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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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Podrobná bibliografie
Vydáno v:J Int Med Res
Hlavní autoři: Zi-yang, Yang, Kaixun, Zhao, Dongling, Luo, Zhou, Yin, Chengbin, Zhou, Jimei, Chen, Caojin, Zhang
Médium: Artigo
Jazyk:Inglês
Vydáno: SAGE Publications 2020
Témata:
On-line přístup: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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