These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


160 related items for PubMed ID: 15768554

  • 61.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 62.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 63. A report of 8 cases with hemoglobin H disease in an Iranian family.
    Azarkeivan A, Neishabury M, Hadavi V, Esteghamat F, Enrahimkhani S, Najmabadi H.
    Pediatr Hematol Oncol; 2010 Aug; 27(5):405-12. PubMed ID: 20670167
    [Abstract] [Full Text] [Related]

  • 64.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 65.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 66.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 67. Molecular and hematologic analysis of hemoglobin Q-Iran and hemoglobin Setif in Iranian families.
    Rahimi Z, Rezaei M, L Nagel R, Muniz A.
    Arch Iran Med; 2008 Jul; 11(4):382-6. PubMed ID: 18588369
    [Abstract] [Full Text] [Related]

  • 68. Dominantly Inherited beta-Thalassemia.
    Efremov GD.
    Hemoglobin; 2007 Jul; 31(2):193-207. PubMed ID: 17486503
    [Abstract] [Full Text] [Related]

  • 69.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 70.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 71.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 72.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 73.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 74. Molecular spectrum of beta-thalassemia mutations in Northwestern Iran.
    Hosseinpour Feizi MA, Hosseinpour Feizi AA, Pouladi N, Haghi M, Azarfam P.
    Hemoglobin; 2008 Jul; 32(3):255-61. PubMed ID: 18473241
    [Abstract] [Full Text] [Related]

  • 75. A multicenter trial of the effectiveness of zeta-globin enzyme-linked immunosorbent assay and hemoglobin H inclusion body screening for the detection of alpha0-thalassemia trait.
    Lafferty JD, Barth DS, Sheridan BL, McFarlane AG, Halchuk LM, Raby A, Crowther MA.
    Am J Clin Pathol; 2008 Feb; 129(2):309-15. PubMed ID: 18208812
    [Abstract] [Full Text] [Related]

  • 76.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 77. The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H disease.
    Orkin SH, Old J, Lazarus H, Altay C, Gurgey A, Weatherall DJ, Nathan DG.
    Cell; 1979 May; 17(1):33-42. PubMed ID: 455460
    [Abstract] [Full Text] [Related]

  • 78. 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 May; 31(4):439-52. PubMed ID: 17994378
    [Abstract] [Full Text] [Related]

  • 79.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 80. Heterozygous Hb Hope [beta136(H14)Gly --> Asp] in association with heterozygous beta0-thalassemia with apparent homozygous expression, in a Spanish patient.
    Beneitez D, Carrera A, Duran-Suárez JR, Paz V, León A, García Talavera J.
    Hemoglobin; 2006 May; 30(1):45-9. PubMed ID: 16540415
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 8.