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PUBMED FOR HANDHELDS

Journal Abstract Search


287 related items for PubMed ID: 7255798

  • 21. Hemoglobin CHarlem (Georgetown) trait in British Columbia.
    Jollymore BD, Gray GR, Naiman SC.
    CMAJ; 1990 Mar 15; 142(6):599-600. PubMed ID: 2311036
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  • 23. Sickle-cell disease. Two cases in a Romanian family.
    Predescu C, Bratu V, Rădulescu E, Ferche G, Drăgulănescu M.
    Med Interne; 1977 Mar 15; 15(1):67-71. PubMed ID: 841254
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  • 25. 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 15; 9(6):366-74. PubMed ID: 8587004
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  • 26. Mitral valve reconstruction in a compound heterozygote for sickle cell anemia and hemoglobin Lepore.
    Tziomalos K, Garipidou V, Houmpouridou E, Pitsis AA, Basayannis E.
    J Thorac Cardiovasc Surg; 2005 Sep 15; 130(3):932-3. PubMed ID: 16153972
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  • 28. Plasma, erythrocyte and urinary selenium levels in sickle cell homozygotes and traits.
    Kilinç Y.
    Turk J Pediatr; 1993 Sep 15; 35(2):105-9. PubMed ID: 8249189
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  • 29. Hematology problem. Sickle cell anemia.
    Schmidt R.
    Am J Med Technol; 1983 Dec 15; 49(12):871-2. PubMed ID: 6670666
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  • 30. Disease progression in HIV-1-infected patients heterozygous for the sickle hemoglobin gene.
    Sellier P, Masson E, Zini JM, Simoneau G, Magnier JD, Evans J, Bergmann JF.
    AIDS; 2009 Nov 13; 23(17):2362-4. PubMed ID: 19773632
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  • 34. Double heterozygous hemoglobinopathies--diagnostic importance of parent studies.
    Patra SB, Giri DD, Patel RZ, Modi UJ, Amin NS.
    Indian Pediatr; 1983 Jul 13; 20(7):485-8. PubMed ID: 6654480
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  • 35. Sickle cell disease caused by Hb S/Québec-CHORI: treatment with hydroxyurea and response.
    Tubman VN, Bennett CM, Luo HY, Chui DH, Heeney MM.
    Pediatr Blood Cancer; 2007 Aug 13; 49(2):207-10. PubMed ID: 17551985
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  • 36. "Minor" hemoglobinopathies: a risk factor for asthma.
    Palma-Carlos AG, Palma-Carlos ML, Costa AC.
    Eur Ann Allergy Clin Immunol; 2005 May 13; 37(5):177-82. PubMed ID: 15984316
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  • 38. Genetic haemoglobin abnormalities in about 9000 Black and 7000 White newborns; haemoglobin F Dickinson (Agamma97His-Arg), a new variant.
    Schneider RG, Haggard ME, Gustavson LP, Brimhall B, Jones RT.
    Br J Haematol; 1974 Dec 13; 28(4):515-24. PubMed ID: 4455303
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  • 40. Microchromatofocusing of hemoglobins. Increased hemoglobin A2 percentage in sickle cell trait.
    Francina A, Dorléac E, Baudonnet C, Jaccoud P, Delaunay J.
    Clin Chim Acta; 1982 May 20; 121(2):261-4. PubMed ID: 7094341
    [No Abstract] [Full Text] [Related]


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