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Circulating endothelial cells: A potential parameter of organ damage in sickle cell anemia?

โœ Scribed by Michiel H. Strijbos; Precious P. Landburg; Erfan Nur; Tom Teerlink; Frank W.G. Leebeek; Anita W. Rijneveld; Bart J. Biemond; Stefan Sleijfer; Jan W. Gratama; Ashley J. Duits; John-John B. Schnog


Book ID
116304673
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
497 KB
Volume
43
Category
Article
ISSN
1079-9796

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โœ Croizat, Helena; Nagel, Ronald L. ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 179 KB ๐Ÿ‘ 2 views

A hemoglobin F (HbF) level between eight and nine percent divides sickle cell anemia (SS) patients into two populations, according to the kinetics of circulating burst forming units-erythroid (BFU-E), long term culture-initialing cells (LTC-IC), and cytokine plasma concentrations. The SS patients wi