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Journal Abstract Search

451 related items for PubMed ID: 8587004

  • 1. Utilization of monoclonal-antibody-based assay (HemoCard in screening for and differentiating between genotypes of sickle cell disease and other hemoglobinopathies.
    Schultz JC.
    J Clin Lab Anal; 1995; 9(6):366-74. PubMed ID: 8587004
    [Abstract] [Full Text] [Related]

  • 2. [Clinical and hematological profile of Lepore Hemoglobin in Ivory Coast].
    Sangare A, Sanogo I, Meite M, Segbena A, Toure AH, Elenga JP, Siransy L, Allangba O.
    Med Trop (Mars); 1994; 54(1):43-6. PubMed ID: 8196525
    [Abstract] [Full Text] [Related]

  • 3. Identification of hemoglobins and hemoglobinopathies by electrophoresis on cellulose acetate plates impregnated with citrate agar.
    Schneider RG, Hosty TS, Tomlin G, Atkins R.
    Clin Chem; 1974; 20(1):74-7. PubMed ID: 4809474
    [No Abstract] [Full Text] [Related]

  • 4. Comparison of Sebia Capillarys capillary electrophoresis with the Primus high-pressure liquid chromatography in the evaluation of hemoglobinopathies.
    Keren DF, Hedstrom D, Gulbranson R, Ou CN, Bak R.
    Am J Clin Pathol; 2008 Nov; 130(5):824-31. PubMed ID: 18854277
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  • 6. A rare case of a compound heterozygote hemoglobin S/hemoglobin Fannin-Lubbock-I individual. Is it a sickling disorder?
    Burns NK, Risin SA.
    Lab Hematol; 2010 Jun; 16(2):26-7. PubMed ID: 20534428
    [No Abstract] [Full Text] [Related]

  • 7. Sickle-cell anemia and other hemoglobinopathies. Procedures and strategy for screening employing spots of blood on filter paper as specimens.
    Garrick MD, Dembure P, Guthrie R.
    N Engl J Med; 1973 Jun 14; 288(24):1265-8. PubMed ID: 4703315
    [No Abstract] [Full Text] [Related]

  • 8. Preventation of thalassemia in Australia.
    Hendy J.
    Southeast Asian J Trop Med Public Health; 1999 Jun 14; 30 Suppl 2():94-6. PubMed ID: 11400797
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  • 13. Experiences with sickle hemoglobin testing in the Texas Newborn Screening Program.
    Therrell BL, Simmank JL, Wilborn M.
    Pediatrics; 1989 May 14; 83(5 Pt 2):864-7. PubMed ID: 2717316
    [No Abstract] [Full Text] [Related]

  • 14. A comprehensive screening program for hemoglobinopathies.
    Barnes MG, Komarmy L, Novack AH.
    JAMA; 1972 Feb 14; 219(6):701-5. PubMed ID: 5066694
    [No Abstract] [Full Text] [Related]

  • 15. Quantitative analysis of abnormal hemoglobins by agar gel electrophoresis.
    Steiman I, Norwood C, Charache S.
    J Lab Clin Med; 1985 Mar 14; 105(3):328-30. PubMed ID: 3973468
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  • 17. Hemoglobin G-Philadelphia-S. A family study of an inherited hybrid hemoglobin.
    Rising JA, Sautter RL, Spicer SJ.
    Am J Clin Pathol; 1974 Jan 14; 61(1):92-102. PubMed ID: 4809151
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  • 18. Accuracy of cord blood screening for sickle hemoglobinopathies. Three- to five-year follow-up.
    Kramer MS, Rooks Y, Johnston D, Pearson HA.
    JAMA; 1979 Feb 02; 241(5):485-6. PubMed ID: 759662
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  • 19. Voxelotor Treatment Interferes With Quantitative and Qualitative Hemoglobin Variant Analysis in Multiple Sickle Cell Disease Genotypes.
    Rutherford-Parker NJ, Campbell ST, Colby JM, Shajani-Yi Z.
    Am J Clin Pathol; 2020 Oct 13; 154(5):627-634. PubMed ID: 32561909
    [Abstract] [Full Text] [Related]

  • 20. Hemoglobin O arab in four negro families and its interaction with hemoglobin S and hemoglobin C.
    Milner PF, Miller C, Grey R, Seakins M, DeJong WW, Went LN.
    N Engl J Med; 1970 Dec 24; 283(26):1417-25. PubMed ID: 5481775
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