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643 related items for PubMed ID: 15315795

  • 1. 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; 33(2):153-7. PubMed ID: 15315795
    [Abstract] [Full Text] [Related]

  • 2. Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-beta-thalassemia in Northeast Thailand.
    Nuntakarn L, Fucharoen S, Fucharoen G, Sanchaisuriya K, Jetsrisuparb A, Wiangnon S.
    Blood Cells Mol Dis; 2009; 42(1):32-5. PubMed ID: 18951049
    [Abstract] [Full Text] [Related]

  • 3. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM, El-Khatib FF, Ayesh S.
    Hemoglobin; 2005; 29(2):119-32. PubMed ID: 15921164
    [Abstract] [Full Text] [Related]

  • 4. Molecular basis of β-thalassemia in the United Arab Emirates.
    Baysal E.
    Hemoglobin; 2011; 35(5-6):581-8. PubMed ID: 22074124
    [Abstract] [Full Text] [Related]

  • 5. Spectrum of beta-thalassemia mutations and their association with allelic sequence polymorphisms at the beta-globin gene cluster in an Eastern Indian population.
    Kukreti R, Dash D, E VK, Chakravarty S, Das SK, De M, Talukder G.
    Am J Hematol; 2002 Aug; 70(4):269-77. PubMed ID: 12210807
    [Abstract] [Full Text] [Related]

  • 6. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
    El-Gawhary S, El-Shafie S, Niazi M, Aziz M, El-Beshlawy A.
    Hemoglobin; 2007 Aug; 31(1):63-9. PubMed ID: 17365006
    [Abstract] [Full Text] [Related]

  • 7. Molecular heterogeneity of beta-thalassemia in Thailand.
    Fukumaki Y, Fucharoen S, Fucharoen G, Okamoto N, Ichinose M, Jetsrisuparb A, Sriroongrueng W, Nopparatana C, Laosombat V, Panich V.
    Southeast Asian J Trop Med Public Health; 1992 Aug; 23 Suppl 2():14-21. PubMed ID: 1363706
    [Abstract] [Full Text] [Related]

  • 8. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN.
    Hemoglobin; 2007 Aug; 31(2):233-41. PubMed ID: 17486506
    [Abstract] [Full Text] [Related]

  • 9. The spectrum of beta-thalassemia mutations in southern Thailand.
    Nopparatana C, Panich V, Saechan V, Sriroongrueng V, Nopparatana C, Rungjeadpha J, Pornpatkul M, Laosombat V, Fukumaki Y.
    Southeast Asian J Trop Med Public Health; 1995 Aug; 26 Suppl 1():229-34. PubMed ID: 8629112
    [Abstract] [Full Text] [Related]

  • 10. Molecular analysis of beta-thalassemia in South Vietnam.
    Svasti S, Hieu TM, Munkongdee T, Winichagoon P, Van Be T, Van Binh T, Fucharoen S.
    Am J Hematol; 2002 Oct; 71(2):85-8. PubMed ID: 12353305
    [Abstract] [Full Text] [Related]

  • 11. Variable clinical severity of Hb E beta-thalassemia among Indians.
    Nadkarni A, Ghosh K, Gorakshakar A, Colah R, Mohanty D.
    J Assoc Physicians India; 1999 Oct; 47(10):966-8. PubMed ID: 10778688
    [Abstract] [Full Text] [Related]

  • 12. Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.
    Bibi A, Messaoud T, Fattoum S.
    Hemoglobin; 2006 Oct; 30(2):175-81. PubMed ID: 16798642
    [Abstract] [Full Text] [Related]

  • 13. Nucleotide -88 (C-T) promoter mutation is a common beta-thalassemia mutation in the Jat Sikhs of Punjab, India.
    Garewal G, Das R, Ahluwalia J, Marwaha RK, Varma S.
    Am J Hematol; 2005 Aug; 79(4):252-6. PubMed ID: 16044458
    [Abstract] [Full Text] [Related]

  • 14. Evaluation of the genetic basis of phenotypic heterogeneity in north Indian patients with thalassemia major.
    Sharma N, Das R, Kaur J, Ahluwalia J, Trehan A, Bansal D, Panigrahi I, Marwaha RK.
    Eur J Haematol; 2010 Jun; 84(6):531-7. PubMed ID: 20132300
    [Abstract] [Full Text] [Related]

  • 15. Detection of beta-thalassemia mutations using a multiplex amplification refractory mutation system assay.
    Mirasena S, Shimbhu D, Sanguansermsri M, Sanguansermsri T.
    Hemoglobin; 2008 Jun; 32(4):403-9. PubMed ID: 18654891
    [Abstract] [Full Text] [Related]

  • 16. Identification of three novel mutations [-41 (A>C), codon 24 (-G), and IVS-I-109 (-T)], in a study of beta-thalassemia alleles in the Isfahan region of Iran.
    Salehi R, Fisher CA, Bignell PA, Eslami G, Old JM.
    Hemoglobin; 2010 Jun; 34(1):115-20. PubMed ID: 20113296
    [Abstract] [Full Text] [Related]

  • 17. The molecular analysis of beta-thalassemia mutations in Lorestan Province, Iran.
    Kiani AA, Mortazavi Y, Zeinali S, Shirkhani Y.
    Hemoglobin; 2007 Jun; 31(3):343-9. PubMed ID: 17654071
    [Abstract] [Full Text] [Related]

  • 18. The molecular heterogeneity of beta-thalassemia in Greece.
    Boussiou M, Karababa P, Sinopoulou K, Tsaftaridis P, Plata E, Loutradi-Anagnostou A.
    Blood Cells Mol Dis; 2008 Jun; 40(3):317-9. PubMed ID: 18096416
    [Abstract] [Full Text] [Related]

  • 19. The clinical severity of beta-thalassemia mutations in West Malaysia.
    George E.
    Southeast Asian J Trop Med Public Health; 1995 Jun; 26 Suppl 1():225-8. PubMed ID: 8629111
    [Abstract] [Full Text] [Related]

  • 20. 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]

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