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PUBMED FOR HANDHELDS

Journal Abstract Search


158 related items for PubMed ID: 23221516

  • 1. Hemoglobin SO-Arab and α-thalassemia diagnosed in an adult: A case-based review of the hemoglobinopathies.
    Zacharia G, Maronge GF, Brazda FW, Boulmay BC.
    Am J Med Sci; 2013 Oct; 346(4):325-7. PubMed ID: 23221516
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Screening of military recruits for hemoglobin variants.
    Uddin DE, Dickson LG, Brodine CE.
    JAMA; 1974 Mar 25; 227(12):1405-7. PubMed ID: 4406024
    [No Abstract] [Full Text] [Related]

  • 4. 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 25; 60(4):279-84. PubMed ID: 10203101
    [Abstract] [Full Text] [Related]

  • 5. The role of a sickle cell center in comprehensive screening and counseling for sickle cell and related disorders.
    Lutcher CL, Huisman TH, Dorsey WM, Mayson S, Ludvigsen B, Smith AT.
    South Med J; 1974 Mar 25; 67(3):259-64. PubMed ID: 4814171
    [No Abstract] [Full Text] [Related]

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  • 7. Frequency of sickling disorders in U.S. blacks.
    Motulsky AG.
    N Engl J Med; 1973 Jan 04; 288(1):31-3. PubMed ID: 4681897
    [No Abstract] [Full Text] [Related]

  • 8.
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  • 9. 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 04; 30(2):191-4. PubMed ID: 10807164
    [Abstract] [Full Text] [Related]

  • 10. Screening for sickle cell hemoglobinopathy and thalassemia.
    Motulsky AG.
    Isr J Med Sci; 1973 Apr 04; 9(9):1341-9. PubMed ID: 4775114
    [No Abstract] [Full Text] [Related]

  • 11. Laboratory recognition of a rare hemoglobinopathy: hemoglobins SS and SG(Philadelphia) associated with alpha-thalassemia-2.
    Kirk CM, Papadea CN, Lazarchick J.
    Arch Pathol Lab Med; 1999 Oct 04; 123(10):963-6. PubMed ID: 10506456
    [Abstract] [Full Text] [Related]

  • 12. The frequency of heterozygosity for S and C hemoglobins in Western Pennsylvania.
    Boggs DR.
    Blood; 1974 Nov 04; 44(5):699-705. PubMed ID: 4420498
    [No Abstract] [Full Text] [Related]

  • 13. [Diagnosis of thalassemias and hemoglobinopathies by HPLC (high performance liquid chromatography): study of 627 patients].
    Sabo G, Brodbeck U, Cardile N, Viollier AF, Scheurmann T, Knecht H.
    Schweiz Med Wochenschr; 1999 Aug 28; 129(34):1196-200. PubMed ID: 10486859
    [Abstract] [Full Text] [Related]

  • 14. Hemoglobin S/Hemoglobin Quebec-Chori Presenting as Sickle Cell Disease: A Case Report.
    Goode E, Boruchov D, Oliveira JL, Lau CC.
    J Pediatr Hematol Oncol; 2020 Nov 28; 42(8):e775-e777. PubMed ID: 32657857
    [Abstract] [Full Text] [Related]

  • 15. Validation of an automated HPLC method for quantification of hemoglobin S.
    Fisher SI, Haga JA, Castleberry SM, Hall RB, Thompson WC.
    Clin Chem; 1997 Sep 28; 43(9):1667-9. PubMed ID: 9299955
    [No Abstract] [Full Text] [Related]

  • 16. A rapid test for sickle hemoglobin.
    Asakura T, Segal ME, Friedman S, Schwartz E.
    JAMA; 1975 Jul 14; 233(2):156-6. PubMed ID: 1173442
    [Abstract] [Full Text] [Related]

  • 17. Editorial: The background to sickling.
    Br J Ophthalmol; 1974 Jul 14; 58(7):641-3. PubMed ID: 4423125
    [No Abstract] [Full Text] [Related]

  • 18. Automated mass screening for hemoglobin S: a rational method.
    Nalbandian RM, Camp FR, Conte NF, Prothro WB.
    Health Serv Rep; 1973 Feb 14; 88(2):165-73. PubMed ID: 4769325
    [No Abstract] [Full Text] [Related]

  • 19. Life-threatening complications in a child with hemoglobin SD-Los Angeles disease.
    Kelleher JF, Park JO, Kim HC, Schroeder WA.
    Hemoglobin; 1984 Feb 14; 8(3):203-13. PubMed ID: 6547933
    [Abstract] [Full Text] [Related]

  • 20. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct 14; 64(4):1024-32. PubMed ID: 479366
    [Abstract] [Full Text] [Related]


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