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Items: 1 to 50 of 347

1.

β-Thalassemia Mutations in Jamaica: Geographic Variation in Small Communities.

Serjeant GR, Serjeant BE, Mason KP, Happich M, Kulozik AE.

Hemoglobin. 2018 Sep - Nov;42(5-6):294-296. doi: 10.1080/03630269.2018.1540354. Epub 2019 Jan 9.

PMID:
30626236
2.

Causes of death and early life determinants of survival in homozygous sickle cell disease: The Jamaican cohort study from birth.

Serjeant GR, Chin N, Asnani MR, Serjeant BE, Mason KP, Hambleton IR, Knight-Madden JM.

PLoS One. 2018 Mar 1;13(3):e0192710. doi: 10.1371/journal.pone.0192710. eCollection 2018.

3.

A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal Hemoglobin.

Serjeant GR, Serjeant BE, Hambleton IR, Oakley M, Thein SL, Clark B.

Hemoglobin. 2017 May;41(3):216-217. doi: 10.1080/03630269.2017.1360336. Epub 2017 Sep 5.

PMID:
28870138
4.

The Bone Pain Crisis of Sickle Cell Disease and Malaria: Observations from Gujarat, India.

Patel J, Patel B, Serjeant GR.

Indian J Community Med. 2017 Jul-Sep;42(3):167-169. doi: 10.4103/ijcm.IJCM_334_16.

5.

Variability of homozygous sickle cell disease: The role of alpha and beta globin chain variation and other factors.

Serjeant GR, Vichinsky E.

Blood Cells Mol Dis. 2018 May;70:66-77. doi: 10.1016/j.bcmd.2017.06.004. Epub 2017 Jun 21. Review.

PMID:
28689691
6.

Voluntary premarital screening to prevent sickle cell disease in Jamaica: does it work?

Serjeant GR, Serjeant BE, Mason KP, Gibson F, Gardner R, Warren L, Jonker M.

J Community Genet. 2017 Apr;8(2):133-139. doi: 10.1007/s12687-017-0294-8. Epub 2017 Mar 1.

7.

Newborn screening for sickle cell disease in Jamaica: logistics and experience with umbilical cord samples.

Serjeant GR, Serjeant BE, Mason KP, Gardner R, Warren L, Gibson F, Coombs M.

J Community Genet. 2017 Jan;8(1):17-22. doi: 10.1007/s12687-016-0283-3. Epub 2016 Oct 29.

8.

Evolving locally appropriate models of care for indian sickle cell disease.

Serjeant GR.

Indian J Med Res. 2016 Apr;143(4):405-13. doi: 10.4103/0971-5916.184282. Review.

9.

Pregnancy in sickle cell-haemoglobin C (SC) disease. A retrospective study of birth size and maternal weight gain.

Thame MM, Singh-Minott I, Osmond C, Melbourne-Chambers RH, Serjeant GR.

Eur J Obstet Gynecol Reprod Biol. 2016 Aug;203:16-9. doi: 10.1016/j.ejogrb.2016.05.002. Epub 2016 May 16.

10.

Sickle cell disease in India: A perspective.

Serjeant GR, Ghosh K, Patel J.

Indian J Med Res. 2016 Jan;143(1):21-4. doi: 10.4103/0971-5916.178582. No abstract available.

11.

Newborn Screening for Sickle Cell Disease: Jamaican Experience.

Mason K, Gibson F, Gardner R, Warren L, Fisher C, Higgs D, Happich M, Kulozik A, Hambleton I, Serjeant BE, Serjeant GR.

West Indian Med J. 2015 Sep 22;65(1):18-26. doi: 10.7727/wimj.2015.492.

PMID:
26901597
12.

Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica.

Mason K, Gibson F, Gardner RA, Serjeant B, Serjeant GR.

J Community Genet. 2016 Apr;7(2):127-32. doi: 10.1007/s12687-015-0258-9. Epub 2015 Dec 2.

13.

The Chhattisgarh state screening programme for the sickle cell gene: a cost-effective approach to a public health problem.

Patra PK, Khodiar PK, Hambleton IR, Serjeant GR.

J Community Genet. 2015 Oct;6(4):361-8. doi: 10.1007/s12687-015-0222-8. Epub 2015 Mar 31.

14.

Newborn screening for sickle cell disease in India: the need for defining optimal clinical care.

Patel J, Serjeant GR.

Indian J Pediatr. 2014 Mar;81(3):229-30. doi: 10.1007/s12098-013-1218-1. Epub 2013 Sep 14. No abstract available.

