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372 related items for PubMed ID: 17503046

  • 1. Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method.
    Sura T, Trachoo O, Viprakasit V, Vathesatogkit P, Tunteeratum A, Busabaratana M, Wisedpanichkij R, Isarangkura P.
    Ann Hematol; 2007 Sep; 86(9):659-63. PubMed ID: 17503046
    [Abstract] [Full Text] [Related]

  • 2. Clinical phenotypes and molecular characterization of Hb H-Paksé disease.
    Viprakasit V, Tanphaichitr VS, Pung-Amritt P, Petrarat S, Suwantol L, Fisher C, Higgs DR.
    Haematologica; 2002 Feb; 87(2):117-25. PubMed ID: 11836160
    [Abstract] [Full Text] [Related]

  • 3. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.
    Viprakasit V, Tanphaichitr VS, Veerakul G, Chinchang W, Petrarat S, Pung-Amritt P, Higgs DR.
    Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697
    [Abstract] [Full Text] [Related]

  • 4. Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] with α(0)-thalassemia: molecular and hematological features and differential diagnosis.
    Singha K, Srivorakun H, Fucharoen G, Changtrakul Y, Komwilaisak P, Jetsrisuparb A, Puangplruk R, Fucharoen S.
    Hemoglobin; 2013 Mar; 37(1):37-47. PubMed ID: 23215800
    [Abstract] [Full Text] [Related]

  • 5. 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 Mar; 30(3):349-54. PubMed ID: 16840225
    [Abstract] [Full Text] [Related]

  • 6. Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients.
    Changtrakun Y, Fucharoen S, Ayukarn K, Siriratmanawong N, Fucharoen G, Sanchaisuriya K.
    Ann Hematol; 2002 Jul; 81(7):389-93. PubMed ID: 12185510
    [Abstract] [Full Text] [Related]

  • 7. Novel interactions of two α-Hb variants with SEA deletion α0-thalassemia: hematological and molecular analyses.
    Srivorakun H, Singha K, Fucharoen G, Fucharoen S.
    Hematology; 2018 Apr; 23(3):187-191. PubMed ID: 28945175
    [Abstract] [Full Text] [Related]

  • 8. Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy.
    Siriratmanawong N, Chansri W, Singsanan S, Fucharoen G, Fucharoen S.
    Hemoglobin; 2009 Apr; 33(6):507-14. PubMed ID: 19958198
    [Abstract] [Full Text] [Related]

  • 9. Molecular and clinical features of Hb H disease in northern Thailand.
    Charoenkwan P, Taweephon R, Sae-Tung R, Thanarattanakorn P, Sanguansermsri T.
    Hemoglobin; 2005 Apr; 29(2):133-40. PubMed ID: 15921165
    [Abstract] [Full Text] [Related]

  • 10. Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand.
    Chunpanich S, Ayukarn K, Sanchaisuriya K, Fucharoen G, Fucharoen S.
    Clin Lab Haematol; 2004 Oct; 26(5):355-8. PubMed ID: 15485467
    [Abstract] [Full Text] [Related]

  • 11. 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 Oct; 22(4):264-8. PubMed ID: 17369692
    [Abstract] [Full Text] [Related]

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  • 13. 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 Oct; 32(5):454-61. PubMed ID: 18932070
    [Abstract] [Full Text] [Related]

  • 14. Molecular and hematologic features of hemoglobin E heterozygotes with different forms of alpha-thalassemia in Thailand.
    Sanchaisuriya K, Fucharoen G, Sae-ung N, Jetsrisuparb A, Fucharoen S.
    Ann Hematol; 2003 Oct; 82(10):612-6. PubMed ID: 12955472
    [Abstract] [Full Text] [Related]

  • 15. Diversity in clinical presentation of hemoglobin H disease induced by the SEA deletion and the hemoglobin Quong Sze.
    Liao C, Li J, Xie XM, Zhou JY, Li DZ.
    Ann Hematol; 2009 Nov; 88(11):1145-7. PubMed ID: 19259674
    [No Abstract] [Full Text] [Related]

  • 16. [Analysis of the non-deletion alpha-thalassemia mutations by PCR temperature gradient gel electrophoresis].
    Zhao Y, Xu X, Yang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):51-5. PubMed ID: 11172644
    [Abstract] [Full Text] [Related]

  • 17. Thalassemia intermedia associated with complex interaction of Hb Beijing [alpha16(A14)Lys-->Asn] and Hb E [beta26(B8)Glu-->Lys] with a deletional alpha-thalassemia-1 in a Thai family.
    Fucharoen S, Chunpanich S, Sanchaisuriya K, Fucharoen G, Kunyanone N.
    Hemoglobin; 2005 Feb; 29(1):77-83. PubMed ID: 15768559
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