Although the values did not reach statistical significance, patients with sJIA and anemia trended toward higher percentages of CD34 + cell subpopulations than did patients with sJIA without anemia, suggesting that the expansion of these immature PBMC subpopulations was rather specific to individuals with sJIA and anemia.
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Immature cell populations and an erythropoiesis gene-expression signature in systemic juvenile idiopathic arthritis: implications for pathogenesis.
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