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Journal Abstract Search

180 related items for PubMed ID: 30520510

  • 1. New variants in beta globin gene among the Palestinian refugees with sickle cell disease in Lebanon.
    Moussa EY, Yassine NM, Borjac JM.
    Saudi Med J; 2018 Dec; 39(12):1253-1258. PubMed ID: 30520510
    [Abstract] [Full Text] [Related]

  • 2. Sickle cell disease in the Kurdish population of northern Iraq.
    Al-Allawi NA, Jalal SD, Nerwey FF, Al-Sayan GO, Al-Zebari SS, Alshingaly AA, Markous RD, Jubrael JM, Hamamy H.
    Hemoglobin; 2012 Dec; 36(4):333-42. PubMed ID: 22686351
    [Abstract] [Full Text] [Related]

  • 3. HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype-phenotype correlation.
    Notarangelo LD, Agostini A, Casale M, Samperi P, Arcioni F, Gorello P, Perrotta S, Masera N, Barone A, Bertoni E, Bonetti E, Burnelli R, Casini T, Del Vecchio GC, Filippini B, Giona F, Giordano P, Gorio C, Marchina E, Nardi M, Petrone A, Colombatti R, Sainati L, Russo G.
    Eur J Haematol; 2020 Mar; 104(3):214-222. PubMed ID: 31788855
    [Abstract] [Full Text] [Related]

  • 4. Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease.
    Thein SL.
    Adv Exp Med Biol; 2017 Mar; 1013():27-57. PubMed ID: 29127676
    [Abstract] [Full Text] [Related]

  • 5. β-globin gene cluster haplotypes in a cohort of 221 children with sickle cell anemia or Sβ⁰-thalassemia and their association with clinical and hematological features.
    Belisário AR, Martins ML, Brito AM, Rodrigues CV, Silva CM, Viana MB.
    Acta Haematol; 2010 Mar; 124(3):162-70. PubMed ID: 20938172
    [Abstract] [Full Text] [Related]

  • 6. Molecular biology of hemoglobin: its application to sickle cell anemia and thalassemia.
    Kan YW.
    Schweiz Med Wochenschr Suppl; 1991 Mar; 43():51-4. PubMed ID: 1726857
    [Abstract] [Full Text] [Related]

  • 7. Therapeutic hemoglobin levels after gene transfer in β-thalassemia mice and in hematopoietic cells of β-thalassemia and sickle cells disease patients.
    Breda L, Casu C, Gardenghi S, Bianchi N, Cartegni L, Narla M, Yazdanbakhsh K, Musso M, Manwani D, Little J, Gardner LB, Kleinert DA, Prus E, Fibach E, Grady RW, Giardina PJ, Gambari R, Rivella S.
    PLoS One; 2012 Mar; 7(3):e32345. PubMed ID: 22479321
    [Abstract] [Full Text] [Related]

  • 8. 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 Mar; 29(2):119-32. PubMed ID: 15921164
    [Abstract] [Full Text] [Related]

  • 9. Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and β-Thalassemia Patients.
    Pecoraro A, Troia A, Calzolari R, Scazzone C, Rigano P, Martorana A, Sacco M, Maggio A, Di Marzo R.
    Hemoglobin; 2015 Mar; 39(4):225-9. PubMed ID: 26016899
    [Abstract] [Full Text] [Related]

  • 10. Sickle cell/β-thalassemia: Comparison of Sβ0 and Sβ+ Brazilian patients followed at a single institution.
    Benites BD, Bastos SO, Baldanzi G, Dos Santos AO, Ramos CD, Costa FF, Gilli SC, Saad ST.
    Hematology; 2016 Dec; 21(10):623-629. PubMed ID: 27237196
    [Abstract] [Full Text] [Related]

  • 11. Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region.
    Amid A, Cheong M, Eng B, Hanna M, Hohenadel BA, Nakamura LM, Walker L, Odame I, Kirby-Allen M, Waye JS.
    Haematologica; 2015 May; 100(5):e166-8. PubMed ID: 25682598
    [No Abstract] [Full Text] [Related]

  • 12. Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotype.
    Daniel Y, Hill K, Inusa B, Thein SL, Howard J.
    Hemoglobin; 2011 May; 35(4):406-10. PubMed ID: 21797706
    [Abstract] [Full Text] [Related]

  • 13.
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  • 14. Genetic predisposition to β-thalassemia and sickle cell anemia in Turkey: a molecular diagnostic approach.
    Basak AN, Tuzmen S.
    Methods Mol Biol; 2011 May; 700():291-307. PubMed ID: 21204041
    [Abstract] [Full Text] [Related]

  • 15. Variations in the β-globin genes of sickle cell anaemia patients in Zaria, Northwestern, Nigeria.
    Awwalu S, Mamman AI, Hassan A, Dogara LG, Waziri AD, Aminu SM, Musa AU, Bello-Manga H.
    Niger J Clin Pract; 2017 Apr; 20(4):464-469. PubMed ID: 28406128
    [Abstract] [Full Text] [Related]

  • 16. Phenotypic effect of α-globin gene numbers on Indian sickle β-thalassemia patients.
    Pandey SK, Pandey S, Ranjan R, Shah V, Mishra RM, Sharma M, Saxena R.
    J Clin Lab Anal; 2014 Mar; 28(2):110-3. PubMed ID: 24395608
    [Abstract] [Full Text] [Related]

  • 17. beta(S)-Globin gene cluster haplotypes in the West Bank of Palestine.
    Samarah F, Ayesh S, Athanasiou M, Christakis J, Vavatsi N.
    Hemoglobin; 2009 Mar; 33(2):143-9. PubMed ID: 19373591
    [Abstract] [Full Text] [Related]

  • 18. 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; 14(1):8-11. PubMed ID: 21194254
    [Abstract] [Full Text] [Related]

  • 19. The molecular characterization of Beta globin gene in thalassemia patients reveals rare and a novel mutations in Pakistani population.
    Yasmeen H, Toma S, Killeen N, Hasnain S, Foroni L.
    Eur J Med Genet; 2016 Aug; 59(8):355-62. PubMed ID: 27263053
    [Abstract] [Full Text] [Related]

  • 20. Association of Xmn1 -158 γG variant with severity and HbF levels in β-thalassemia major and sickle cell anaemia.
    Dadheech S, Jain S, Madhulatha D, Sharma V, Joseph J, Jyothy A, Munshi A.
    Mol Biol Rep; 2014 May; 41(5):3331-7. PubMed ID: 24488321
    [Abstract] [Full Text] [Related]

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