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Published in 2022 at "International Journal of Molecular Sciences"
DOI: 10.3390/ijms23126508
Abstract: Pulmonary arterial hypertension (PAH) is rare disease that is categorized as idiopathic (IPAH) when no underlying cause can be identified. Lungs of most patients with IPAH contain increased numbers of T cells and dendritic cells…
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Keywords:
ipah;
reduced cytokine;
peripheral blood;
ipah patients ... See more keywords