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Journal Abstract Search


206 related items for PubMed ID: 22881835

  • 1. Unmasking Hb Paksé (codon 142, TAA>TAT, α2) and its combinations in patients also carrying Hb Constant Spring (codon 142, TAA>CAA, α2) in northern Thailand.
    Pornprasert S, Panyasai S, Treesuwan K.
    Hemoglobin; 2012; 36(5):491-6. PubMed ID: 22881835
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  • 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
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  • 3. Detection of coinherited Hb H-Constant Spring/Paksé disease and Hb E by capillary electrophoresis and high performance liquid chromatography.
    Pornprasert S, Waneesorn J.
    Hemoglobin; 2013 Feb; 37(2):176-82. PubMed ID: 23234508
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  • 4. Molecular screening of the Hbs Constant Spring (codon 142, TAA>CAA, α2) and Paksé (codon 142, TAA>TAT, α2) mutations in Thailand.
    Pichanun D, Munkongdee T, Klamchuen S, Butthep P, Winichagoon P, Fucharoen S, Svasti S.
    Hemoglobin; 2010 Feb; 34(6):582-6. PubMed ID: 21077767
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  • 5. Hb Paksé [(alpha2) codon 142 (TAA-->TAT or Term-->Tyr)J in Thai patients with EAbart's disease and Hb H Disease.
    Sanchaisuriya K, Fucharoen G, Fucharoen S.
    Hemoglobin; 2002 Aug; 26(3):227-35. PubMed ID: 12403487
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  • 9. 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 Aug; 32(5):454-61. PubMed ID: 18932070
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  • 11. Association of Hb Shenyang [α26(B7)Ala→Glu, GCG>GAG, HBA2: c.80C>A (or HBA1)] with Several Types of α-Thalassemia in Thailand.
    Panyasai S, Kongthai K, Phasit A.
    Hemoglobin; 2020 Sep; 44(5):354-360. PubMed ID: 33023349
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  • 12. Comparison between capillary electrophoresis and high performance liquid chromatography for detection and quantification of Hb constant spring [Hb CS; α142, Term→Gln (TAA>CAA IN α2)].
    Waneesorn J, Panyasai S, Kongthai K, Singboottra P, Pornprasert S.
    Hemoglobin; 2011 Sep; 35(4):338-45. PubMed ID: 21797701
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  • 13. Hb Koya Dora [alpha142, Term-->Ser (TAA>TCA in alpha2)]: a rare mutation of the alpha2 gene stop codon associated with alpha-thalassemia.
    Brennan SO, Ryken S, Chan T.
    Hemoglobin; 2010 Sep; 34(4):402-5. PubMed ID: 20642339
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  • 15. Presentation of Compound Heterozygous Hemoglobin Constant Spring and Hemoglobin Pakse in Neonates.
    Komvilaisak P, Jetsrisuparb A, Fucharoen G, Komwilaisak R, Jirapradittha J, Kiatchoosakun P.
    J Pediatr Hematol Oncol; 2019 Aug; 41(6):e413-e415. PubMed ID: 30615015
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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. Micromapping of thalassemia and hemoglobinopathies in diferent regions of northeast Thailand and Vientiane, Laos People's Democratic Republic.
    Tritipsombut J, Sanchaisuriya K, Phollarp P, Bouakhasith D, Sanchaisuriya P, Fucharoen G, Fucharoen S, Schelp FP.
    Hemoglobin; 2012 Oct; 36(1):47-56. PubMed ID: 22122810
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