Adenosine Receptors As Drug Targets for Treatment of Pulmonary Arterial Hypertension

• Κύριοι συγγραφείς: Allan K. N. Alencar (Συγγραφέας), Guilherme C. Montes (Συγγραφέας), Eliezer J. Barreiro (Συγγραφέας), Roberto T. Sudo (Συγγραφέας), Gisele Zapata-Sudo (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: Frontiers Media S.A., 2017-12-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: Connect to this object online.

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...