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    Results: 1 to 20 of 107

    1.

    Screening for Hb Constant Spring in the Guangdong Province, South China, using the Sebia capillary electrophoresis system.

    Liao C, Zhou JY, Xie XM, Li DZ.

    Hemoglobin. 2011;35(1):87-90.

    PMID:
    21250886
    [PubMed - indexed for MEDLINE]
    2.

    β+-Thalassemia trait due to a novel mutation in the β-globin gene promoter: -26 (A>C) [HBB c.-76A>C].

    Waye JS, Nakamura-Garrett LM, Eng B, Kanavakis E, Traeger-Synodinos J.

    Hemoglobin. 2011;35(1):84-6.

    PMID:
    21250885
    [PubMed - indexed for MEDLINE]
    3.

    Characterization of the 5' and 3' breakpoints of the Spanish (δβ)0-thalassemia deletion in Mexican patients.

    Guzmán LF, Perea FJ, Morales-González KR, Sánchez-López JY, de la Cruz EI, Chávez-Velasco ML, Ibarra CB.

    Hemoglobin. 2011;35(1):80-3.

    PMID:
    21250884
    [PubMed - indexed for MEDLINE]
    4.

    Increased oxidative stress and iron overload in Jordanian β-thalassemic children.

    Abdalla MY, Fawzi M, Al-Maloul SR, El-Banna N, Tayyem RF, Ahmad IM.

    Hemoglobin. 2011;35(1):67-79.

    PMID:
    21250883
    [PubMed - indexed for MEDLINE]
    5.

    Novel and known microsatellite markers within the β-globin cluster to support robust preimplantation genetic diagnosis of β-thalassemia and sickle cell syndromes.

    Zachaki S, Vrettou C, Destouni A, Kokkali G, Traeger-Synodinos J, Kanavakis E.

    Hemoglobin. 2011;35(1):56-66.

    PMID:
    21250882
    [PubMed - indexed for MEDLINE]
    6.

    Prenatal diagnosis of β-thalassemia and other hemoglobinopathies in southwestern Turkey.

    Mendilcioglu I, Yakut S, Keser I, Simsek M, Yesilipek A, Bagci G, Luleci G.

    Hemoglobin. 2011;35(1):47-55.

    PMID:
    21250881
    [PubMed - indexed for MEDLINE]
    7.

    Genotype-phenotype correlation in Iranian patients with Hb H disease.

    Ebrahimkhani S, Azarkeivan A, Bayat N, Houry-Parvin M, Jalil-Nejad S, Zand S, Golkar Z, Hadavi V, Imanian H, Oberkanins C, Najmabadi H.

    Hemoglobin. 2011;35(1):40-6.

    PMID:
    21250880
    [PubMed - indexed for MEDLINE]
    8.

    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;35(1):28-39.

    PMID:
    21250879
    [PubMed - indexed for MEDLINE]
    9.

    Fetal hemoglobin response to hydroxyurea in Yemeni sickle cell disease patients.

    Al-Nood HA, Al-Khawlani MM, Al-Akwa A.

    Hemoglobin. 2011;35(1):13-21.

    PMID:
    21250877
    [PubMed - indexed for MEDLINE]
    10.

    Hb S-β-thalassemia: molecular, hematological and clinical comparisons.

    Serjeant GR, Serjeant BE, Fraser RA, Hambleton IR, Higgs DR, Kulozik AE, Donaldson A.

    Hemoglobin. 2011;35(1):1-12.

    PMID:
    21250876
    [PubMed - indexed for MEDLINE]
    11.

    Flow cytometric assessment of leukocyte function in sickle cell anemia.

    Qari MH, Zaki WA.

    Hemoglobin. 2011;35(4):367-81.

    PMID:
    21797704
    [PubMed - indexed for MEDLINE]
    13.

    Bilirubin peak can be mistaken as Hb Bart's or Hb H on High-performance liquid chromatography.

    Kar R, Sharma CB.

    Hemoglobin. 2011;35(2):171-4.

    PMID:
    21417577
    [PubMed - indexed for MEDLINE]
    14.

    Identification of a new α chain variant at codons 22-25 (-9 nts) using the Sebia capillarys 2 electrophoresis system.

    Liao C, Zhou JY, Xie XM, Liu YN, Chen LH, Li DZ.

    Hemoglobin. 2011;35(2):166-70.

    PMID:
    21417576
    [PubMed - indexed for MEDLINE]
    15.

    Hb A2 Hong Kong - A novel δ-globin variant in a Chinese family masks the diagnosis of β-thalassemia trait.

    So CC, Chan AY, Luo HY, Verhovsek M, Chui DH, Ling SC, Chan LC.

    Hemoglobin. 2011;35(2):162-5.

    PMID:
    21417575
    [PubMed - indexed for MEDLINE]
    16.

    A second observation of the rare frameshift mutation in the β-globin gene: codon 46 (+A) (Hbb:c.138_139insA).

    Ghedira ES, Dupin-Deguine D, Duffilot D, Lemetayer N, Faubert E, Pissard S.

    Hemoglobin. 2011;35(2):157-61.

    PMID:
    21417574
    [PubMed - indexed for MEDLINE]
    17.

    Two new hemoglobin variants: Hb Aix-Les-Bains [β5(A2)Pro→Leu; HBB:c.17 C>T] and Hb Dubai [α122(H5)His→Leu (α2); HBA2:c.368 A>T].

    Joly P, Garcia C, Lacan P, Couprie N, Francina A.

    Hemoglobin. 2011;35(2):147-51.

    PMID:
    21417572
    [PubMed - indexed for MEDLINE]
    18.

    Hb Lynwood [α107(G14) (-T) (α2) HBA2:c.323delT)] in conjunction with the α(3.7) deletion produces a moderately severe α-thalassemia phenotype.

    Finlayson J, Ghassemifar R, Holmes P, Grey D, Newbound C, Pell N, Jennens M, Macaulay C, Greenwood L, Beilby J.

    Hemoglobin. 2011;35(2):142-6.

    PMID:
    21417571
    [PubMed - indexed for MEDLINE]
    19.

    Spectrum of β-thalassemia mutations in the eastern province of Saudi Arabia.

    Al-Sultan A, Phanasgaonkar S, Suliman A, Al-Baqushi M, Nasrullah Z, Al-Ali A.

    Hemoglobin. 2011;35(2):125-34.

    PMID:
    21417569
    [PubMed - indexed for MEDLINE]
    20.

    Hb A2' (Hb B2) in the Omani population and diagnostic significance.

    Daar S, Al Zadjali S, Gravell D, Al Haddabi H, Al Riyami M, Al Belushi A, Berbar T, Krishnamoorthy R.

    Hemoglobin. 2011;35(2):117-24.

    PMID:
    21417568
    [PubMed - indexed for MEDLINE]

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