-qiang Zhang, et al.
Published: (2022-08-01) -
Pulmonary Hypertension in Left Heart Diseases: Pathophysiology, Hemodynamic Assessment and Therapeutic Management
by: Zied Ltaief, et al.
Published: (2023-06-01)