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Discovery of a Murine Model of Clinical PAH: Mission Impossible?
Pulmonary arterial hypertension (PAH) is a lung vascular disease characterized with a progressive increase of pulmonary vascular resistance and obliterative pulmonary vascular remodeling resulting in right heart failure and premature death. In this brief review, we document the recent advances in id...
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| Publicado no: | Trends Cardiovasc Med |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5400690/ https://ncbi.nlm.nih.gov/pubmed/28089339 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tcm.2016.12.003 |
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