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Journal Abstract Search

405 related items for PubMed ID: 11475035

  • 1. [Beta-thalassemia: clinical manifestations].
    Perrimond H.
    Bull Soc Pathol Exot; 2001 May; 94(2):92-4. PubMed ID: 11475035
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  • 2. 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; 30(2):191-4. PubMed ID: 10807164
    [Abstract] [Full Text] [Related]

  • 3. Clinical phenotypes and molecular diagnosis in a hitherto interaction of Hb E/beta thalassemia syndrome (beta(E)/beta(-31), (A -->G)).
    Vathana N, Viprakasit V, Sanpakit K, Chinchang W, Veerakul G, Tanphaichitr V.
    J Med Assoc Thai; 2005 Nov; 88 Suppl 8():S66-71. PubMed ID: 16856429
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  • 4. Alpha and beta thalassemia.
    Muncie HL, Campbell J.
    Am Fam Physician; 2009 Aug 15; 80(4):339-44. PubMed ID: 19678601
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  • 5. Erythroid bone marrow activity and red cell hemoglobinization in iron sufficient beta-thalassemia heterozygotes as reflected by soluble transferrin receptor and reticulocyte hemoglobin in content. Correlation with genotypes and Hb A(2) levels.
    Skarmoutsou C, Papassotiriou I, Traeger-Synodinos J, Stamou H, Ladis V, Metaxotou-Mavrommati A, Stamoulakatou A, Kanavakis E.
    Haematologica; 2003 Jun 15; 88(6):631-6. PubMed ID: 12801838
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  • 6. Heart failure in beta-thalassemia syndromes: a decade of progress.
    Hahalis G, Alexopoulos D, Kremastinos DT, Zoumbos NC.
    Am J Med; 2005 Sep 15; 118(9):957-67. PubMed ID: 16164878
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  • 7. Insight onto the pathophysiology and clinical complications of thalassemia intermedia.
    Cappellini MD, Musallam KM, Taher AT.
    Hemoglobin; 2009 Sep 15; 33 Suppl 1():S145-59. PubMed ID: 20001620
    [Abstract] [Full Text] [Related]

  • 8. Molecular basis of asymptomatic beta-thalassemia major in an African American individual.
    Ballas SK, Cai SP, Gabuzda T, Chehab FF.
    Am J Med Genet; 1997 Mar 17; 69(2):196-9. PubMed ID: 9056561
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  • 9. Linear growth in homozygous beta-thalassemia and beta-thalassemia/hemoglobin E patients under different treatment regimens.
    Viprakasit V, Tanphaichitr VS, Mahasandana C, Assteerawatt A, Suwantol L, Veerakul G, Kankirawatana S, Pung-Amritt P, Suvatte V.
    J Med Assoc Thai; 2001 Jul 17; 84(7):929-41. PubMed ID: 11759973
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  • 11. Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia.
    Ma ES, Chan AY, Au WY, Yeung YM, Chan LC.
    Haematologica; 2001 Apr 17; 86(4):432-3. PubMed ID: 11325652
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  • 14. [Beta(o)/beta(o) thalassemia with a mild phenotype].
    Hémar C, Nibourel O, Maboudou P, Méreau-Richard C, Badens C, Rousseaux J, Rose C.
    Ann Biol Clin (Paris); 2006 Apr 17; 64(4):341-5. PubMed ID: 16829478
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  • 15. Thalassemia intermedia: revisited.
    Taher A, Isma'eel H, Cappellini MD.
    Blood Cells Mol Dis; 2006 Apr 17; 37(1):12-20. PubMed ID: 16737833
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  • 18. Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.
    Bibi A, Messaoud T, Fattoum S.
    Hemoglobin; 2006 Apr 17; 30(2):175-81. PubMed ID: 16798642
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