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Ambrisentan for the treatment of pulmonary arterial hypertension: improving outcomes

Pulmonary arterial hypertension (PAH) is a progressive disease of the pulmonary vasculature that is associated with severe functional impairment and a poor prognosis. Ambrisentan is a selective endothelin type A receptor antagonist approved for the treatment of patients with PAH World Health Organiz...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Elshaboury, Soha M, Anderson, Joe R
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Dove Medical Press 2013
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3652514/
https://ncbi.nlm.nih.gov/pubmed/23674888
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/PPA.S30949
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