Circulating Endothelial Progenitor Cells and Their Relation to Thrombosis in Paroxysmal Nocturnal Hemoglobinuria and Aplastic Anemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
https://link.springer.com/content/pdf/10.1007/s12288-021-01445-6.pdf
Reference29 articles.
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2. Yenerel MN, Muus P, Wilson A, Szer J (2017) Clinical course and disease burden in patients with paroxysmal nocturnal hemoglobinuria by hemolytic status. Blood Cells Mol Dis 65:29–34
3. Nicholson-Weller A, Spicer DB, Austen KF (1985) Deficiency of the complement regulatory protein, “decay-accelerating factor”, on membranes of granulocytes, monocytes, and platelets in paroxysmal nocturnal hemoglobinuria. N Engl J Med 312(17):1091
4. Griscelli-Bennaceur A, Gluckman E, Scrobohaci ML et al (1995) Aplastic anemia and paroxysmal nocturnal hemoglobinuria: search for a pathogenetic link. Blood 85(1354):67
5. Schubert J, Vogt HG, Zielinska-Skowronek M et al (1994) Development of the glycosylphosphatitylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia. Blood 83:2323
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