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269 related items for PubMed ID: 3629709

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Current observations on sickle cell genotype in Nigeria.
    Nduka N, Owhochuku SM, Odike P.
    East Afr Med J; 1993 Oct; 70(10):646-9. PubMed ID: 7514527
    [Abstract] [Full Text] [Related]

  • 3. Study of haemoglobin S percentage and haematological parameters in sickle cell trait.
    Pathak K, Kishore S, Anshu, Shivkumar VB, Gangane N, Sharma S.
    Indian J Pathol Microbiol; 2003 Jul; 46(3):420-4. PubMed ID: 15025289
    [Abstract] [Full Text] [Related]

  • 4. Biochemical diagnosis in sickle cell disease.
    Isaacs WA.
    Ghana Med J; 1971 Mar; 10(1):40-3. PubMed ID: 5173734
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Hematological findings in 375 Sicilians with Hb S trait.
    Schilirò G, Comisi FF, Testa R, Dibenedetto SP, Samperi P, Marino S.
    Haematologica; 1990 Dec; 75(2):113-6. PubMed ID: 2358201
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. The influence of alpha-thalassaemia on the haematological & clinical expression of sickle cell disease in western India.
    Mukherjee MB, Surve R, Tamankar A, Gangakhedkar RR, Ghosh K, Lu CY, Krishnamoorthy R, Colah R, Mohanty D.
    Indian J Med Res; 1998 Apr; 107():178-81. PubMed ID: 9604545
    [Abstract] [Full Text] [Related]

  • 9. Prevalence of thalassaemias in ethnic Saudi Arabians.
    Ganeshaguru K, Acquaye JK, Samuel AP, Hassounah F, Agyeiobese S, Azrai LM, Sejeny SA, Omer A.
    Trop Geogr Med; 1987 Jul; 39(3):238-43. PubMed ID: 3433339
    [Abstract] [Full Text] [Related]

  • 10. Sickle cell-beta 0-thalassaemia in Saudi Arabia.
    el-Hazmi MA, Al-Swailem AR.
    Hum Hered; 1987 Jul; 37(4):211-6. PubMed ID: 2443440
    [Abstract] [Full Text] [Related]

  • 11. Effect of alpha thalassaemia, G-6-PD deficiency and Hb F on the nature of sickle cell anaemia in south-western Saudi Arabia.
    el-Hazmi MA, al-Swailem AR, Bahakim HM, al-Faleh FZ, Warsy AS.
    Trop Geogr Med; 1990 Jul; 42(3):241-7. PubMed ID: 1705730
    [Abstract] [Full Text] [Related]

  • 12. 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. PubMed ID: 16167711
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Red cell distribution width in sickle cell disease.
    Webster P, Castro O.
    Ann Clin Lab Sci; 1986 Mar; 16(4):274-7. PubMed ID: 3740796
    [Abstract] [Full Text] [Related]

  • 15. On the nature of sickle cell disease in the south-western province of Saudi Arabia.
    el-Hazmi MA, Warsy AS.
    Acta Haematol; 1986 Mar; 76(4):212-6. PubMed ID: 2437751
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. [S hemoglobinopathies in Argentina].
    Abreu MS, Peñalver JA.
    Medicina (B Aires); 1992 Mar; 52(4):341-6. PubMed ID: 1340883
    [Abstract] [Full Text] [Related]

  • 18. Hemoglobin H disease in the eastern region of Saudi Arabia.
    Qadri MI, Islam SA.
    Saudi Med J; 2000 Jul; 21(7):666-71. PubMed ID: 11500731
    [Abstract] [Full Text] [Related]

  • 19. Prevalence of beta-thalassaemia and sickle cell traits in premarital screening in Al-Qassim, Saudi Arabia.
    El-Tayeb EN, Yaqoob M, Abdur-Rahim K, Gustavson KH.
    Genet Couns; 2008 Jul; 19(2):211-8. PubMed ID: 18618996
    [Abstract] [Full Text] [Related]

  • 20. Chromatographic measurements of hemoglobin A2 in blood samples that contain sickle hemoglobin.
    Shokrani M, Terrell F, Turner EA, Aguinaga MD.
    Ann Clin Lab Sci; 2000 Apr; 30(2):191-4. PubMed ID: 10807164
    [Abstract] [Full Text] [Related]

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