The clinical presentation, utilization, and outcome of individuals with sickle cell anaemia presenting to urban emergency department of a tertiary hospital in Tanzania-Reference-Cited by-同舟云学术

The clinical presentation, utilization, and outcome of individuals with sickle cell anaemia presenting to urban emergency department of a tertiary hospital in Tanzania

Published:2018-09-17 Issue:1 Volume:18 Page:
ISSN:2052-1839
Container-title:BMC Hematology
language:en
Short-container-title:BMC Hematol

Author:

Sawe Hendry R.,Reynolds Teri A.,Mfinanga Juma A.,Runyon Michael S.,Murray Brittany L.,Wallis Lee A.,Makani Julie

Funder

Fogarty International Center

Publisher

Springer Science and Business Media LLC

Subject

Hematology,Molecular Biology

Link

http://link.springer.com/content/pdf/10.1186/s12878-018-0122-3.pdf

Reference24 articles.

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2. 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(23):1639–44.

3. Weatherall DJ. The inherited diseases of hemoglobin are an emerging global health burden. Blood. 2010;115(22):4331–6.

4. Fleming AF. The presentation, management and prevention of crisis in sickle cell disease in Africa. Blood Rev. 1989;3(1):18–28.

5. Oniyangi O, Omari AA. Malaria chemoprophylaxis in sickle cell disease. In: Cochrane Database of Systematic Reviews [Internet]. John Wiley & Sons, Ltd; 1996 [cited 2013 Mar 15]. Available from: https://www.ncbi.nlm.nih.gov/pubmed/17054173 .

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