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Endothelin Receptor Antagonists are an Effective Long Term Treatment Option in Pulmonary Arterial Hypertension Associated with Congenital Heart Disease With or Without Trisomy 21
Authors:F.D. Kermeen,C. Franks,K. O&rsquo  Brien,H. Seale,K. Hall,K. McNeil,D. Radford
Affiliation:1. The Queensland Centre for Pulmonary Transplantation and Vascular Disease, The Prince Charles Hospital, Brisbane, Queensland, Australia;2. The Adult Congenital Heart Disease Unit, The Prince Charles Hospital, Brisbane, Queensland, Australia
Abstract:
Keywords:Endothelin receptor antagonists   Eisenmenger syndrome   Trisomy 21
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