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455 related items for PubMed ID: 26319530

  • 1. Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genes.
    Mehta PR, Upadhye DS, Sawant PM, Gorivale MS, Nadkarni AH, Shanmukhaiah C, Ghosh K, Colah RB.
    Ann Hematol; 2015 Dec; 94(12):1953-8. PubMed ID: 26319530
    [Abstract] [Full Text] [Related]

  • 2. 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 Dec; 39(3):201-6. PubMed ID: 26084319
    [Abstract] [Full Text] [Related]

  • 3. The carrier frequency of α-globin gene triplication in an Iranian population with normal or borderline hematological parameters.
    Moosavi SF, Amirian A, Zarbakhsh B, Kordafshari A, Mirzahoseini H, Zeinali S, Karimipoor M.
    Hemoglobin; 2011 Dec; 35(4):323-30. PubMed ID: 21797699
    [Abstract] [Full Text] [Related]

  • 4. [Molecular diagnosis in a Korean family with thalassemia intermedia due to co-inheritance of triplicated alpha-globin genes (alphaalpha/alphaalphaalpha(anti 3.7)) and beta-thalassemia trait (IVS-II-1 G-->A)].
    Chen M, Han JY, Sun Q, Kim IH, Ren Z, Huang S, Zeng Y.
    Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):195-7. PubMed ID: 11876981
    [Abstract] [Full Text] [Related]

  • 5. Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
    Colah R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Surve R, Subramaniam PG, Bondge N, Pujari K, Ghosh K, Mohanty D.
    Blood Cells Mol Dis; 2004 Apr; 33(2):153-7. PubMed ID: 15315795
    [Abstract] [Full Text] [Related]

  • 6. [Molecular diagnosis of beta-thalassemia intermedia].
    Chen J, Liu W, Chen M.
    Zhonghua Yi Xue Za Zhi; 1997 Aug; 77(8):575-8. PubMed ID: 9772460
    [Abstract] [Full Text] [Related]

  • 7. Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patients.
    Harteveld CL, Refaldi C, Cassinerio E, Cappellini MD, Giordano PC.
    Blood Cells Mol Dis; 2008 Aug; 40(3):312-6. PubMed ID: 18249014
    [Abstract] [Full Text] [Related]

  • 8. [Heterozygous β thalassemia with triplication of the α globin gene].
    Constanço MC, Rocha P, Bento C, Silva HM.
    Acta Med Port; 2011 Aug; 24(4):633-6. PubMed ID: 22521023
    [Abstract] [Full Text] [Related]

  • 9. Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients.
    Al-Nafie AN, Borgio JF, AbdulAzeez S, Al-Suliman AM, Qaw FS, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Ali RA, AlKhalifah MA, Al-Muhanna F, Steinberg MH, Al-Ali AK.
    Blood Cells Mol Dis; 2015 Jun; 55(1):27-9. PubMed ID: 25976463
    [Abstract] [Full Text] [Related]

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  • 11. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
    Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK.
    Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
    [Abstract] [Full Text] [Related]

  • 12. Association of an α-globin gene cluster duplication and heterozygous β-thalassemia in a patient with a severe thalassemia syndrome.
    Jiang H, Liu S, Zhang YL, Wan JH, Li R, Li DZ.
    Hemoglobin; 2015 Nov; 39(2):102-6. PubMed ID: 25690803
    [Abstract] [Full Text] [Related]

  • 13. Frequency of alpha-globin gene triplications and their interaction with beta-thalassemia mutations.
    Giordano PC, Bakker-Verwij M, Harteveld CL.
    Hemoglobin; 2009 Nov; 33(2):124-31. PubMed ID: 19373588
    [Abstract] [Full Text] [Related]

  • 14. The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies.
    Traeger-Synodinos J, Kanavakis E, Vrettou C, Maragoudaki E, Michael T, Metaxotou-Mavromati A, Kattamis C.
    Br J Haematol; 1996 Dec; 95(3):467-71. PubMed ID: 8943886
    [Abstract] [Full Text] [Related]

  • 15. Transfusion requirements and complication rate in β-thalassemia intermedia due to heterozygous β-globin gene mutation and triplicated α-globin genes.
    Bonello-Palot N, Benoit A, Agouti I, Hamouda I, Brousse V, NaThalY NetworkRegistre NaThalY, AP-HM, Marseille, France., Badens C.
    Eur J Haematol; 2023 Nov; 111(5):742-747. PubMed ID: 37519097
    [Abstract] [Full Text] [Related]

  • 16. Clinical phenotype of triplicated alpha-globin genes and heterozygosity for beta0-thalassemia in Chinese subjects.
    Ma SK, Au WY, Chan AY, Chan LC.
    Int J Mol Med; 2001 Aug; 8(2):171-5. PubMed ID: 11445869
    [Abstract] [Full Text] [Related]

  • 17. [Genotype of thalassemia genes and the polymorphism of β- globin gene in Cantonese].
    Liu L, Jiang WY, Xu SY, Chen J, Chen LM, Tian QH, Wang JC.
    Zhonghua Xue Ye Xue Za Zhi; 2013 Jul; 34(7):595-9. PubMed ID: 23906453
    [Abstract] [Full Text] [Related]

  • 18. Silent thalassemias: genotypes and phenotypes.
    Bianco I, Cappabianca MP, Foglietta E, Lerone M, Deidda G, Morlupi L, Grisanti P, Ponzini D, Rinaldi S, Graziani B.
    Haematologica; 1997 Jul; 82(3):269-80. PubMed ID: 9234571
    [Abstract] [Full Text] [Related]

  • 19. Analyzing 5'HS3 and 5'HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutations.
    Neishabury M, Azarkeivan A, Oberkanins C, Abedini SS, Zamani S, Najmabadi H.
    Blood Cells Mol Dis; 2011 Mar 15; 46(3):201-5. PubMed ID: 21232998
    [Abstract] [Full Text] [Related]

  • 20. [Thalassemia intermedia caused by interaction of IVS-1 1(G--A) mutation in the beta-globin gene and heterozygotic triplication in the alpha-globin gene].
    Martínez-López J, Galán García P, del Río E, Baiget M, Gilsanz Rodríguez F.
    Rev Clin Esp; 1998 Mar 15; 198(3):153-5. PubMed ID: 9586437
    [Abstract] [Full Text] [Related]

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