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Comment
. 2017 Jul 20;377(3):302-303.
doi: 10.1056/NEJMc1706325.

Sickle Cell Disease

Baba Inusa  1 , Joyce Popoola  2 , Ambroise Wonkam  3
Affiliations
Comment

Sickle Cell Disease

Baba Inusa et al. N Engl J Med. .
No abstract available

PubMed Disclaimer

Comment in

  • Sickle Cell Disease.
    Piel FB, Steinberg MH, Rees DC. Piel FB, et al. N Engl J Med. 2017 Jul 20;377(3):305. doi: 10.1056/NEJMc1706325. N Engl J Med. 2017. PMID: 28723338 No abstract available.

Comment on

  • Sickle Cell Disease.
    Piel FB, Steinberg MH, Rees DC. Piel FB, et al. N Engl J Med. 2017 Apr 20;376(16):1561-1573. doi: 10.1056/NEJMra1510865. N Engl J Med. 2017. PMID: 28423290 Review. No abstract available.

References

    1. Piel FB, Steinberg MH, Rees DC. Sickle cell disease. N Engl J Med 2017;376:1561–73. - PubMed
    1. Molineaux L, Fleming AF, Cornille-Brøgger R, Kagan I, Storey J. Abnormal haemoglobins in the Sudan savanna of Nigeria. III. Malaria, immunoglobulins and antimalarial antibodies in sickle cell disease. Ann Trop Med Parasitol 1979;73:301–10. - PubMed
    1. Inusa BP, Daniel Y, Lawson JO, et al. Sickle cell disease screening in northern Nigeria: the coexistence of B-thalassemia inheritance. Pediat Therapeut 2015;5:262.
    1. Sundell K, Jagannathan P, Huang L, et al. Variable piperaquine exposure significantly impacts protective efficacy of monthly dihydroartemisinin-piperaquine for the prevention of malaria in Ugandan children. Malar J 2015;14:368. - PMC - PubMed
    1. Geard A, Pule GD, Chetcha Chemegni B, et al. Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon. Br J Haematol 2017. May 3 (Epub ahead of print). - PMC - PubMed