239 related articles for article (PubMed ID: 4005180)
1. Haematological change in sickle cell-haemoglobin C disease and in sickle cell-beta thalassaemia: a cohort study from birth.
Stevens MC; Maude GH; Beckford M; Grandison Y; Mason K; Serjeant BE; Taylor B; Topley JM; Serjeant GR
Br J Haematol; 1985 Jun; 60(2):279-92. PubMed ID: 4005180
[TBL] [Abstract][Full Text] [Related]
2. The red cell distribution width in sickle cell disease--is it of clinical value?
Thame M; Grandison Y; Mason K; Thompson M; Higgs D; Morris J; Serjeant B; Serjeant G
Clin Lab Haematol; 1991; 13(3):229-37. PubMed ID: 1794225
[TBL] [Abstract][Full Text] [Related]
3. The development of haematological changes in homozygous sickle cell disease: a cohort study from birth to 6 years.
Serjeant GR; Grandison Y; Lowrie Y; Mason K; Phillips J; Serjeant BE; Vaidya S
Br J Haematol; 1981 Aug; 48(4):533-43. PubMed ID: 7272216
[TBL] [Abstract][Full Text] [Related]
4. A comparison of sickle cell syndromes in northern Greece.
Christakis J; Vavatsi N; Hassapopoulou H; Angeloudi M; Papadopoulou M; Loukopoulos D; Morris JS; Serjeant BE; Serjeant GR
Br J Haematol; 1991 Mar; 77(3):386-91. PubMed ID: 2012764
[TBL] [Abstract][Full Text] [Related]
5. Sickle cell-hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromes.
Murray N; Serjeant BE; Serjeant GR
Br J Haematol; 1988 May; 69(1):89-92. PubMed ID: 2454649
[TBL] [Abstract][Full Text] [Related]
6. Subclassification of HbS syndrome: is it necessary?
Tyagi S; Choudhry VP; Saxena R
Clin Lab Haematol; 2003 Dec; 25(6):377-81. PubMed ID: 14641142
[TBL] [Abstract][Full Text] [Related]
7. The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia.
Vyas P; Higgs DR; Weatherall DJ; Dunn D; Serjeant BE; Serjeant GR
Br J Haematol; 1988 Dec; 70(4):449-54. PubMed ID: 3219294
[TBL] [Abstract][Full Text] [Related]
8. Comparison of sickle cell-beta0 thalassaemia with homozygous sickle cell disease.
Serjeant GR; Sommereux AM; Stevenson M; Mason K; Serjeant BE
Br J Haematol; 1979 Jan; 41(1):83-93. PubMed ID: 420738
[TBL] [Abstract][Full Text] [Related]
9. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
Adeyemo T; Ojewunmi O; Oyetunji A
Pan Afr Med J; 2014; 18():71. PubMed ID: 25400838
[TBL] [Abstract][Full Text] [Related]
10. Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative Study of Sickle Cell Disease.
Brown AK; Sleeper LA; Miller ST; Pegelow CH; Gill FM; Waclawiw MA
Arch Pediatr Adolesc Med; 1994 Aug; 148(8):796-804. PubMed ID: 7519102
[TBL] [Abstract][Full Text] [Related]
11. Alpha thalassaemia and the haematology of normal Jamaican children.
Maude GH; Higgs DR; Beckford M; Grandison Y; Mason K; Taylor B; Serjeant BE; Serjeant GR
Clin Lab Haematol; 1985; 7(4):289-95. PubMed ID: 2420505
[TBL] [Abstract][Full Text] [Related]
12. Effect of alpha thalassaemia on the rheology of homozygous sickle cell disease.
Serjeant BE; Mason KP; Kenny MW; Stuart J; Higgs DR; Weatherall DJ; Hayes RJ; Serjeant GR
Br J Haematol; 1983 Nov; 55(3):479-86. PubMed ID: 6639889
[TBL] [Abstract][Full Text] [Related]
13. The development of haemoglobin A2 in normal negro infants and in sickle cell disease.
Serjeant BE; Mason KP; Serjeant GR
Br J Haematol; 1978 Jun; 39(2):259-65. PubMed ID: 678477
[TBL] [Abstract][Full Text] [Related]
14. Comparison of homozygous sickle cell disease in northern Greece and Jamaica.
Christakis J; Vavatsi N; Hassapopoulou H; Papadopoulou M; Mandraveli K; Loukopoulos D; Morris JS; Serjeant BE; Serjeant GR
Lancet; 1990 Mar; 335(8690):637-40. PubMed ID: 1690325
[TBL] [Abstract][Full Text] [Related]
15. Haematological characteristics of the beta 0 thalassaemia trait in Sardinian children.
Galanello R; De Virgiliis S; Addis M; Paglietti E; Ruggeri R; Cao A
J Clin Pathol; 1980 Oct; 33(10):946-8. PubMed ID: 7430359
[TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 11668096
[TBL] [Abstract][Full Text] [Related]
17. Blood film features of sickle cell-haemoglobin C disease.
Bain BJ
Br J Haematol; 1993 Mar; 83(3):516-8. PubMed ID: 8485058
[TBL] [Abstract][Full Text] [Related]
18. The haematology of steady state homozygous sickle cell disease: interrelationships between haematological indices.
Maude GH; Hayes RJ; Serjeant GR
Br J Haematol; 1987 Aug; 66(4):549-58. PubMed ID: 2444245
[TBL] [Abstract][Full Text] [Related]
19. Comparison of haematological features of the beta0 and beta+ thalassaemia traits in Jamaican Negroes.
Millard DP; Mason K; Serjeant BE; Serjeant GR
Br J Haematol; 1977 Jun; 36(2):161-70. PubMed ID: 871430
[TBL] [Abstract][Full Text] [Related]
20. Alpha thalassemia and the hematology of homozygous sickle cell disease in childhood.
Stevens MC; Maude GH; Beckford M; Grandison Y; Mason K; Taylor B; Serjeant BE; Higgs DR; Teal H; Weatherall DJ
Blood; 1986 Feb; 67(2):411-4. PubMed ID: 2417644
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]