Optical characterization of red blood cells from individuals with sickle cell trait and disease in Tanzania using quantitative phase imaging-Reference-Cited by-同舟云学术

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Optical characterization of red blood cells from individuals with sickle cell trait and disease in Tanzania using quantitative phase imaging

Published:2016-08 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Jung JaeHwang,Matemba Lucas E.,Lee KyeoReh,Kazyoba Paul E.,Yoon Jonghee,Massaga Julius J.,Kim Kyoohyun,Kim Dong-Jin,Park YongKeun

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep31698.pdf

Reference60 articles.

1. Pauling, L., Itano, H. A., Singer, S. & Wells, I. C. Sickle cell anemia, a molecular disease. Science 110, 543–548 (1949).

2. Stuart, M. J. & Nagel, R. L. Sickle-cell disease. The Lancet 364, 1343–1360 (2004).

3. PediatriaAshley-Koch, A., Yang, Q. & Olney, R. S. Sickle hemoglobin (Hb S) allele and sickle cell disease: a HuGE review. American Journal of Epidemiology 151, 839–845 (2000).

4. Roseff, S. Sickle cell disease: a review. Immunohematology/American Red Cross 25, 67–74 (2008).

5. Kark, J. A., Posey, D. M., Schumacher, H. R. & Ruehle, C. J. Sickle-cell trait as a risk factor for sudden death in physical training. New England Journal of Medicine 317, 781–787 (1987).

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