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169 related items for PubMed ID: 1690325

  • 1. 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 17; 335(8690):637-40. PubMed ID: 1690325
    [Abstract] [Full Text] [Related]

  • 2. The interaction of alpha-thalassemia and homozygous sickle-cell disease.
    Higgs DR, Aldridge BE, Lamb J, Clegg JB, Weatherall DJ, Hayes RJ, Grandison Y, Lowrie Y, Mason KP, Serjeant BE, Serjeant GR.
    N Engl J Med; 1982 Jun 17; 306(24):1441-6. PubMed ID: 6176865
    [Abstract] [Full Text] [Related]

  • 3. Sickle cell disease in Orissa State, India.
    Kar BC, Satapathy RK, Kulozik AE, Kulozik M, Sirr S, Serjeant BE, Serjeant GR.
    Lancet; 1986 Nov 22; 2(8517):1198-201. PubMed ID: 2430154
    [Abstract] [Full Text] [Related]

  • 4. 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 22; 61(7):684-91. PubMed ID: 23620965
    [Abstract] [Full Text] [Related]

  • 5. 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 22; 41(1):83-93. PubMed ID: 420738
    [Abstract] [Full Text] [Related]

  • 6. 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 22; 69(1):89-92. PubMed ID: 2454649
    [Abstract] [Full Text] [Related]

  • 7. Sickle cell-beta +-thalassaemia: a haematological and clinical study in Liberia.
    Bienzle U, Kappes R, Reimer A, Feldheim M, Tischendorf FW, Kohne E.
    Blut; 1983 Nov 22; 47(5):279-85. PubMed ID: 6194836
    [Abstract] [Full Text] [Related]

  • 8. 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 22; 70(4):449-54. PubMed ID: 3219294
    [Abstract] [Full Text] [Related]

  • 9. Concurrent sickle-cell anemia and alpha-thalassemia: effect on severity of anemia.
    Embury SH, Dozy AM, Miller J, Davis JR, Kleman KM, Preisler H, Vichinsky E, Lande WN, Lubin BH, Kan YW, Mentzer WC.
    N Engl J Med; 1982 Feb 04; 306(5):270-4. PubMed ID: 6172710
    [Abstract] [Full Text] [Related]

  • 10. The effect of Hb F and alpha-thalassemia on the red cell indices in sickle cell anemia.
    Milner PF, Garbutt GJ, Nolan-Davis LV, Jonah F, Wilson LB, Wilson JT.
    Am J Hematol; 1986 Apr 04; 21(4):383-95. PubMed ID: 2420172
    [Abstract] [Full Text] [Related]

  • 11. The haematology of steady state homozygous sickle cell disease: interrelationships between haematological indices.
    Maude GH, Hayes RJ, Serjeant GR.
    Br J Haematol; 1987 Aug 04; 66(4):549-58. PubMed ID: 2444245
    [Abstract] [Full Text] [Related]

  • 12. 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 04; 67(2):411-4. PubMed ID: 2417644
    [Abstract] [Full Text] [Related]

  • 13. Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from Georgia.
    Felice AE, McKie KM, Cleek MP, Marino EM, Kutlar A, McKie VC.
    Am J Hematol; 1987 Aug 04; 25(4):389-400. PubMed ID: 2441597
    [Abstract] [Full Text] [Related]

  • 14. 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 04; 77(3):386-91. PubMed ID: 2012764
    [Abstract] [Full Text] [Related]

  • 15. The determinants of irreversibly sickled cells in homozygous sickle cell disease.
    Serjeant GR, Serjeant BE, Desai P, Mason KP, Sewell A, England JM.
    Br J Haematol; 1978 Nov 04; 40(3):431-8. PubMed ID: 749928
    [Abstract] [Full Text] [Related]

  • 16. Two different forms of homozygous sickle cell disease occur in Saudi Arabia.
    Padmos MA, Roberts GT, Sackey K, Kulozik A, Bail S, Morris JS, Serjeant BE, Serjeant GR.
    Br J Haematol; 1991 Sep 04; 79(1):93-8. PubMed ID: 1716963
    [Abstract] [Full Text] [Related]

  • 17. 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 04; 60(2):279-92. PubMed ID: 4005180
    [Abstract] [Full Text] [Related]

  • 18. Clinical manifestation and laboratory findings of sickle cell anaemia in association with alpha-thalassaemia in Saudi Arabia.
    el-Hazmi MA.
    Acta Haematol; 1985 Jun 04; 74(3):155-60. PubMed ID: 2420134
    [Abstract] [Full Text] [Related]

  • 19. 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 04; 148(8):796-804. PubMed ID: 7519102
    [Abstract] [Full Text] [Related]

  • 20. 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 Aug 04; 13(3):229-37. PubMed ID: 1794225
    [Abstract] [Full Text] [Related]

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