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Journal Abstract Search

330 related items for PubMed ID: 28475397

  • 1. Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family.
    He S, Qin Q, Lin L, Chen Q, Yi S, Wei H, Du J, Zheng C, Qiu X, Chen B.
    Hemoglobin; 2017 Jan; 41(1):68-72. PubMed ID: 28475397
    [Abstract] [Full Text] [Related]

  • 2. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM.
    Hemoglobin; 2016 Jan; 40(2):75-84. PubMed ID: 26635043
    [Abstract] [Full Text] [Related]

  • 3. Complex Interaction of Hb Q-Thailand (HBA1: c.223G>C) with β-Thalassemia/Hb E (HBB: c.79G>A) Disease.
    Panyasai S, Satthakarn S, Pornprasert S.
    Hemoglobin; 2018 Jan; 42(1):54-57. PubMed ID: 29484903
    [Abstract] [Full Text] [Related]

  • 4. First Report of a Chinese Family Carrying a Double Heterozygosity for Hb Q-Thailand and Hb J-Bangkok.
    Jiang F, Zhou JY, Yan JM, Lu YC, Li DZ.
    Hemoglobin; 2016 Nov; 40(6):425-427. PubMed ID: 28361593
    [Abstract] [Full Text] [Related]

  • 5. 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 Nov; 37(2):197-200. PubMed ID: 23390935
    [Abstract] [Full Text] [Related]

  • 6. Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand.
    Panyasai S, Pornprasert S.
    Hemoglobin; 2020 May; 44(3):179-183. PubMed ID: 32482156
    [Abstract] [Full Text] [Related]

  • 7. Hb Westmead (HBA2: c.369C>G): Hematological Characteristics in Heterozygotes with and without α0-Thalassemia.
    Jiang F, Ju AP, Li J, Chen GL, Zhou JY, Tang XW, Zuo LD, Li DZ.
    Hemoglobin; 2020 May; 44(3):153-155. PubMed ID: 32436451
    [Abstract] [Full Text] [Related]

  • 8. Complex interaction of Hb Q-Thailand and Hb E with alpha(0)-thalassemia and hereditary persistence of fetal hemoglobin in a Chinese family.
    Zheng W, Liu Y, Chen D, Rong K, Ge Y, Gong C, Chen H.
    Ann Hematol; 2010 Sep; 89(9):883-8. PubMed ID: 20333523
    [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. Five hemoglobin variants in a double heterozygote for α- and β-globin chain defects.
    Singha K, Fucharoen G, Fucharoen S.
    Acta Haematol; 2014 Mar; 131(2):71-5. PubMed ID: 24081021
    [Abstract] [Full Text] [Related]

  • 11. 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; 23(3):187-191. PubMed ID: 28945175
    [Abstract] [Full Text] [Related]

  • 12. Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects.
    Fucharoen S, Fucharoen G.
    Hemoglobin; 2012 Apr; 36(1):18-24. PubMed ID: 22145566
    [Abstract] [Full Text] [Related]

  • 13. A Novel Mutation of the α2-Globin Gene Causing α+-Thalassemia: Hb Nanning (HBA2: c.369_370delinsGA).
    Chen B, Lin L, Yi S, Chen Q, Wei H, Li G, Zheng C, He S, Qiu X.
    Hemoglobin; 2017 Jan; 41(1):56-58. PubMed ID: 28395547
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

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  • 16. The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.
    Charoenkwan P, Teerachaimahit P, Sanguansermsri T.
    Hemoglobin; 2014 Oct 15; 38(5):335-8. PubMed ID: 25238043
    [Abstract] [Full Text] [Related]

  • 17. First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family.
    Murad H, Moassas F.
    Hemoglobin; 2019 Jan 15; 43(1):66-68. PubMed ID: 30843739
    [Abstract] [Full Text] [Related]

  • 18. Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A2 Levels.
    Satthakarn S, Panyasai S, Pornprasert S.
    Hemoglobin; 2020 Sep 15; 44(5):349-353. PubMed ID: 33023363
    [Abstract] [Full Text] [Related]

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  • 20. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
    Viprakasit V, Ekwattanakit S, Chalaow N, Riolueang S, Wijit S, Tanyut P, Chat-Uthai N, Tachavanich K.
    Acta Haematol; 2014 Sep 15; 131(2):88-94. PubMed ID: 24081251
    [Abstract] [Full Text] [Related]

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