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B E Serjeant

Explore the profile of B E Serjeant including associated specialties, affiliations and a list of published articles. Areas
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Articles 81
Citations 975
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Recent Articles
1.
Serjeant G, Serjeant B, Mason K, Gibson F, Gardner R, Warren L, et al.
J Community Genet . 2023 Jun; 14(4):355-360. PMID: 37391652
The objective of this study was to review the prevalence and features of the beta thalassaemia trait in Jamaican populations. Screening of 221,306 newborns over the last 46 years has...
2.
Serjeant G, Serjeant B, Mason K, Gibson F, Osmond C, Thein S, et al.
J Community Genet . 2022 Jan; 13(2):229-234. PMID: 35018573
Based in the parish of Manchester in central Jamaica, the Manchester Project offered free detection of haemoglobin genotype to senior classes in 15 secondary schools between 2008 and 2013. Restricting...
3.
Serjeant G, Serjeant B, Mason K, Gibson F, Gardner R, Warren L, et al.
J Community Genet . 2017 Mar; 8(2):133-139. PMID: 28251585
To determine whether identifying haemoglobin genotype, and providing education and counselling to senior school students will influence their choice of partner and reduce the frequency of births with sickle cell...
4.
Serjeant G, Serjeant B, Mason K, Gardner R, Warren L, Gibson F, et al.
J Community Genet . 2016 Nov; 8(1):17-22. PMID: 27796853
The study aims to describe the logistics and results of a programme for newborn screening for sickle cell disease based on samples from the umbilical cord. Samples were dried on...
5.
Mason K, Gibson F, Gardner R, Warren L, Fisher C, Higgs D, et al.
West Indian Med J . 2016 Feb; 65(1):18-26. PMID: 26901597
Objectives: To review the history of newborn screening for sickle cell disease with especial reference to Jamaica. Methods: A summary was done of the history, the development of associated laboratory...
6.
Ndugwa C, Higgs D, Fisher C, Hambleton I, Mason K, Serjeant B, et al.
West Indian Med J . 2013 Apr; 61(7):684-91. PMID: 23620965
Objective: To compare the haematological and clinical features of homozygous sickle cell (SS) disease in Bantu and Benin haplotypes in a cross-sectional study of 115 Ugandan patients attending the Sickle...
7.
Serjeant G, Serjeant B
West Indian Med J . 2012 Jan; 60(3):249-50. PMID: 22224333
No abstract available.
8.
Serjeant G, Serjeant B, Mason K, Hambleton I, Fisher C, Higgs D
Int J Lab Hematol . 2008 Jul; 31(6):585-96. PMID: 18644042
Earlier reports on homozygous sickle cell (SS) disease have been biased by severely affected cases. The Jamaican clinic which seeks to avoid such bias has 102 patients surviving beyond 60...
9.
Serjeant G, Wild B, Tebasulwa S, Mason K, Serjeant B, Ndugwa C
East Afr Med J . 2005 Sep; 82(7):367-70. PMID: 16167711
Objectives: To bring to the attention of East African practitioners, the characteristics of Hb Stanleyville II, its interaction with HbS, and the resemblance of the double heterozygote to sickle cell-haemoglobin...
10.
Serjeant B, Hambleton I, Kerr S, Kilty C, Serjeant G
Lancet . 2001 Dec; 358(9295):1779-80. PMID: 11734237
Infection with human parvovirus B19 is known to cause aplastic crises in patients with homozygous sickle-cell disease. We studied the haematological consequences of parvovirus B19 infection in 280 such patients...