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666 related items for PubMed ID: 17994378

  • 1. Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.
    Verma IC, Kleanthous M, Saxena R, Fucharoen S, Winichagoon P, Raizuddin S, Khan SN, Akbari MT, Izadyar M, Kotea N, Old JM, Ioannou PA, Khan B.
    Hemoglobin; 2007; 31(4):439-52. PubMed ID: 17994378
    [Abstract] [Full Text] [Related]

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

  • 3. 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; 38(5):335-8. PubMed ID: 25238043
    [Abstract] [Full Text] [Related]

  • 4. Molecular epidemiological study of alpha- and beta-thalassemia in Sihui city.
    Tan JR, Li WJ, Ma JY, Mo QH, Li LY, Jia SQ, Lao XW, Li LY, He RQ, Xu XM.
    Di Yi Jun Yi Da Xue Xue Bao; 2003 Jul; 23(7):716-9. PubMed ID: 12865230
    [Abstract] [Full Text] [Related]

  • 5. Genotypic correlation between six common beta-thalassemia mutations and the XmnI polymorphism in the Moroccan population.
    Agouti I, Badens C, Abouyoub A, Khattab M, Sayah F, Barakat A, Bennani M.
    Hemoglobin; 2007 Jul; 31(2):141-9. PubMed ID: 17486495
    [Abstract] [Full Text] [Related]

  • 6. 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 Jul; 42(1):32-5. PubMed ID: 18951049
    [Abstract] [Full Text] [Related]

  • 7. Homozygosity for a rare beta 0-thalassemia mutation [frameshift codons 25/26 (+T)] causes beta-thalassemia intermedia in an Iranian family.
    Haghi M, Feizi AA, Harteveld CL, Pouladi N, Feizi MA.
    Hemoglobin; 2009 Jul; 33(1):75-80. PubMed ID: 19205978
    [Abstract] [Full Text] [Related]

  • 8. Phenotypes of individuals with a beta thal classical allele associated either with a beta thal silent allele or with alpha globin gene triplication.
    Bianco I, Lerone M, Foglietta E, Deidda G, Cappabianca MP, Morlupi L, Ponzini D, Grisanti P, Di Biagio P, Amato A, Mezzabotta M, Graziani B.
    Haematologica; 1997 Jul; 82(5):513-25. PubMed ID: 9407714
    [Abstract] [Full Text] [Related]

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

  • 10. The spectrum of α- and β-thalassemia mutations in Yunnan Province of Southwestern China.
    Zhang J, Zhu BS, He J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH.
    Hemoglobin; 2012 Jul; 36(5):464-73. PubMed ID: 22943051
    [Abstract] [Full Text] [Related]

  • 11. 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; 79(5):422-8. PubMed ID: 17916081
    [Abstract] [Full Text] [Related]

  • 12. Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy.
    Siriratmanawong N, Chansri W, Singsanan S, Fucharoen G, Fucharoen S.
    Hemoglobin; 2009 Nov; 33(6):507-14. PubMed ID: 19958198
    [Abstract] [Full Text] [Related]

  • 13. 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 Nov; 35(1):28-39. PubMed ID: 21250879
    [Abstract] [Full Text] [Related]

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

  • 15. [Prevalence survey and molecular characterization of alpha and beta thalassemia in Liuzhou city of Guangxi].
    Cai R, Li L, Liang X, Liu Z, Su L, Li W, Zhu Q, Mo Q, Pan L, Ouyang H, Huang L, Xu X.
    Zhonghua Liu Xing Bing Xue Za Zhi; 2002 Aug; 23(4):281-5. PubMed ID: 12411074
    [Abstract] [Full Text] [Related]

  • 16. Molecular characterization of sickle cell anemia in the Northern Brazilian state of Pará.
    De Lemos Cardoso G, Guerreiro JF.
    Am J Hum Biol; 2010 Aug; 22(5):573-7. PubMed ID: 20737602
    [Abstract] [Full Text] [Related]

  • 17. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
    Efremov GD.
    Hemoglobin; 2007 Aug; 31(1):1-15. PubMed ID: 17365000
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Frequency of positive XmnIGgamma polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation.
    Neishabury M, Azarkeivan A, Najmabadi H.
    Blood Cells Mol Dis; 2010 Aug; 44(2):95-9. PubMed ID: 19892574
    [Abstract] [Full Text] [Related]

  • 20. 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]

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