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PUBMED FOR HANDHELDS

Journal Abstract Search


160 related items for PubMed ID: 1173442

  • 1. 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]

  • 2. Standardization in detection of abnormal hemoglobins. Solubility tests for hemoglobin S.
    Schmidt RM, Wilson SM.
    JAMA; 1973 Sep 03; 225(10):1225-30. PubMed ID: 4740985
    [No Abstract] [Full Text] [Related]

  • 3. Screening for abnormal hemoglobins: who, when, and how.
    McCurdy PR.
    Prim Care; 1980 Sep 03; 7(3):451-60. PubMed ID: 6905205
    [Abstract] [Full Text] [Related]

  • 4. Comparison of results for three method of hemoglobin S identification.
    Hicksg EJ, Griep JA, Nordschow CD.
    Clin Chem; 1973 May 03; 19(5):533-5. PubMed ID: 4703665
    [No Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct 25; 64(4):1024-32. PubMed ID: 479366
    [Abstract] [Full Text] [Related]

  • 7. 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 25; 90():459-62. PubMed ID: 2628314
    [Abstract] [Full Text] [Related]

  • 8. 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 25; 54(2):164-5. PubMed ID: 9034293
    [Abstract] [Full Text] [Related]

  • 9. Newborn screening for sickle cell and other hemoglobinopathies: a Canadian pilot study.
    Yorke D, Mitchell J, Clow C, Nuguid E, Cadogan R, Sinclair D, Luscombe S, Rozen R, Meredith P, Esseltine D.
    Clin Invest Med; 1992 Aug 25; 15(4):376-83. PubMed ID: 1516295
    [Abstract] [Full Text] [Related]

  • 10. [Possibility of separating hemoglobin F and hemoglobin S by electrophoresis on cellulose acetate].
    Ingiulla A, D'Asero G.
    Riv Clin Pediatr; 1967 Aug 25; 80(4):151-6. PubMed ID: 5605657
    [No Abstract] [Full Text] [Related]

  • 11. Sickle cell trait.
    McCurdy PR.
    Am Fam Physician; 1974 Nov 25; 10(5):141-6. PubMed ID: 4421745
    [No Abstract] [Full Text] [Related]

  • 12. A new rapid differentiating solubility test for hemoglobin S.
    Warren B, Crosby G, Evans GL.
    Am J Med Technol; 1975 Sep 25; 41(9):317-21. PubMed ID: 1180257
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Detection of unsuspected hemoglobin S by reticulocyte stain.
    Liu PI, McGregor DH, Gates LE, Poindexter AR.
    Am J Med Technol; 1974 Mar 25; 40(3):138-41. PubMed ID: 4131241
    [No Abstract] [Full Text] [Related]

  • 15. 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 Mar 25; 9(6):366-74. PubMed ID: 8587004
    [Abstract] [Full Text] [Related]

  • 16. 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 25; 16(2):26-7. PubMed ID: 20534428
    [No Abstract] [Full Text] [Related]

  • 17. 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 25; 346(4):325-7. PubMed ID: 23221516
    [Abstract] [Full Text] [Related]

  • 18. HB S-HB Monroe; a sickle cell-beta-thalassemia syndrome.
    Sweeting I, Serjeant BE, Serjeant GR, Kulozik AE, Vetter B.
    Hemoglobin; 1998 Mar 25; 22(2):153-6. PubMed ID: 9576332
    [No Abstract] [Full Text] [Related]

  • 19. False-positive Hb S in the Helena Sickle-Thal Quik Column method, owing to the presence of another hemoglobin variant.
    Tegelaers FP, Seelen PJ.
    Clin Chem; 1988 Mar 25; 34(3):601. PubMed ID: 3349621
    [No Abstract] [Full Text] [Related]

  • 20. Evaluation of SICKLEQUIK, a differential solubility test for hemoglobin S.
    Del Guidice RE, Doering KM, Teran A.
    Am J Med Technol; 1979 Apr 25; 45(4):287-9. PubMed ID: 433978
    [Abstract] [Full Text] [Related]


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