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Items: 1 to 20 of 100

1.

Survival estimates for patients with homozygous sickle-cell disease in Jamaica: a clinic-based population study.

Wierenga KJ, Hambleton IR, Lewis NA.

Lancet. 2001 Mar 3;357(9257):680-3.

PMID:
11247552
2.

Gallstones in sickle cell disease: observations from The Jamaican Cohort study.

Walker TM, Hambleton IR, Serjeant GR.

J Pediatr. 2000 Jan;136(1):80-5.

PMID:
10636979
3.

Improved survival in homozygous sickle cell disease: lessons from a cohort study.

Lee A, Thomas P, Cupidore L, Serjeant B, Serjeant G.

BMJ. 1995 Dec 16;311(7020):1600-2.

4.

Mortality in sickle cell disease. Life expectancy and risk factors for early death.

Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, Klug PP.

N Engl J Med. 1994 Jun 9;330(23):1639-44.

5.

Newborn sickle cell disease screening: the Jamaican experience (1995-2006).

King L, Fraser R, Forbes M, Grindley M, Ali S, Reid M.

J Med Screen. 2007;14(3):117-22.

PMID:
17925083
6.

The changing face of homozygous sickle cell disease: 102 patients over 60 years.

Serjeant GR, Serjeant BE, Mason KP, Hambleton IR, Fisher C, Higgs DR.

Int J Lab Hematol. 2009 Dec;31(6):585-96. doi: 10.1111/j.1751-553X.2008.01089.x. Epub 2008 Jul 17.

PMID:
18644042
7.

Clinical findings associated with homozygous sickle cell disease in the Barbadian population--do we need a national SCD registry?

Quimby KR, Moe S, Sealy I, Nicholls C, Hambleton IR, Landis RC.

BMC Res Notes. 2014 Feb 22;7:102. doi: 10.1186/1756-0500-7-102.

8.

Management of sickle cell disease; lessons from the Jamaican Cohort Study.

Serjeant GR, Serjeant BE.

Blood Rev. 1993 Sep;7(3):137-45. Review.

PMID:
8241829
9.

Growth, morbidity, and mortality in a cohort of Jamaican adolescents with homozygous sickle cell disease.

Ashcroft MT, Serijant GR.

West Indian Med J. 1981 Dec;30(4):197-201. No abstract available.

PMID:
7344303
10.
11.

Homozygous sickle cell disease in Uganda and Jamaica a comparison of Bantu and Benin haplotypes.

Ndugwa C, Higgs D, Fisher C, Hambleton I, Mason K, Serjeant BE, Serjeant GR.

West Indian Med J. 2012 Oct;61(7):684-91.

PMID:
23620965
12.

[Homozygous sickle cell disease in patients above 20 years of age: follow-up of 108 patients in Dakar].

Diop S, Mokono SO, Ndiaye M, Touré Fall AO, Thiam D, Diakhaté L.

Rev Med Interne. 2003 Nov;24(11):711-5. French.

PMID:
14604747
14.

Impact of a Comprehensive Sickle Cell Center on Early Childhood Mortality in a Developing Country: The Jamaican Experience.

King LG, Bortolusso-Ali S, Cunningham-Myrie CA, Reid ME.

J Pediatr. 2015 Sep;167(3):702-5.e1. doi: 10.1016/j.jpeds.2015.06.028. Epub 2015 Jul 7.

PMID:
26163082
15.

Subjective well-being of adults with homozygous sickle cell disease in Jamaica.

Thomas JA, Lipps GE.

West Indian Med J. 2011 Mar;60(2):181-7.

PMID:
21942124
16.

Testosterone deficiency and extreme retardation of puberty in homozygous sickle-cell disease.

Singhal A, Gabay L, Serjeant GR.

West Indian Med J. 1995 Mar;44(1):20-3.

PMID:
7793108
17.

Quality of life in patients with sickle cell disease in Jamaica: rural-urban differences.

Asnani MR, Reid ME, Ali SB, Lipps G, Williams-Green P.

Rural Remote Health. 2008 Apr-Jun;8(2):890. Epub 2008 Apr 11.

18.

Sickle cell disease in Britain.

Brozović M, Anionwu E.

J Clin Pathol. 1984 Dec;37(12):1321-6.

19.

Psychological distress and coping in sickle cell disease: comparison of British and Jamaican attitudes.

Thomas VJ, Hambleton I, Serjeant G.

Ethn Health. 2001 May;6(2):129-36.

PMID:
11480961
20.

Early deaths in Jamaican children with sickle cell disease.

Rogers DW, Clarke JM, Cupidore L, Ramlal AM, Sparke BR, Serjeant GR.

Br Med J. 1978 Jun 10;1(6126):1515-6.

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