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Journal Abstract Search

410 related items for PubMed ID: 27387985

  • 1. Haemoglobinopathies that occur with decreased HbA2 levels: a gene mutation set involving the δ gene at a Spanish centre.
    Villegas A, González FA, Nieto JM, de la Fuente-Gonzalo F, Martínez R, Torrejón MJ, Ropero P.
    J Clin Pathol; 2017 Jan; 70(1):75-80. PubMed ID: 27387985
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  • 2. [Delta⁰-thalassemia by insertion of 27 base pairs in δ-globin gene with decreased hemoglobin A₂ levels].
    González Borrachero ML, de la Fuente-Gonzalo F, González FA, Nieto JM, Villegas A, Ropero P.
    Med Clin (Barc); 2015 Apr 08; 144(7):312-6. PubMed ID: 25579773
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  • 3. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.
    Azma RZ, Othman A, Azman N, Alauddin H, Ithnin A, Yusof N, Razak NF, Sardi NH, Hussin NH.
    Malays J Pathol; 2012 Jun 08; 34(1):57-62. PubMed ID: 22870600
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  • 5. Effects of α-thalassaemia mutations on the haematological parameters of β-thalassaemia carriers.
    Saleh-Gohari N, Khademi Bami M, Nikbakht R, Karimi-Maleh H.
    J Clin Pathol; 2015 Jul 08; 68(7):562-6. PubMed ID: 25935548
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  • 10. HbA2 levels in β-thalassaemia carriers with the Filipino β0-deletion: are the levels higher than what is found with non-deletional forms of β0-thalassaemia?
    George E, Teh LK, Tan J, Lai MI, Wong L.
    Pathology; 2013 Jan 08; 45(1):62-5. PubMed ID: 23222244
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  • 12. First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.
    Amirian A, Karimipoor M, Jafarinejad M, Taghavi M, Kordafshari A, Fathi Azar S, Mohammadi MS, Zeinali S.
    Arch Iran Med; 2011 Jan 08; 14(1):8-11. PubMed ID: 21194254
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  • 13. Measurement of HbA₂ by capillary electrophoresis for diagnosing β-thalassemia/HbE disease in patients with low HbF.
    Prasing W, Pornprasert S.
    Lab Med; 2014 Jan 08; 45(3):226-30. PubMed ID: 25051074
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  • 15. Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations.
    Kasmi C, Amri Y, Hadj-Fredj S, Oueslati S, Dabboussi M, Mahjoub R, Hammami S, Aljane I, Mami FB, Jamoussi H, Messaoud T, Bibi A.
    Mol Biol Rep; 2021 Aug 08; 48(8):5923-5933. PubMed ID: 34341901
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  • 18. A comparative evaluation of the analytical performances of premier resolution-high-performance liquid chromatography (PR-HPLC) with capillary zone electrophoresis (CZE) assays for the detection of hemoglobin variants and the quantitation of HbA0, A2, E, and F.
    Laksap S, Suanboon S, Punyamung M, Ruengdit C, Pornprasert S.
    Clin Chem Lab Med; 2024 Jun 25; 62(7):1383-1392. PubMed ID: 38197862
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  • 20. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.
    Eur J Haematol; 2007 Nov 25; 79(5):422-8. PubMed ID: 17916081
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