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    Results: 1 to 20 of 26

    1.

    Comment on: Neutropenia and anemia with reduced serum vitamin B(12).

    Kamel S, Lu Z, Sikaris K.

    Am J Hematol. 2011 Oct 20. doi: 10.1002/ajh.22226. [Epub ahead of print] No abstract available.

    PMID:
    22189831
    [PubMed - as supplied by publisher]

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    2.

    New anemia therapies: translating novel strategies from bench to bedside.

    Macdougall IC.

    Am J Kidney Dis. 2012 Mar;59(3):444-51. Epub 2011 Dec 21. Review.

    PMID:
    22192713
    [PubMed - indexed for MEDLINE]

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    3.

    Extensive admixture in Brazilian sickle cell patients: implications for the mapping of genetic modifiers.

    da Silva MC, Zuccherato LW, Lucena FC, Soares-Souza GB, Vieira ZM, Pena SD, Martins ML, Tarazona-Santos E.

    Blood. 2011 Oct 20;118(16):4493-5; author reply 4495. No abstract available.

    PMID:
    22021456
    [PubMed - indexed for MEDLINE]

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    4.

    Is there still a place for myeloablative regimen to transplant young adults with sickle cell disease?

    Kuentz M, Robin M, Dhedin N, Hicheri Y, de Latour RP, Rohrlich P, Bordigoni P, Bruno B, Socié G, Bernaudin F.

    Blood. 2011 Oct 20;118(16):4491-2; author reply 4492-3. No abstract available.

    PMID:
    22021455
    [PubMed - indexed for MEDLINE]

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    5.

    HbA(2): at the borderline of the KLF.

    Gallagher PG.

    Blood. 2011 Oct 20;118(16):4301-2. No abstract available.

    PMID:
    22021451
    [PubMed - indexed for MEDLINE]

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    6.

    KLF1 gene mutations cause borderline HbA(2).

    Perseu L, Satta S, Moi P, Demartis FR, Manunza L, Sollaino MC, Barella S, Cao A, Galanello R.

    Blood. 2011 Oct 20;118(16):4454-8. Epub 2011 Aug 5.

    PMID:
    21821711
    [PubMed - indexed for MEDLINE]

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    7.

    β-thalassemia: a model for elucidating the dynamic regulation of ineffective erythropoiesis and iron metabolism.

    Ginzburg Y, Rivella S.

    Blood. 2011 Oct 20;118(16):4321-30. Epub 2011 Jul 18. Review.

    PMID:
    21768301
    [PubMed - indexed for MEDLINE]

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    8.

    Exome sequencing identifies MPL as a causative gene in familial aplastic anemia.

    Walne AJ, Dokal A, Plagnol V, Beswick R, Kirwan M, de la Fuente J, Vulliamy T, Dokal I.

    Haematologica. 2012 Apr;97(4):524-8. Epub 2011 Dec 16.

    PMID:
    22180433
    [PubMed - in process]
    Free PMC Article

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    9.

    Long-term follow up after allogeneic stem cell transplantation in patients with severe aplastic anemia after cyclophosphamide plus antithymocyte globulin conditioning.

    Konopacki J, Porcher R, Robin M, Bieri S, Cayuela JM, Larghero J, Xhaard A, Andreoli AL, Dhedin N, Petropoulou A, Rodriguez-Otero P, Ribaud P, Moins-Teisserenc H, Carmagnat M, Toubert A, Chalandon Y, Socie G, Peffault de Latour R.

    Haematologica. 2012 May;97(5):710-6. Epub 2011 Dec 16.

    PMID:
    22180425
    [PubMed - in process]
    Free PMC Article

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    10.

    Malignancies in β-thalassemia patients: first description of two cases of thyroid cancer and review of the literature.

    Poggi M, Sorrentino F, Pascucci C, Monti S, Lauri C, Bisogni V, Toscano V, Cianciulli P.

    Hemoglobin. 2011;35(4):439-46. Review.

    PMID:
    21797713
    [PubMed - indexed for MEDLINE]

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    11.

    Early prenatal diagnosis of thalassemia: the first report of experience in mainland China.

    Liao C, Pan M, Han J, Yang X, Li J, Li R, Li DZ.

    Hemoglobin. 2011;35(4):434-8.

    PMID:
    21797712
    [PubMed - indexed for MEDLINE]

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    12.

    Hb Lake Tapawingo [α46(CE4)Phe→Ser; HBA2:c.140T>C]: a new unstable α chain hemoglobin variant associated with low systemic arterial saturation.

    Guest EM, Neville KA, Hoyer JD, Safo MK, Garg U, Saunders CJ, Abdulmalik O, Zwick DL.

    Hemoglobin. 2011;35(4):411-6.

    PMID:
    21797707
    [PubMed - indexed for MEDLINE]

    Related citations

    13.

    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;35(4):406-10.

    PMID:
    21797706
    [PubMed - indexed for MEDLINE]

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    14.

    Clinicopathological and radiological study of Egyptian β-thalassemia intermedia and β-thalassemia major patients: relation to complications and response to therapy.

    Mokhtar GM, Tantawy AA, Adly AA, Ismail EA.

    Hemoglobin. 2011;35(4):382-405.

    PMID:
    21797705
    [PubMed - indexed for MEDLINE]

    Related citations

    15.

    Molecular analysis of β-thalassemia patients: first identification of mutations HBB:c.93-2A>G and HBB:c.114G>A in Brazil.

    Fernandes AC, Shimmoto MM, Furuzawa GK, Vicari P, Figueiredo MS.

    Hemoglobin. 2011;35(4):358-66.

    PMID:
    21797703
    [PubMed - indexed for MEDLINE]

    Related citations

    16.

    Molecular basis of β-thalassemia in the western province of Saudi Arabia: identification of rare β-thalassemia mutations.

    Abuzenadah AM, Hussein IM, Damanhouri GA, A-Sayes FM, Gari MA, Chaudhary AG, Zaher GF, Al-Attas A, Al-Qahtani MH.

    Hemoglobin. 2011;35(4):346-57.

    PMID:
    21797702
    [PubMed - indexed for MEDLINE]

    Related citations

    17.

    Comparison between capillary electrophoresis and high performance liquid chromatography for detection and quantification of Hb constant spring [Hb CS; α142, Term→Gln (TAA>CAA IN α2)].

    Waneesorn J, Panyasai S, Kongthai K, Singboottra P, Pornprasert S.

    Hemoglobin. 2011;35(4):338-45.

    PMID:
    21797701
    [PubMed - indexed for MEDLINE]

    Related citations

    18.

    β-Thalassemia mutations found during 1 year of prenatal diagnoses in Fars Province, Iran.

    Rahiminejad MS, Zeinali S, Afrasiabi A, Valeshabad AK.

    Hemoglobin. 2011;35(4):331-7.

    PMID:
    21797700
    [PubMed - indexed for MEDLINE]

    Related citations

    19.

    The carrier frequency of α-globin gene triplication in an Iranian population with normal or borderline hematological parameters.

    Moosavi SF, Amirian A, Zarbakhsh B, Kordafshari A, Mirzahoseini H, Zeinali S, Karimipoor M.

    Hemoglobin. 2011;35(4):323-30.

    PMID:
    21797699
    [PubMed - indexed for MEDLINE]

    Related citations

    20.

    A novel deletion/insertion caused by a replication error in the β-globin gene locus control region.

    Joly P, Lacan P, Garcia C, Meley R, Pondarré C, Francina A.

    Hemoglobin. 2011;35(4):316-22.

    PMID:
    21797698
    [PubMed - indexed for MEDLINE]

    Related citations

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