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Journal Abstract Search

151 related items for PubMed ID: 6547933

  • 1. Life-threatening complications in a child with hemoglobin SD-Los Angeles disease.
    Kelleher JF, Park JO, Kim HC, Schroeder WA.
    Hemoglobin; 1984; 8(3):203-13. PubMed ID: 6547933
    [Abstract] [Full Text] [Related]

  • 2. Does elevated hemoglobin F modulate the phenotype in Hb SD-Los Angeles?
    Adekile A, Mullah-Ali A, Akar NA.
    Acta Haematol; 2010; 123(3):135-9. PubMed ID: 20110664
    [Abstract] [Full Text] [Related]

  • 3. Pneumococcal septicemia and meningitis in an infant with Hb S/D-Los Angeles disease: a failure of neonatal hemoglobinopathy screening.
    Abhyankar SH, Miller ST, Rao SP, Brown AB, Pass KA.
    Hemoglobin; 1991; 15(1-2):119-23. PubMed ID: 1717404
    [No Abstract] [Full Text] [Related]

  • 4. Liquid chromatography used in diagnosis of a rare hemoglobin combination: hemoglobin S/LeporeBoston.
    Wessels RA, Rogers BB, Ou CN, Alcorn R, Buffone GJ.
    Clin Chem; 1986 May; 32(5):903-6. PubMed ID: 3698295
    [Abstract] [Full Text] [Related]

  • 5. Experiences with sickle hemoglobin testing in the Texas Newborn Screening Program.
    Therrell BL, Simmank JL, Wilborn M.
    Pediatrics; 1989 May; 83(5 Pt 2):864-7. PubMed ID: 2717316
    [No Abstract] [Full Text] [Related]

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  • 7. Hb D-Los Angeles in Brazil: simple heterozygotes and associations with beta-thalassemia and with Hb S.
    Zago MA, Costa FF.
    Hemoglobin; 1988 May; 12(4):399-403. PubMed ID: 3170242
    [No Abstract] [Full Text] [Related]

  • 8. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
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  • 9. Hemoglobin S/O(Arab): thirteen new cases and review of the literature.
    Zimmerman SA, O'Branski EE, Rosse WF, Ware RE.
    Am J Hematol; 1999 Apr; 60(4):279-84. PubMed ID: 10203101
    [Abstract] [Full Text] [Related]

  • 10. Phenotypic Diversity of Sickle Cell Disease in Patients with a Double Heterozygosity for Hb S and Hb D-Punjab.
    Torres LS, Okumura JV, Belini-Júnior É, Oliveira RG, Nascimento PP, Silva DG, Lobo CL, Oliani SM, Bonini-Domingos CR.
    Hemoglobin; 2016 Sep; 40(5):356-358. PubMed ID: 27535451
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  • 14. [Stanleyville II, a variant of the abnormal alpha-chain hemoglobin frequent in the north of Zaire. Apropos of a case of sickle cell anemia with S and Stanleyville II/S hemoglobins].
    Van Ros G.
    Ann Soc Belg Med Trop; 1974 Sep; 54(6):483-501. PubMed ID: 4469969
    [No Abstract] [Full Text] [Related]

  • 15. Hb S/Hb Lepore with mild sickling symptoms: a hemoglobin variant with mostly delta-chain sequences ameliorates sickle-cell disease.
    Fairbanks VF, McCormick DJ, Kubik KS, Rezuke WN, Black D, Ochaney MS, Schwartz D.
    Am J Hematol; 1997 Feb; 54(2):164-5. PubMed ID: 9034293
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  • 17. Transfusion medicine illustrated. Hemoglobin D after a red-cell exchange for sickle-cell disease.
    Brecher ME, Park YA, Whinna HC, McClannan LS, Afenyi-Annan A.
    Transfusion; 2008 Nov; 48(11):2277-8. PubMed ID: 19054375
    [No Abstract] [Full Text] [Related]

  • 18. Hemoglobin sickle-lepore: an unusual case of sickle cell disease.
    Romana M, Diara JP, Merghoub T, Kéclard L, Saint-Martin C, Berchel C, Mérault G.
    Acta Haematol; 1997 Nov; 98(3):170-1. PubMed ID: 9352751
    [No Abstract] [Full Text] [Related]

  • 19. The frequency of heterozygosity for S and C hemoglobins in Western Pennsylvania.
    Boggs DR.
    Blood; 1974 Nov; 44(5):699-705. PubMed ID: 4420498
    [No Abstract] [Full Text] [Related]

  • 20. Hemoglobin D Los Angeles in two Caucasian families: hemoglobin SD disease and hemoglobin D thalassemia.
    Schneider RG, Ueda S, Alperin JB, Levin WC, Jones RT, Brimhall B.
    Blood; 1968 Aug; 32(2):250-9. PubMed ID: 5672850
    [No Abstract] [Full Text] [Related]

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