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pro vyhledávání: '"Chinwuwanuju Ugo‐Obi Sampson"'
Publikováno v:
Pulmonary Circulation, Vol 13, Iss 4, Pp n/a-n/a (2023)
Abstract Pulmonary arterial hypertension (PAH) is a rare, complex, and deadly cardiopulmonary disease. It is characterized by changes in endothelial cell function and smooth muscle cell proliferation in the pulmonary arteries, causing persistent vaso
Externí odkaz:
https://doaj.org/article/b7a483237cff48d19a4e3a0e9c6fdd9b