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230 related items for PubMed ID: 28643346

  • 1. Red blood cells free α-haemoglobin pool: a biomarker to monitor the β-thalassemia intermedia variability. The ALPHAPOOL study.
    Vasseur C, Domingues-Hamdi E, Ledudal K, Le Corvoisier P, Barau C, Ghaleh B, Rialland A, Pissard S, Galactéros F, Baudin-Creuza V.
    Br J Haematol; 2017 Oct; 179(1):142-153. PubMed ID: 28643346
    [Abstract] [Full Text] [Related]

  • 2. 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; 38(5):335-8. PubMed ID: 25238043
    [Abstract] [Full Text] [Related]

  • 3. Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia.
    Farashi S, Bayat N, Faramarzi Garous N, Ashki M, Montajabi Niat M, Vakili S, Imanian H, Zeinali S, Najmabadi H, Azarkeivan A.
    Hemoglobin; 2015 Oct; 39(3):201-6. PubMed ID: 26084319
    [Abstract] [Full Text] [Related]

  • 4. 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; 44(5):349-353. PubMed ID: 33023363
    [Abstract] [Full Text] [Related]

  • 5. 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 Sep; 40(2):75-84. PubMed ID: 26635043
    [Abstract] [Full Text] [Related]

  • 6. Mild Thalassemia Intermedia Due to Interaction of δβ-Thalassemia with Triplicated α-Globin Genes.
    Payán-Pernía S, Bernal Noguera S, Rojas Rodríguez E, Serra Ferrer M, Remacha Sevilla ÁF.
    Hemoglobin; 2020 Jul; 44(4):294-296. PubMed ID: 32693657
    [Abstract] [Full Text] [Related]

  • 7. Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran.
    Miri-Moghaddam E, Bahrami S, Naderi M, Bazi A, Karimipoor M.
    Hemoglobin; 2016 Jun; 40(3):173-8. PubMed ID: 27117567
    [Abstract] [Full Text] [Related]

  • 8. The phenomena of balanced effect between α-globin gene and of β-globin gene.
    Zhong L, Gan X, Xu L, Liang C, Xie Y, Lin W, Chen P, Liu M.
    BMC Med Genet; 2018 Aug 17; 19(1):145. PubMed ID: 30119651
    [Abstract] [Full Text] [Related]

  • 9. Molecular spectrum of α- and β-globin gene mutations detected in the population of Guangxi Zhuang Autonomous Region, People's Republic of China.
    Zheng CG, Liu M, Du J, Chen K, Yang Y, Yang Z.
    Hemoglobin; 2011 Aug 17; 35(1):28-39. PubMed ID: 21250879
    [Abstract] [Full Text] [Related]

  • 10. Genetic determinants of β-thalassemia intermedia in Pakistan.
    Khan J, Ahmad N, Siraj S, Hoti N.
    Hemoglobin; 2015 Aug 17; 39(2):95-101. PubMed ID: 25707679
    [Abstract] [Full Text] [Related]

  • 11. 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 17; 43(1):66-68. PubMed ID: 30843739
    [Abstract] [Full Text] [Related]

  • 12. Molecular basis of thalassemia intermedia in Iran.
    Akbari MT, Izadi P, Izadyar M, Kyriacou K, Kleanthous M.
    Hemoglobin; 2008 Jan 17; 32(5):462-70. PubMed ID: 18932071
    [Abstract] [Full Text] [Related]

  • 13. [Analysis of hematological characteristics on the 79 co-inheritance of α-thalassemia and β-thalassemia carriers in Guangxi].
    Xiong F, Lou JW, Wei XF, Sun MN, Huang JW, Shang X, Zhang XH, Xu XM.
    Zhonghua Xue Ye Xue Za Zhi; 2012 Oct 17; 33(10):856-60. PubMed ID: 23384911
    [Abstract] [Full Text] [Related]

  • 14. Evaluation of the free α-hemoglobin pool in red blood cells: a new test providing a scale of β-thalassemia severity.
    Vasseur C, Pissard S, Domingues-Hamdi E, Marden MC, Galactéros F, Baudin-Creuza V.
    Am J Hematol; 2011 Feb 17; 86(2):199-202. PubMed ID: 21264907
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  • 19. The role of heterocellular hereditary persistence of fetal haemoglobin in beta(0)-thalassaemia intermedia.
    Chang YP, Littera R, Garau R, Smith KD, Dover GJ, Iannelli S, Cacace E, Contu L.
    Br J Haematol; 2001 Sep 17; 114(4):899-906. PubMed ID: 11564083
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