The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Managing sickle cell disease
Open accessAbstract
Advances are being made in the management of sickle cell disease for all age groups. This review discusses the progress in amelioration of symptoms, problems unique to particular age groups, and the types of drugs and treatments currently under investigation
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Citations
Cites
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia
Charache, S., Terrin, M. L., Moore, R. D., Dover, G. J., Barton, F. B., Eckert, S. V., McMahon, R. P., & Bonds, D. R. (1995) · New England Journal of Medicine · doi:10.1056/nejm199505183322001 · Cited by 2,340
Pain in Sickle Cell Disease: Rates and Risk Factors
Platt, O. S., Thorington, B. D., Brambilla, D. J., Milner, P. F., Rosse, W. F., Vichinsky, E., & Kinney, T. R. (1991) · New England Journal of Medicine · doi:10.1056/nejm199107043250103 · Cited by 1,546
Self-citationCauses and Outcomes of the Acute Chest Syndrome in Sickle Cell Disease
Vichinsky, E. P., Neumayr, L. D., Earles, A. N., Williams, R., Lennette, E. T., Dean, D., Nickerson, B., Orringer, E., McKie, V., Bellevue, R., et al. (2000) · New England Journal of Medicine · doi:10.1056/nejm200006223422502 · Cited by 1,234
Self-citationAcute 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
Self-citationPrediction of Adverse Outcomes in Children with Sickle Cell Disease
Miller, S. T., Sleeper, L. A., Pegelow, C. H., Enos, L. E., Wang, W. C., Weiner, S. J., Wethers, D. L., Smith, J., & Kinney, T. R. (2000) · New England Journal of Medicine · doi:10.1056/nejm200001133420203 · Cited by 508
Cited by
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
Szczepiorkowski, Z. M., Winters, J. L., Bandarenko, N., Kim, H. C., Linenberger, M. L., Marques, M. B., Sarode, R., Schwartz, J., Weinstein, R., & Shaz, B. H. (2010) · Journal of Clinical Apheresis · doi:10.1002/jca.20240 · Cited by 508
Management of sickle cell disease from childhood through adulthood
Kanter, J., & Kruse-Jarres, R. (2013) · Blood Reviews · doi:10.1016/j.blre.2013.09.001 · Cited by 182
Keller, S. D., Yang, M., Treadwell, M. J., Werner, E. M., & Hassell, K. L. (2014) · Health and Quality of Life Outcomes · doi:10.1186/s12955-014-0125-0 · Cited by 115
Amujoyegbe, O. O., Idu, M., Agbedahunsi, J. M., & Erhabor, J. O. (2016) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2016.03.042 · Cited by 66
Metadata
- Authors
- Claster, S., & Vichinsky, E. P.
- Venue
- BMJ
- Publisher
- BMJ
- Published
- 2003-11-13
- Volume
- 327
- Issue
- 7424
- Pages
- 1151-1155
- ISSN
- 0007-1447 (ISSN-L)
- 0959-8138
- 1468-5833
- OpenAlex
- W2031039743
- Cited by
- 198
- References
- 5
- FWCI
- 3.44
- Type
- journal article
- Language
- en
- Open access
- green
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- Claster, S., & Vichinsky, E. P. (2003). Managing sickle cell disease. BMJ. https://doi.org/10.1136/bmj.327.7424.1151
Data sources
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.
