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Journal Abstract Search

576 related items for PubMed ID: 15485467

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  • 3. 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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  • 8. 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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  • 9. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy.
    Sanchaisuriya K, Chunpanich S, Fucharoen S, Fucharoen G, Sanchaisuriya P, Changtrakun Y.
    Eur J Haematol; 2005 Mar; 74(3):221-7. PubMed ID: 15693792
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  • 10. 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
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  • 11. 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 Feb; 37(1):37-47. PubMed ID: 23215800
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  • 12. Molecular and haematological characterization of compound Hb E/Hb Pyrgos and Hb E/Hb J-Bangkok in Thai patients.
    Fucharoen S, Singsanan S, Sanchaisuriya K, Fucharoen G.
    Clin Lab Haematol; 2005 Jun; 27(3):184-9. PubMed ID: 15938724
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  • 13. First description of a Hb A2 variant in Thailand. Identification of Hb A2-Melbourne [δ43(CD2)Glu→Lys] in Thai individuals.
    Chaibunruang A, Fucharoen G, Fucharoen S.
    Hemoglobin; 2012 Jun; 36(1):80-4. PubMed ID: 21967556
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  • 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
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  • 15. Hemoglobin Q-Thailand related disorders: origin, molecular, hematological and diagnostic aspects.
    Singsanan S, Karnpean R, Fucharoen G, Sanchaisuriya K, Sae-Ung N, Fucharoen S.
    Blood Cells Mol Dis; 2010 Oct 15; 45(3):210-4. PubMed ID: 20615730
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  • 16. 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 15; 23(3):187-191. PubMed ID: 28945175
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  • 17. Interactions of hemoglobin Lepore (deltabeta hybrid hemoglobin) with various hemoglobinopathies: A molecular and hematological characteristics and differential diagnosis.
    Chaibunruang A, Srivorakun H, Fucharoen S, Fucharoen G, Sae-ung N, Sanchaisuriya K.
    Blood Cells Mol Dis; 2010 Mar 15; 44(3):140-5. PubMed ID: 20022270
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  • 18. 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 Mar 15; 22(4):264-8. PubMed ID: 17369692
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  • 19. Molecular and hematological characterization of hemoglobin Hope/hemoglobin E and hemoglobin Hope/alpha-thalassemia 2 in Thai patients.
    Chunpanich S, Fucharoen S, Sanchaisuriya K, Fucharoen G, Kam-itsara K.
    Lab Hematol; 2004 Mar 15; 10(4):215-20. PubMed ID: 15697092
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  • 20. 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 15; 30(3):349-54. PubMed ID: 16840225
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