The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
Management of Sickle Cell Disease
Abstract
One of every 600 black people in the United States has sickle cell anemia. In addition, sickle cell–hemoglobin C disease and sickle cell–β-thalassemia, which are other common genotypes of sickle cell disease, together are as common as sickle cell anemia. Sickle hemoglobin (hemoglobin S, α2 β2S) accounts for over half the hemoglobin in patients with these disorders. Eight percent of black Americans are heterozygous carriers of the sickle cell trait; about 40 percent of their hemoglobin is hemoglobin S. They do not have anemia and need neither treatment nor occupational restrictions. About 5 percent have hematuria at . . .
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Cites
Mortality in sickle cell disease. Life expectancy and risk factors for early death
Platt, O. S., Brambilla, D. J., Rosse, W. F., Milner, P. F., Castro, O., Steinberg, M. H., & Klug, P. P. (1994) · New England Journal of Medicine · doi:10.1056/nejm199406093302303 · Cited by 3,320
Self-citationEffect of hydroxyurea on the frequency of painful crises in sickle cell anemia
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Pain in Sickle Cell Disease: Rates and Risk Factors
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Pathogenesis and Treatment of Sickle Cell Disease
Bunn, H. F. (1997) · New England Journal of Medicine · doi:10.1056/nejm199709113371107 · Cited by 1,154
Acute Chest Syndrome in Sickle Cell Disease: Clinical Presentation and Course
Vichinsky, E. P., Styles, L. A., Colangelo, L. H., Wright, E. C., Castro, O., Nickerson, B., & Disease, T. C. S. O. S. C. (1997) · Blood · doi:10.1182/blood.v89.5.1787 · Cited by 573
Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea
Steinberg, M. H., Lu, Z.-H., Barton, F. B., Terrin, M. L., Charache, S., Dover, G. J., & Hydroxyurea, T. M. S. O. (1997) · Blood · doi:10.1182/blood.v89.3.1078 · Cited by 407
Self-citation5-Azacytidine stimulates fetal hemoglobin synthesis in anemic baboons.
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A multiparameter analysis of sickle erythrocytes in patients undergoing hydroxyurea therapy
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Cited by
Stuart, M. J., & Nagel, R. L. (2004) · The Lancet · doi:10.1016/s0140-6736(04)17192-4 · Cited by 819
Thomson, A. M., McHugh, T. A., Oron, A. P., Teply, C., Lonberg, N., Vilchis Tella, V., Wilner, L. B., Fuller, K., Hagins, H., Aboagye, R. G., et al. (2023) · The Lancet Haematology · doi:10.1016/s2352-3026(23)00118-7 · Cited by 747
The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: a 17.5 year follow-up
Steinberg, M. H., McCarthy, W. F., Castro, O., Ballas, S. K., Armstrong, F. D., Smith, W., Ataga, K., Swerdlow, P., Kutlar, A., DeCastro, L., et al. (2010) · American Journal of Hematology · doi:10.1002/ajh.21699 · Cited by 486
Self-citationPulmonary Complications of Sickle Cell Disease
Gladwin, M. T., & Vichinsky, E. (2008) · New England Journal of Medicine · doi:10.1056/nejmra0804411 · Cited by 470
A systematic review of sleep in pediatric pain populations
Valrie, C. R., Bromberg, M. H., Palermo, T., & Schanberg, L. E. (2013) · Journal of Developmental & Behavioral Pediatrics · doi:10.1097/dbp.0b013e31827d5848 · Cited by 237
Metadata
- Authors
- Steinberg, M. H.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 1999-04
- Volume
- 340
- Issue
- 13
- Pages
- 1021-1030
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2322453619
- Cited by
- 604
- References
- 9
- FWCI
- 18.15
- Type
- journal article
- Language
- en
- Open access
- closed
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
