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MMPs, inflammation and pulmonary arterial hypertension
Pulmonary arterial hypertension (PAH) is characterised by remodelling of small pulmonary arteries leading to a progressive increase in pulmonary vascular resistance and right ventricular failure [1]. PAH can be idiopathic, familial, or associated with a number of conditions or diseases, such as conn...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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2008
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7122977/ http://dx.doi.org/10.1007/978-3-7643-8585-9_6 |