Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 3 September 1976:
Vol. 193. no. 4256, pp. 899 - 900
DOI: 10.1126/science.986086
Prev | Table of Contents | Next

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.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
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
   Abstract »    Full Text »    PDF »
Multiple Congenital Anomalies in a Patient with Diamond-Blackfan Syndrome.
K. H. Lazarus and F. A. McCurdy (1984)
Clinical Pediatrics 23, 520-522
   PDF »
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
   Abstract »    PDF »
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
   Abstract »    PDF »


To Advertise     Find Products

Science. ISSN 0036-8075 (print), 1095-9203 (online)