PMID:
24037477
15.

The natural history of sickle cell disease.

Serjeant GR.

Cold Spring Harb Perspect Med. 2013 Oct 1;3(10):a011783. doi: 10.1101/cshperspect.a011783. Review.

16.

Fetal growth in women with homozygous sickle cell disease: an observational study.

Thame MM, Osmond C, Serjeant GR.

Eur J Obstet Gynecol Reprod Biol. 2013 Sep;170(1):62-6. doi: 10.1016/j.ejogrb.2013.04.013. Epub 2013 Jun 6.

PMID:
23746798
17.

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
18.

Jamaica, the Caribbean and sickle cell disease.

Serjeant GR.

West Indian Med J. 2012 Jul;61(4):331-7.

PMID:
23240465
19.

Screening for the sickle cell gene in Gujarat, India: a village-based model.

Patel J, Patel B, Gamit N, Serjeant GR.

J Community Genet. 2013 Jan;4(1):43-7. doi: 10.1007/s12687-012-0116-y. Epub 2012 Sep 29.

20.

Elevated IL-1α and CXCL10 serum levels occur in patients with homozygous sickle cell disease and a history of acute splenic sequestration.

Driss A, Wilson NO, Mason K, Hyacinth HI, Hibbert JM, Serjeant GR, Stiles JK.

Dis Markers. 2012;32(5):295-300. doi: 10.3233/DMA-2011-0888.

21.

Counselling mothers of babies with the sickle cell trait: to be or not to be.

Serjeant GR, Serjeant BE.

West Indian Med J. 2011 Jun;60(3):249-50. No abstract available.

PMID:
22224333
22.

Screening for the sickle cell gene in Chhattisgarh state, India: an approach to a major public health problem.

Patra PK, Chauhan VS, Khodiar PK, Dalla AR, Serjeant GR.

J Community Genet. 2011 Sep;2(3):147-51. doi: 10.1007/s12687-011-0050-4. Epub 2011 Jun 15.

23.

Perinatal factors in students admitted to the University of the West Indies data from the Jamaican Perinatal Study.

Foster-Williams K, Younger N, Brown-Dennis A, Ashley DE, McCaw-Binns A, Samms-Vaughan M, Williams W, Serjeant GR.

West Indian Med J. 2010 Jun;59(3):295-9.

PMID:
21291110
24.

Hb S-β-thalassemia: molecular, hematological and clinical comparisons.

Serjeant GR, Serjeant BE, Fraser RA, Hambleton IR, Higgs DR, Kulozik AE, Donaldson A.

Hemoglobin. 2011;35(1):1-12. doi: 10.3109/03630269.2010.546306.

PMID:
21250876
25.

One hundred years of sickle cell disease.

Serjeant GR.

Br J Haematol. 2010 Dec;151(5):425-9. doi: 10.1111/j.1365-2141.2010.08419.x. Epub 2010 Oct 19.

PMID:
20955412
26.

Retained placenta in homozygous sickle cell disease.

Simms-Stewart D, Thame M, Hemans-Keen A, Hambleton I, Serjeant GR.

Obstet Gynecol. 2009 Oct;114(4):825-8. doi: 10.1097/AOG.0b013e3181b6f762.

PMID:
19888041
27.

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
28.

Inhaled nitric oxide for acute chest syndrome in people with sickle cell disease.

Al Hajeri A, Serjeant GR, Fedorowicz Z.

Cochrane Database Syst Rev. 2008 Jan 23;(1):CD006957. doi: 10.1002/14651858.CD006957. Review.

PMID:
18254121
29.

Growth curves for normal Jamaican neonates.

Samms-Vaughan M, Thame M, Osmond C, Hambleton IR, McCaw-Binns A, Ashley DE, Serjeant GR.

West Indian Med J. 2006 Dec;55(6):368-74.

PMID:
17691230
30.

Albuminuria and renal function in homozygous sickle cell disease: observations from a cohort study.

Thompson J, Reid M, Hambleton I, Serjeant GR.

Arch Intern Med. 2007 Apr 9;167(7):701-8.

PMID:
17420429
31.

Elderly survivors with homozygous sickle cell disease.

Serjeant GR, Higgs DR, Hambleton IR.

N Engl J Med. 2007 Feb 8;356(6):642-3. No abstract available.

PMID:
17287491
32.

Bacteraemia in homozygous sickle cell disease in Africa: is pneumococcal prophylaxis justified?

Kizito ME, Mworozi E, Ndugwa C, Serjeant GR.

