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91 related items for PubMed ID: 11146568

  • 1. Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA].
    Harteveld CL, Traeger-Synodinos J, Ragusa A, Fichera M, Kanavakis E, Kattamis C, Giordano P, Schilirò G, Bernini LF.
    Haematologica; 2001 Jan; 86(1):36-8. PubMed ID: 11146568
    [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. Molecular characterization and origins of Hb Constant Spring and Hb Paksé in Southeast Asian populations.
    Singsanan S, Fucharoen G, Savongsy O, Sanchaisuriya K, Fucharoen S.
    Ann Hematol; 2007 Sep; 86(9):665-9. PubMed ID: 17589844
    [Abstract] [Full Text] [Related]

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

  • 5. 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
    [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 Sep; 29(2):133-40. PubMed ID: 15921165
    [Abstract] [Full Text] [Related]

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

  • 8. Genetic origin of Hb D-Los Angeles [beta121(GH4)Glu-->Gln, GAA-->CAA] according to the beta-globin gene cluster haplotypes.
    Atalay EO, Atalay A, Ustel E, Yildiz S, Oztürk O, Köseler A, Bahadir A.
    Hemoglobin; 2007 Sep; 31(3):387-91. PubMed ID: 17654078
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 10. 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 Mar; 31(1):105-8. PubMed ID: 17365012
    [Abstract] [Full Text] [Related]

  • 11. Multi centric origin of Hb D-Punjab [beta121(GH4)Glu-->Gln, GAA>CAA].
    Yavarian M, Karimi M, Paran F, Neven C, Harteveld CL, Giordano PC.
    Hemoglobin; 2009 Mar; 33(6):399-405. PubMed ID: 19958184
    [Abstract] [Full Text] [Related]

  • 12. Molecular evidences of single mutational events followed by recurrent crossing-overs in the common delta-globin alleles in the Mediterranean area.
    Lacerra G, Musollino G, Scarano C, Lagona LF, Caruso DG, Testa R, Prezioso R, Di Noce F, Medulla E, Friscia MG, Mastrullo L, Caldora M, Nota L, Gaudiano C, Magnano C, Ciaccio C, Romeo MA, Carestia C.
    Gene; 2008 Feb 29; 410(1):129-38. PubMed ID: 18221842
    [Abstract] [Full Text] [Related]

  • 13. [Alpha 2 codon 30 deletion (deltaGAG) causing non-deletional hemoglobin H disease in Guangxi province].
    Chen P, Li SQ, Wu H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct 29; 21(5):435-9. PubMed ID: 15476164
    [Abstract] [Full Text] [Related]

  • 14. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis.
    Fucharoen S, Fucharoen G, Sae-ung N, Sanchaisuriya K.
    Blood Cells Mol Dis; 2007 Oct 29; 39(2):195-8. PubMed ID: 17587614
    [Abstract] [Full Text] [Related]

  • 15. 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 29; 75(3):157-63. PubMed ID: 14978697
    [Abstract] [Full Text] [Related]

  • 16. [Homozygous hemoglobin constant spring in Guangxi province].
    Chen P, Long GF, Lin WX, Li SQ.
    Zhonghua Xue Ye Xue Za Zhi; 2004 Apr 29; 25(4):205-8. PubMed ID: 15182556
    [Abstract] [Full Text] [Related]

  • 17. Molecular basis of Hb H disease in southwest Iran.
    Yavarian M, Karimi M, Zorai A, Harteveld CL, Giordano PC.
    Hemoglobin; 2005 Apr 29; 29(1):43-50. PubMed ID: 15768554
    [Abstract] [Full Text] [Related]

  • 18. 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 Apr 29; 34(6):582-6. PubMed ID: 21077767
    [Abstract] [Full Text] [Related]

  • 19. Screening for Hb Constant Spring in the Guangdong Province, South China, using the Sebia capillary electrophoresis system.
    Liao C, Zhou JY, Xie XM, Li DZ.
    Hemoglobin; 2011 Apr 29; 35(1):87-90. PubMed ID: 21250886
    [Abstract] [Full Text] [Related]

  • 20. Association of mild and severely unstable alpha chain variants: the first observation of a compound heterozygote with Hb Setif [alpha94(G1)Asp-->Tyr (alpha2)] and Hb Agrinio [alpha29(B10)Leu-->Pro (alpha2)] in a Greek family.
    Douna V, Papassotiriou I, Stamoulakatou A, Metaxotou-Mavrommati A, Kanavakis E, Traeger-Synodinos J.
    Hemoglobin; 2008 Apr 29; 32(6):592-5. PubMed ID: 19065338
    [Abstract] [Full Text] [Related]

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