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Published in 2018 at "European Journal of Immunology"
DOI: 10.1002/eji.201747460
Abstract: Idiopathic pulmonary arterial hypertension (IPAH) is a devastating pulmonary vascular disease in which autoimmune and inflammatory phenomena are implicated. B cells and autoantibodies have been associated with IPAH and identified as potential therapeutic targets. However,…
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Keywords:
idiopathic pulmonary;
arterial hypertension;
endothelial cell;
pulmonary arterial ... See more keywords