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562 related items for PubMed ID: 26984585

  • 1. Hemoglobinopathies in the Çukurova Region and Neighboring Provinces.
    Yuzbasioglu Ariyurek S, Yildiz SM, Yalin AE, Guzelgul F, Aksoy K.
    Hemoglobin; 2016 Jun; 40(3):168-72. PubMed ID: 26984585
    [Abstract] [Full Text] [Related]

  • 2. Epidemiology of Hemoglobinopathies in the Huzhou Region, Zhejiang Province, Southeast China.
    Ding ZY, Shen GS, Zhang S, He PY.
    Hemoglobin; 2016 Sep; 40(5):304-309. PubMed ID: 27615034
    [Abstract] [Full Text] [Related]

  • 3. β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey.
    Guzelgul F, Seydel GS, Aksoy K.
    Hemoglobin; 2020 Jul; 44(4):249-253. PubMed ID: 32664780
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  • 4. 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 Jul; 40(2):75-84. PubMed ID: 26635043
    [Abstract] [Full Text] [Related]

  • 5. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
    Efremov GD.
    Hemoglobin; 2007 Jul; 31(1):1-15. PubMed ID: 17365000
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  • 7. Molecular Epidemiology of Hemoglobinopathies in Cambodia.
    Munkongdee T, Tanakulmas J, Butthep P, Winichagoon P, Main B, Yiannakis M, George J, Devenish R, Fucharoen S, Svasti S.
    Hemoglobin; 2016 Jun; 40(3):163-7. PubMed ID: 27117566
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  • 8. Prevalence of β-thalassemia trait and abnormal hemoglobins in Sanliurfa Province in southeast Turkey.
    Incebiyik A, Genc A, Hilali NG, Camuzcuoglu A, Camuzcuoglu H, Kilic A, Vural M.
    Hemoglobin; 2014 Jun; 38(6):402-4. PubMed ID: 25405917
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  • 9. Comprehensive spectrum of the β-Thalassemia mutations in Khuzestan, southwest Iran.
    Galehdari H, Salehi B, Azmoun S, Keikhaei B, Zandian KM, Pedram M.
    Hemoglobin; 2010 Jun; 34(5):461-8. PubMed ID: 20854120
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  • 11. Molecular lesion frequency of hemoglobin gene disorders in Taiwan.
    Liu SC, Peng CT, Lin TH, Wang SJ, Shih MC, Tien N, Chang CC, Lu JJ, Lin CY.
    Hemoglobin; 2011 Jun; 35(3):228-36. PubMed ID: 21599435
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  • 15. Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India.
    Dehury S, Meher S, Patel S, Das K, Jana A, Bhattacharya S, Sahoo S, Sarkar B, Mohanty PK.
    Hemoglobin; 2019 Mar; 43(2):132-136. PubMed ID: 31190580
    [Abstract] [Full Text] [Related]

  • 16. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
    Moassas F, Nweder MS, Murad H.
    BMC Pediatr; 2019 Feb 18; 19(1):61. PubMed ID: 30777047
    [Abstract] [Full Text] [Related]

  • 17. Distinctive mutation spectrum of the HBB gene in an urban eastern Indian population.
    Sahoo SS, Biswal S, Dixit M.
    Hemoglobin; 2014 Feb 18; 38(1):33-8. PubMed ID: 24099628
    [Abstract] [Full Text] [Related]

  • 18. Hb A1c Determination by Capillary Electrophoresis is an Efficient Method for Detecting β-Thalassemias and Hemoglobin Variants.
    Orts JA, Zúñiga Á, Bello Y, Fabregat AB, Vicente AI.
    Hemoglobin; 2016 Sep 18; 40(5):335-340. PubMed ID: 27535164
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  • 19. Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients.
    Azarkeivan A, Cohan N, Niazkar HR, Azizi A, Rad F.
    Hemoglobin; 2020 Mar 18; 44(2):109-112. PubMed ID: 32370567
    [Abstract] [Full Text] [Related]

  • 20. Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects.
    Fucharoen S, Fucharoen G.
    Hemoglobin; 2012 Mar 18; 36(1):18-24. PubMed ID: 22145566
    [Abstract] [Full Text] [Related]

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