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172 related items for PubMed ID: 9494047

  • 1. Hb Tak confirmed by DNA analysis: not expressed as thalassemia in a Hb Tak/Hb E compound heterozygote.
    Hoyer JD, Wick MJ, Thibodeau SN, Viker KA, Conner R, Fairbanks VF.
    Hemoglobin; 1998 Jan; 22(1):45-52. PubMed ID: 9494047
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  • 2. Compound heterozygous Hb Tak/Hb E causes secondary erythrocytosis in a Thai family.
    Teawtrakul N, Sirijirachai C, Chansung G, Fucharoen G.
    Hemoglobin; 2010 Jan; 34(2):165-8. PubMed ID: 20353353
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  • 3. 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
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  • 4. Interactions of unstable hemoglobin Rush with thalassemia and hemoglobin E result in thalassemia intermedia.
    Huang K, Ge S, Yi W, Bi H, Lin K, Sun H, Huang X, Chu J, Ma S, Yang Z.
    Hematology; 2019 Dec; 24(1):459-466. PubMed ID: 31124399
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  • 5. Complex interaction of Hb Hekinan [alpha27(B8) Glu-Asp] and Hb E [beta26(B8) Glu-Lys] with a deletional alpha-thalassemia 1 in a Thai family.
    Fucharoen S, Changtrakun Y, Ratanasiri T, Fucharoen G, Sanchaisuriya K.
    Eur J Haematol; 2003 May; 70(5):304-9. PubMed ID: 12694166
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  • 6. Hb T-Cambodia, a beta chain variant with the mutations of Hb E and Hb D-Punjab, confirmed by DNA analysis.
    Hutt PJ, Fairbanks VF, Thibodeau SN, Green MM, Hoyer JD, Block SH, Day C, Jones RT, Barwick RC.
    Hemoglobin; 1997 May; 21(3):205-18. PubMed ID: 9140717
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  • 7. Five hemoglobin variants in a double heterozygote for α- and β-globin chain defects.
    Singha K, Fucharoen G, Fucharoen S.
    Acta Haematol; 2014 May; 131(2):71-5. PubMed ID: 24081021
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  • 9. Development of a High Resolution Melting Curve Analysis for the Detection of Hemoglobin δ-Chain Variants in Thailand and Identification of Hb A2-Walsgrave [codon 52 (GAT>CAT), Asp→His; HBD:c.157G>C] in a Pregnant Woman from Southern Thailand.
    Prajantasen T, Prayalaw P, Panyasai S, Binlee S, Nongnuan S.
    Genet Test Mol Biomarkers; 2021 Jun; 25(6):426-433. PubMed ID: 34152843
    [Abstract] [Full Text] [Related]

  • 10. Secondary erythrocytosis caused by hemoglobin Tak/(δβ)0-thalassemia syndrome.
    Prakobkaew N, Singsanan S, Fucharoen G, Surapot S, Fucharoen S.
    Acta Haematol; 2010 Jun; 124(2):115-9. PubMed ID: 20798489
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  • 11. Double heterozigosity HbE/alpha-thalassemia in a Cambodian child.
    Perutelli P, Schenone A, Scuderi F.
    Haematologica; 1986 Jun; 71(1):44-5. PubMed ID: 3084355
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  • 14. Concomitant inheritance of alpha-thalassemia in beta 0- thalassemia/Hb E disease.
    Winichagoon P, Fucharoen S, Weatherall D, Wasi P.
    Am J Hematol; 1985 Nov; 20(3):217-22. PubMed ID: 2998183
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  • 17. 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
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  • 18. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α(+)-thalassemia.
    Srivorakun H, Fucharoen G, Puangplruk R, Kheawon N, Fucharoen S.
    Eur J Haematol; 2011 Jul; 87(1):68-72. PubMed ID: 21447006
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  • 20. 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 Jul; 33(6):507-14. PubMed ID: 19958198
    [Abstract] [Full Text] [Related]

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