Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea-Reference-Cited by-同舟云学术

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Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea

Published:2007-02-13 Issue:6 Volume:7 Page:386-394
ISSN:1470-269X
Container-title:The Pharmacogenomics Journal
language:en
Short-container-title:Pharmacogenomics J

Author:

Ma Q,Wyszynski D F,Farrell J J,Kutlar A,Farrer L A,Baldwin C T,Steinberg M H

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology,Genetics,Molecular Medicine

Link

http://www.nature.com/articles/6500433.pdf

Reference49 articles.

1. Poillon WN, Kim BC, Rodgers GP, Noguchi CT, Schechter AN . Sparing effect of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S at physiologic ligand saturations. Proc Natl Acad Sci USA 1993; 90: 5039–5043.

2. Milner PF, Kraus AP, Sebes JI, Sleeper LA, Dukes KA, Embury SH et al. Sickle cell disease as a cause of osteonecrosis of the femoral head. N Engl J Med 1991; 325: 1476–1481.

3. Castro O, Brambilla DJ, Thorington B, Reindorf CA, Scott RB, Gillette P et al. The acute chest syndrome in sickle cell disease: incidence and risk factors. The cooperative study of sickle cell disease. Blood 1994; 84: 643–649.

4. Platt OS, Thorington BD, Brambilla DJ, Milner PF, Rosse WF, Vichinsky E et al. Pain in sickle cell disease-rates and risk factors. N Engl J Med 1991; 325: 11–16.

5. Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH et al. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med 1994; 330: 1639–1644.

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