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pro vyhledávání: '"Taha Hashim Ahmed"'
Publikováno v:
Al-Mustansiriyah Journal of Pharmaceutical Sciences, Vol 24, Iss 3 (2024)
Pulmonary arterial hypertension (PAH) is a chronic, rare, and non-treatable disease, resulting in elevated mean arterial pressure (≥25mmHg) during rest and (≥30mmHg) during exercise. Pulmonary arteries remodeling including endothelial apoptosi
Externí odkaz:
https://doaj.org/article/dd75a0e1b6b94f73999f9e1843b5e311
