Carcinoembryonic antigen levels are increased with pulmonary output in pulmonary hypertension due to congenital heart disease

OBJECTIVE: Pulmonary artery hypertension (PAH) is a severe complication of congenital heart disease (CHD). Monitoring of pulmonary arterial pressure (PAP) and pulmonary vascular resistance (PVR) is essential during follow-up. This retrospective study aimed to examine carcinoembryonic antigen (CEA) a...

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Detalles Bibliográficos
Autores principales: Zi-yang, Yang, Kaixun, Zhao, Dongling, Luo, Zhou, Yin, Chengbin, Zhou, Jimei, Chen, Caojin, Zhang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Retrospective Clinical Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683927/
https://www.ncbi.nlm.nih.gov/pubmed/33203284
http://dx.doi.org/10.1177/0300060520964378

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683927/
https://www.ncbi.nlm.nih.gov/pubmed/33203284
http://dx.doi.org/10.1177/0300060520964378

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