Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Editorial
. 2015 Jun;109(6):355-6.
doi: 10.1093/trstmh/trv035.

Sickle-cell disease: a call to action

Affiliations
Editorial

Sickle-cell disease: a call to action

Frédéric B Piel et al. Trans R Soc Trop Med Hyg. 2015 Jun.
No abstract available

Keywords: Genetic disorder; Haemoglobinopathies; Health burden; Sickle-cell anaemia; World Sickle Cell Day.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Weatherall DJ. The inherited diseases of hemoglobin are an emerging global health burden. Blood 2010;115:4331–6. doi:10.1182/blood-2010-01-251348. - DOI - PMC - PubMed
    1. Rees DC, Williams TN, Gladwin MT. Sickle-cell disease. Lancet 2010;376:2018–31. doi:10.1016/s0140-6736(10)61029-x. - DOI - PubMed
    1. Steinberg MH. Predicting clinical severity in sickle cell anaemia. Br J Haematol 2005;129:465–81. doi:10.1111/j.1365-2141.2005.05411.x. - DOI - PubMed
    1. Allison AC. Protection afforded by sickle-cell trait against subtertian malareal infection. Br Med J 1954;1:290–4. - PMC - PubMed
    1. Williams TN, Weatherall DJ. World distribution, population genetics, and health burden of the hemoglobinopathies. Cold Spring Harb Perspect Med 2012;2:a011692 doi:10.1101/cshperspect.a011692. - DOI - PMC - PubMed

Publication types

MeSH terms