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Items: 1 to 20 of 22


Awareness of Sickle Cell Trait Status: A Cross-Sectional Survey of Antenatal Women in Ghana.

Obed SA, Asah-Opoku K, Aboagye S, Torto M, Oppong SA, Nuamah MA.

Am J Trop Med Hyg. 2017 Mar;96(3):735-740. doi: 10.4269/ajtmh.16-0396. Epub 2017 Apr 6.


An Expert Review of Pharmacogenomics of Sickle Cell Disease Therapeutics: Not Yet Ready for Global Precision Medicine.

Mnika K, Pule GD, Dandara C, Wonkam A.

OMICS. 2016 Oct;20(10):565-574. Epub 2016 Sep 16.


Comparative Analysis of Iron Homeostasis in Sub-Saharan African Children with Sickle Cell Disease and Their Unaffected Siblings.

Gomez S, Diawara A, Gbeha E, Awadalla P, Sanni A, Idaghdour Y, Rahimy MC.

Front Pediatr. 2016 Feb 23;4:8. doi: 10.3389/fped.2016.00008. eCollection 2016.


Complications of sickle cell anaemia in children in Northwestern Tanzania.

Saidi H, Smart LR, Kamugisha E, Ambrose EE, Soka D, Peck RN, Makani J.

Hematology. 2016 May;21(4):248-56. doi: 10.1080/10245332.2015.1101976. Epub 2016 Feb 17.


Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients.

Wonkam A, Makani J, Ofori-Aquah S, Nnodu OE, Treadwell M, Royal C, Ohene-Frempong K; Members of the H3Africa Consortium..

Cardiovasc J Afr. 2015 Mar-Apr;26(2 Suppl 1):S50-5. doi: 10.5830/CVJA-2015-040. Review.


Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State.

Akodu SO, Njokanma OF, AdeoluKehinde O.

Int J Hematol Oncol Stem Cell Res. 2015 Jan 1;9(1):5-9.


Health policy for sickle cell disease in Africa: experience from Tanzania on interventions to reduce under-five mortality.

Makani J, Soka D, Rwezaula S, Krag M, Mghamba J, Ramaiya K, Cox SE, Grosse SD.

Trop Med Int Health. 2015 Feb;20(2):184-7. doi: 10.1111/tmi.12428. Epub 2014 Nov 17.


Sickle cell disease: new opportunities and challenges in Africa.

Makani J, Ofori-Acquah SF, Nnodu O, Wonkam A, Ohene-Frempong K.

ScientificWorldJournal. 2013;2013:193252. doi: 10.1155/2013/193252. Epub 2013 Sep 19. Review.


Pilot study of hemoglobinopathies in newborns of the Rafael Calvo maternity clinic of Cartagena, Colombia.

Alvear CC, Barboza M, Viola M, Moneriz C, Araque LM.

Colomb Med (Cali). 2012 Sep 30;43(3):196-9. eCollection 2012 Jul.


Genomic architecture of sickle cell disease in West African children.

Quinlan J, Idaghdour Y, Goulet JP, Gbeha E, de Malliard T, Bruat V, Grenier JC, Gomez S, Sanni A, Rahimy MC, Awadalla P.

Front Genet. 2014 Feb 14;5:26. doi: 10.3389/fgene.2014.00026. eCollection 2014.


Association of care in a medical home and health care utilization among children with sickle cell disease.

Raphael JL, Rattler TL, Kowalkowski MA, Brousseau DC, Mueller BU, Giordano TP.

J Natl Med Assoc. 2013 Summer;105(2):157-65.


Evidence review of hydroxyurea for the prevention of sickle cell complications in low-income countries.

Mulaku M, Opiyo N, Karumbi J, Kitonyi G, Thoithi G, English M.

Arch Dis Child. 2013 Nov;98(11):908-14. doi: 10.1136/archdischild-2012-302387. Epub 2013 Aug 30. Review.


Routine paediatric sickle cell disease (SCD) outpatient care in a rural Kenyan hospital: utilization and costs.

Amendah DD, Mukamah G, Komba A, Ndila C, Williams TN.

PLoS One. 2013 Apr 9;8(4):e61130. doi: 10.1371/journal.pone.0061130. Print 2013.


Mortality rates and age at death from sickle cell disease: U.S., 1979-2005.

Lanzkron S, Carroll CP, Haywood C Jr.

Public Health Rep. 2013 Mar-Apr;128(2):110-6.


Pediatric hospital medicine and children with medical complexity: past, present, and future.

Simon TD, Mahant S, Cohen E.

Curr Probl Pediatr Adolesc Health Care. 2012 May;42(5):113-9. doi: 10.1016/j.cppeds.2012.01.002. Review.


Renal status of children with sickle cell disease in Accra, Ghana.

Osei-Yeboah CT, Rodrigues O.

Ghana Med J. 2011 Dec;45(4):155-60.


Hospital-based comprehensive care programs for children with special health care needs: a systematic review.

Cohen E, Jovcevska V, Kuo DZ, Mahant S.

Arch Pediatr Adolesc Med. 2011 Jun;165(6):554-61. doi: 10.1001/archpediatrics.2011.74. Review.


Children with medical complexity: an emerging population for clinical and research initiatives.

Cohen E, Kuo DZ, Agrawal R, Berry JG, Bhagat SK, Simon TD, Srivastava R.

Pediatrics. 2011 Mar;127(3):529-38. doi: 10.1542/peds.2010-0910. Epub 2011 Feb 21. Review.


An up-date on the prevalence of sickle cell trait in Eastern and Western Uganda.

Okwi AL, Byarugaba W, Ndugwa CM, Parkes A, Ocaido M, Tumwine JK.

BMC Blood Disord. 2010 Jun 23;10:5. doi: 10.1186/1471-2326-10-5.

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