Macitentan in Pulmonary Arterial Hypertension Due to Congenital Heart Disease (CHD-PAH): Real-World Evidence from the OPUS/OrPHeUS Studies

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Publication Details

Journal
Cardiology and Therapy
Published
2024-11-25
DOI
https://doi.org/10.1007/s40119-024-00386-1
Citations
2
Primary Topic
Pulmonary Hypertension Research and Treatments
Type
article
Field-Weighted Citation Impact
0.84

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article

Macitentan in Pulmonary Arterial Hypertension Due to Congenital Heart Disease (CHD-PAH): Real-World Evidence from the OPUS/OrPHeUS Studies

Nick H. Kim, Stefano Turricchia, Vallerie V. McLaughlin, Richard N. Channick et al.
2 citations
Cardiology and Therapy
Pulmonary Hypertension Research and Treatments
0.84
article

Macitentan in Pulmonary Arterial Hypertension Due to Congenital Heart Disease (CHD-PAH): Real-World Evidence from the OPUS/OrPHeUS Studies

Nick H. Kim, Stefano Turricchia, Vallerie V. McLaughlin, Richard N. Channick, Kelly Chin, Nicolas Martin, Lada Mitchell, Rose Ong
article en
2 citations

Abstract

No abstract available for this paper.
Cardiology and TherapyVol. 13(4)
University of California, Los Angeles (US), University of Michigan (US), University of California San Diego (US), Johnson & Johnson (Switzerland) (CH), Southwestern Medical Center (US), Southwestern Medical Center (US), The University of Texas Southwestern Medical Center (US), Actelion (Switzerland) (CH)
Actelion Pharmaceuticals
Good health and well-being
Openalex Percentile: Top 23%
Pulmonary Hypertension Research and Treatments
0.84
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