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Beta‐blockers for preventing aortic dissection in Marfan syndrome
BACKGROUND: Marfan syndrome is a hereditary disorder affecting the connective tissue and is caused by a mutation of the fibrillin‐1 (FBN1) gene. It affects multiple systems of the body, most notably the cardiovascular, ocular, skeletal, dural and pulmonary systems. Aortic root dilatation is the most...
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| Publicado no: | Cochrane Database Syst Rev |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley & Sons, Ltd
2017
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6486285/ https://ncbi.nlm.nih.gov/pubmed/29110304 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD011103.pub2 |
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