Endothelin receptor antagonists for pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a consequence of acute or chronic disorder of the pulmonary vasculature, which is characterized by increased pulmonary artery pressure as a result of increased pulmonary vascular resistance. The pathophysiology of PAH is characterized by pulmonary vascular va...

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Detalles Bibliográficos
Autores principales: Bevacqua, R.J., Bortman, G., Perrone, S.V.
Formato: JOUR
Materias:
Ambrisentan
Bosentan
Combination therapy
Endothelin receptor antagonist
Pathophysiological pathways
Pulmonary arterial hypertension
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_18501044_v8_n2_p77_Bevacqua
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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