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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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| Publicat a: | J Int Med Res |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
SAGE Publications
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7683927/ https://ncbi.nlm.nih.gov/pubmed/33203284 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0300060520964378 |
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