Arch Dis Child. 2007 Jan;92(1):21-3. Epub 2006 Mar 10.

33.

Phenotype/genotype relationships in sickle cell disease: a pilot twin study.

Weatherall MW, Higgs DR, Weiss H, Weatherall DJ, Serjeant GR.

Clin Lab Haematol. 2005 Dec;27(6):384-90.

PMID:
16307540
34.

Leg ulceration in sickle cell disease: medieval medicine in a modern world.

Serjeant GR, Serjeant BE, Mohan JS, Clare A.

Hematol Oncol Clin North Am. 2005 Oct;19(5):943-56, viii-ix. Review.

PMID:
16214654
35.

Incidence and natural history of proliferative sickle cell retinopathy: observations from a cohort study.

Downes SM, Hambleton IR, Chuang EL, Lois N, Serjeant GR, Bird AC.

Ophthalmology. 2005 Nov;112(11):1869-75. Epub 2005 Sep 19.

PMID:
16171867
36.

Sickle cell disease in Uganda: a time for action.

Serjeant GR, Ndugwa CM.

East Afr Med J. 2003 Jul;80(7):384-7. Review.

PMID:
16167756
37.

Sickle haemoglobin and haemoglobin Stanleyville II: possible confusion with sickle cell-haemoglobin C disease.

Serjeant GR, Wild B, Tebasulwa S, Mason KP, Serjeant BE, Ndugwa CM.

East Afr Med J. 2005 Jul;82(7):367-70.

PMID:
16167711
38.
39.

Mortality from sickle cell disease in Africa.

Serjeant GR.

BMJ. 2005 Feb 26;330(7489):432-3. No abstract available.

40.

The dilemma of defining clinical severity in homozygous sickle cell disease.

Serjeant GR.

Curr Hematol Rep. 2004 Sep;3(5):307-9. Review. No abstract available.

PMID:
15341695
41.

Sickle cell disease in Saudi Arabia: the Asian haplotype. Reflections on a meeting at Hofuf, September 2003.

Serjeant GR, Serjeant BE.

Ann Saudi Med. 2004 May-Jun;24(3):166-8. No abstract available.

42.

Are there clinical phenotypes of homozygous sickle cell disease?

Alexander N, Higgs D, Dover G, Serjeant GR.

Br J Haematol. 2004 Aug;126(4):606-11.

PMID:
15287956
43.

Outcome of pregnancy in homozygous sickle cell disease.

Serjeant GR, Loy LL, Crowther M, Hambleton IR, Thame M.

Obstet Gynecol. 2004 Jun;103(6):1278-85.

PMID:
15172865
44.

Chronic leg ulceration in homozygous sickle cell disease: the role of venous incompetence.

Clare A, FitzHenley M, Harris J, Hambleton I, Serjeant GR.

Br J Haematol. 2002 Nov;119(2):567-71.

PMID:
12406102
45.

Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease.

Taylor JG 6th, Tang DC, Savage SA, Leitman SF, Heller SI, Serjeant GR, Rodgers GP, Chanock SJ.

Blood. 2002 Dec 15;100(13):4303-9. Epub 2002 Aug 15.

PMID:
12393616
46.

Patterns of low-affinity immunoglobulin receptor polymorphisms in stroke and homozygous sickle cell disease.

Taylor JG, Tang D, Foster CB, Serjeant GR, Rodgers GP, Chanock SJ.

Am J Hematol. 2002 Feb;69(2):109-14.

47.

Haematological response to parvovirus B19 infection in homozygous sickle-cell disease.

Serjeant BE, Hambleton IR, Kerr S, Kilty CG, Serjeant GR.

Lancet. 2001 Nov 24;358(9295):1779-80.

PMID:
11734237
48.

Foetal haemoglobin in homozygous sickle cell disease: a study of patients with low HBF levels.

Donaldson A, Thomas P, Serjeant BE, Serjeant GR.

Clin Lab Haematol. 2001 Oct;23(5):285-9.

PMID:
11703409
49.

Mass spectral analysis of asymmetric hemoglobin hybrids: demonstration of Hb FS (alpha2gammabetaS) in sickle cell disease.

Ofori-Acquah SF, Green BN, Davies SC, Nicolaides KH, Serjeant GR, Layton DM.

Anal Biochem. 2001 Nov 1;298(1):76-82.

PMID:
11673898
50.

Sickle cell disease and age at menarche in Jamaican girls: observations from a cohort study.

Serjeant GR, Singhal A, Hambleton IR.

Arch Dis Child. 2001 Nov;85(5):375-8.

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