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Journal Abstract Search

371 related items for PubMed ID: 503635

  • 1.
    ; . PubMed ID:
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  • 2. Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.
    Honig GR, Gunay U, Mason RG, Vida LN, Ferenc C.
    Pediatr Res; 1976 Jun; 10(6):613-20. PubMed ID: 1272638
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  • 4. The interaction of alpha-thalassemia and homozygous sickle-cell disease.
    Higgs DR, Aldridge BE, Lamb J, Clegg JB, Weatherall DJ, Hayes RJ, Grandison Y, Lowrie Y, Mason KP, Serjeant BE, Serjeant GR.
    N Engl J Med; 1982 Jun 17; 306(24):1441-6. PubMed ID: 6176865
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  • 5. Hemoglobin synthesis studies of a family with alpha-thalassemia trait and sickle cell trait.
    Shaeffer JR, DeSimone J, Kleve LJ.
    Biochem Genet; 1975 Dec 17; 13(11-12):783-8. PubMed ID: 1200978
    [Abstract] [Full Text] [Related]

  • 6. Alpha thalassaemia in adults with sickle-cell trait.
    Steinberg MH, Adams JG, Dreiling BJ.
    Br J Haematol; 1975 May 17; 30(1):31-7. PubMed ID: 1191571
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  • 8. Hemoglobinopathies among five major ethnic groups in Karachi, Pakistan.
    Ghani R, Manji MA, Ahmed N.
    Southeast Asian J Trop Med Public Health; 2002 Dec 17; 33(4):855-61. PubMed ID: 12757239
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  • 10. Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease.
    Noguchi CT, Dover GJ, Rodgers GP, Serjeant GR, Antonarakis SE, Anagnou NP, Higgs DR, Weatherall DJ, Schechter AN.
    J Clin Invest; 1985 May 17; 75(5):1632-7. PubMed ID: 2581999
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  • 11. Concurrent sickle-cell anemia and alpha-thalassemia: effect on severity of anemia.
    Embury SH, Dozy AM, Miller J, Davis JR, Kleman KM, Preisler H, Vichinsky E, Lande WN, Lubin BH, Kan YW, Mentzer WC.
    N Engl J Med; 1982 Feb 04; 306(5):270-4. PubMed ID: 6172710
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  • 12. 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]

  • 13. Haemoglobin C/alpha thalassaemia: haematological and biosynthetic studies.
    Steinberg MH.
    Br J Haematol; 1975 Jul 04; 30(3):337-42. PubMed ID: 1201216
    [Abstract] [Full Text] [Related]

  • 14. [Biological profile of sickle cell anemia in Morocco. A propos of 85 cases].
    Omari M, Naji M, Agoumi N.
    Maghrib Tibbi; 1982 Jul 04; 4(2-3):175-82. PubMed ID: 7182694
    [No Abstract] [Full Text] [Related]

  • 15. The occurrence and identification of alpha-thalassemia-2 among hemoglobin S heterozygotes.
    Felice AE, Altay CA, Milner PF, Huisman TH.
    Am J Clin Pathol; 1981 Jul 04; 76(1):70-3. PubMed ID: 7258153
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  • 17. Clinical and molecular correlations in the sickle/beta+-thalassemia syndrome.
    Atweh GF, Forget BG.
    Am J Hematol; 1987 Jan 04; 24(1):31-6. PubMed ID: 3799593
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  • 18. Alpha-thalassemia in a pool of individuals of Eti-Turk origin with hemoglobin S (Hb S).
    Jama H, Gürgey A, Altay C.
    Turk J Pediatr; 1987 Jan 04; 29(1):1-14. PubMed ID: 3433374
    [No Abstract] [Full Text] [Related]

  • 19. Association of Hb H disease with sickle-trait.
    Martinez G, Ferreira R, Hernandez A, Di Rienzo A, Colombo B.
    Hemoglobin; 1986 Jan 04; 10(4):421-5. PubMed ID: 3744872
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  • 20. Sickle cell traits in Canada. Trimodal distribution of Hb S as a result of interaction with alpha-thalassaemia gene.
    Wong SC, Ali MA, Boyadjian SE.
    Acta Haematol; 1981 Jan 04; 65(3):157-63. PubMed ID: 6165216
    [Abstract] [Full Text] [Related]

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