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Science 3 September 1976:
Vol. 193. no. 4256, pp. 899 - 900
DOI: 10.1126/science.986086
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Articles

Science, Vol 193, Issue 4256, 899-900
Copyright © 1976 by American Association for the Advancement of Science

articles

Diamond-Blackfan syndrome: lymphocyte-mediated suppression of erythropoiesis

R Hoffman, ED Zanjani, J Vila, R Zalusky, JD Lutton, and LR Wasserman

Peripheral blood lymphocytes from six patients with congenital hypoplastic anemia suppressed erythroid cell formation by normal human bone marrow cells in response to erythropoietin in vitro. The results suggest that the anemia in these children has an immunologic basis.


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Elevation of the Serum Fas Ligand in Patients With Hemophagocytic Syndrome and Diamond-Blackfan Anemia.
D. Hasegawa, S. Kojima, E. Tatsumi, A. Hayakawa, Y. Kosaka, H. Nakamura, M. Sako, Y. Osugi, S. Nagata, and K. Sano (1998)
Blood 91, 2793-2799
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Multiple Congenital Anomalies in a Patient with Diamond-Blackfan Syndrome.
K. H. Lazarus and F. A. McCurdy (1984)
Clinical Pediatrics 23, 520-522
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Aplastic Anemia: Biology and Treatment.
R. P. GALE, R. E. CHAMPLIN, S. A. FEIG, and J. H. FITCHEN (1981)
Ann Intern Med 95, 477-494
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Transient Pure Red-Cell Aplasia: Cell-Mediated Suppression of Erythropoiesis Associated with Hepatitis.
H. A. WILSON, G. D. McLAREN, H. J. DWORKEN, and K. TEBBI (1980)
Ann Intern Med 92, 196-198
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