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Journal Abstract Search

270 related items for PubMed ID: 15025289

  • 1.
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  • 2. The haematological, biochemical and clinical--presentation of haemoglobin S in Saudi Arabia (i). Haematological & clinical expression.
    El-Hazmi MA, Jabbar FA, Al-Faleh FZ, Al-Swailem AR, Warsy AS.
    Trop Geogr Med; 1987 Apr; 39(2):157-62. PubMed ID: 3629709
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  • 4. Haematological study in sickle cell homozygous and heterozygous children in the age group 0-6 years.
    Walke VA, Walde MS.
    Indian J Pathol Microbiol; 2007 Oct; 50(4):901-4. PubMed ID: 18306601
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  • 5. Haemoglobin-S in sickle cell trait with papillary necrosis.
    Ahmed SG, Ibrahim UA.
    Br J Haematol; 2006 Nov; 135(3):415-6. PubMed ID: 16984389
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  • 6. Detection of alpha thalassaemia in sickle cell trait patients by Hb-Bart's screening & quantitation of Hb-A & Hb-S.
    Misra RC.
    Indian J Med Res; 1989 Dec; 90():459-62. PubMed ID: 2628314
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  • 8. Comparative haematological parameters of HbAA and HbAS genotype children infected with Plasmodium falciparum malaria in Yemen.
    Albiti AH, Nsiah K.
    Hematology; 2014 Apr; 19(3):169-74. PubMed ID: 24074341
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  • 9. Red blood cell counts and indices in sickle cell trait in a black American population.
    Castro O, Scott RB.
    Hemoglobin; 1985 Apr; 9(1):65-7. PubMed ID: 3997542
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  • 11. The effect of hemolysis on plasma oxidation and nitration in patients with sickle cell disease.
    Kupesiz A, Celmeli G, Dogan S, Antmen B, Aslan M.
    Free Radic Res; 2012 Jul; 46(7):883-90. PubMed ID: 22509726
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  • 12. The distribution of haemoglobin S and other haemoglobin variants in a sample of Liberian paediatric subjects.
    Simbeye AG.
    Biochem Exp Biol; 1978 Jul; 14(4):335-8. PubMed ID: 757517
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  • 15. [Red cell system and selected red cell enzymes in men occupationally exposed to mercury vapours].
    Zabiński Z, Rutowski J, Moszczyński P, Dabrowski Z.
    Przegl Lek; 2006 Jul; 63 Suppl 7():74-83. PubMed ID: 17784549
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  • 16. Correlation of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency and sickle cell trait (Hb-AS).
    Nhonoli AM, Kujwalile JM, Kigoni EP, Masawe AE.
    Trop Geogr Med; 1978 Mar; 30(1):99-101. PubMed ID: 675833
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  • 17. Optimal haematocrit in subjects with normal haemoglobin genotype (HbAA), sickle cell trait (HbAS), and homozygous sickle cell disease (HbSS).
    Bowers AS, Pepple DJ, Reid HL.
    Clin Hemorheol Microcirc; 2011 Mar; 47(4):253-60. PubMed ID: 21654054
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  • 18. Fibrinolytic activity in adult Kenyan patients with sickle cell disease.
    Aluoch JR.
    East Afr Med J; 1998 Jun; 75(6):351-2. PubMed ID: 9803619
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  • 19. Mean cell haemoglobin concentration in subjects with haemoglobin C, D, E and S traits.
    Hinchliffe RF, Norcliffe D, Farrar LM, Lilleyman JS.
    Clin Lab Haematol; 1996 Dec; 18(4):245-8. PubMed ID: 9054696
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  • 20. Red cell distribution width in sickle cell disease.
    Webster P, Castro O.
    Ann Clin Lab Sci; 1986 Dec; 16(4):274-7. PubMed ID: 3740796
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