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Journal Abstract Search

160 related items for PubMed ID: 15768554

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  • 2. Hb Constant Spring [alpha 142, Term-->Gln (TAA>CAA in alpha2)] in the alpha-thalassemia of anemic patients in Myanmar.
    Ne-Win, Harano K, Harano T, Kyaw-Shwe, Aye-Aye-Myint, Khin-Thander-Aye, Okada S.
    Hemoglobin; 2008; 32(5):454-61. PubMed ID: 18932070
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  • 3. alpha-thalassemia mutations in Khuzestan Province, Southwest Iran.
    Zandian K, Nateghi J, Keikhaie B, Pedram M, Hafezi-Nejad N, Hadavi V, Oberkanins C, Azarkeivan A, Law HY, Najmabadi H.
    Hemoglobin; 2008; 32(6):546-52. PubMed ID: 19065332
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  • 6. Molecular and clinical features of Hb H disease in northern Thailand.
    Charoenkwan P, Taweephon R, Sae-Tung R, Thanarattanakorn P, Sanguansermsri T.
    Hemoglobin; 2005; 29(2):133-40. PubMed ID: 15921165
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  • 7. Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects.
    Fucharoen S, Fucharoen G.
    Hemoglobin; 2012; 36(1):18-24. PubMed ID: 22145566
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  • 8. Hb H (beta4) disease in Cukurova, Southern Turkey.
    Cürük MA.
    Hemoglobin; 2007; 31(2):265-71. PubMed ID: 17486510
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  • 9. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N, Pinmuang-Ngam C, Fucharoen G, Fucharoen S.
    Fetal Diagn Ther; 2007; 22(4):264-8. PubMed ID: 17369692
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  • 15. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
    Harteveld CL, Versteegh FG, Kok PJ, van Rooijen-Nijdam IH, van Delft P, Giordano PC.
    Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225
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  • 17. Identification of α-globin chain variants: a report from Iran.
    Akbari MT, Hamid M.
    Arch Iran Med; 2012 Sep; 15(9):564-7. PubMed ID: 22924376
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  • 19. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.
    Li D, Liao C, Li J, Xie X, Huang Y, Zhong H.
    Haematologica; 2006 May; 91(5):649-51. PubMed ID: 16627247
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  • 20. Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion.
    Harteveld CL, Versteegh FG, van Leer EH, Starreveld JS, Kok PJ, van Rooijen-Nijdam I, van Delft P, Zanella-Cleon I, Becchi M, Wajcman H, Giordano PC.
    Hemoglobin; 2007 May; 31(3):313-23. PubMed ID: 17654068
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