Adenosine Receptors As Drug Targets for Treatment of Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a clinical condition characterized by pulmonary arterial remodeling and vasoconstriction, which promote chronic vessel obstruction and elevation of pulmonary vascular resistance. Long-term right ventricular (RV) overload leads to RV dysfunction and failure, w...

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Bibliographic Details
Main Authors: Allan K. N. Alencar (Author), Guilherme C. Montes (Author), Eliezer J. Barreiro (Author), Roberto T. Sudo (Author), Gisele Zapata-Sudo (Author)
Format: Book
Published: Frontiers Media S.A., 2017-12-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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