Manual article review is required for this article
Manual article review is required for this article
Manual article review is required for this article
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Pulmonary Arterial Hypertension (PAH) presents a formidable challenge within the realm of cardiovascular drugs, characterised by elevated blood pressure in the arteries from the lungs, leading to progressive right coronary heart failure and decreased training tolerance. While regular therapies have centered on pharmacological interventions, rising
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