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Journal Abstract Search

646 related items for PubMed ID: 16987801

  • 1. The prevalence and molecular basis of hemoglobinopathies in Cambodia.
    Carnley BP, Prior JF, Gilbert A, Lim E, Devenish R, Sing H, Sarin E, Guhadasan R, Sullivan SG, Wise CA, Bittles AH, Chan K, Wong MS, Chan V, Erber WN.
    Hemoglobin; 2006; 30(4):463-70. PubMed ID: 16987801
    [Abstract] [Full Text] [Related]

  • 2. 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; 33(6):507-14. PubMed ID: 19958198
    [Abstract] [Full Text] [Related]

  • 3. 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; 36(1):47-56. PubMed ID: 22122810
    [Abstract] [Full Text] [Related]

  • 4. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
    Efremov GD.
    Hemoglobin; 2007; 31(1):1-15. PubMed ID: 17365000
    [Abstract] [Full Text] [Related]

  • 5. 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; 37(2):176-82. PubMed ID: 23234508
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 7. Molecular Epidemiology of Hemoglobinopathies in Cambodia.
    Munkongdee T, Tanakulmas J, Butthep P, Winichagoon P, Main B, Yiannakis M, George J, Devenish R, Fucharoen S, Svasti S.
    Hemoglobin; 2016 Jun; 40(3):163-7. PubMed ID: 27117566
    [Abstract] [Full Text] [Related]

  • 8. Misdiagnosis of Hb constant spring (alpha142, Term-->Gln, TAA-->CAA in alpha2) in a Hb H (beta4) disease child.
    Li D, Liao C, Li J.
    Hemoglobin; 2007 Jun; 31(1):105-8. PubMed ID: 17365012
    [Abstract] [Full Text] [Related]

  • 9. Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families.
    Fucharoen S, Sanchaisuriya K, Fucharoen G, Panyasai S, Devenish R, Luy L.
    Haematologica; 2003 Oct; 88(10):1092-8. PubMed ID: 14555303
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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 Oct; 29(1):77-83. PubMed ID: 15768559
    [Abstract] [Full Text] [Related]

  • 12. Inherited hemoglobin disorders in Guinea-Bissau, West Africa: a population study.
    Masmas TN, Garly ML, Lisse IM, Rodriques A, Petersen PT, Birgens H.
    Hemoglobin; 2006 Oct; 30(3):355-64. PubMed ID: 16840226
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Detection of Hb Constant Spring [α142, Term→Gln, TAA>CAA (α2)] in heterozygotes combined with β-thalassemia.
    Li YQ, Li R, Li DZ.
    Hemoglobin; 2013 Feb; 37(2):197-200. PubMed ID: 23390935
    [Abstract] [Full Text] [Related]

  • 15. 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 Feb; 36(5):491-6. PubMed ID: 22881835
    [Abstract] [Full Text] [Related]

  • 16. Hemoglobinopathies mimicking Hb S/beta-thalassemia: Hb S/S with alpha-thalassemia and Hb S/Volga.
    Luo HY, Heeney M, Wang WC, Eung SH, Ware RE, Steinberg MH, Chui DH.
    Am J Hematol; 2006 May; 81(5):361-5. PubMed ID: 16628724
    [Abstract] [Full Text] [Related]

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

  • 18. 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]

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  • 20. 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]

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