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

PUBMED FOR HANDHELDS

Journal Abstract Search

155 related items for PubMed ID: 14765621

  • 1. Distribution of C282Y and H63D mutations in the HFE gene in healthy Asian Indians and patients with thalassaemia major.
    Kaur G, Rapthap CC, Xavier M, Saxena R, Choudhary VP, Reuben SK, Mehra NK.
    Natl Med J India; 2003; 16(6):309-10. PubMed ID: 14765621
    [Abstract] [Full Text] [Related]

  • 2. Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait.
    Garewal G, Das R, Ahluwalia J, Marwaha RK.
    Eur J Haematol; 2005 Apr; 74(4):333-6. PubMed ID: 15777346
    [Abstract] [Full Text] [Related]

  • 3. Frequency of HFE gene mutations in Iranian beta-thalassaemia minor patients.
    Jazayeri M, Bakayev V, Adibi P, Haghighi Rad F, Zakeri H, Kalantar E, Zali MR.
    Eur J Haematol; 2003 Dec; 71(6):408-11. PubMed ID: 14703689
    [Abstract] [Full Text] [Related]

  • 4. High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy.
    De Marco F, Liguori R, Giardina MG, D'Armiento M, Angelucci E, Lucariello A, Morante R, Cimino L, Galeota-Lanza A, Tarantino G, Ascione A, Budillon G, Vecchione R, Martinelli R, Matarazzo M, De Simone V.
    Clin Chem Lab Med; 2004 Jan; 42(1):17-24. PubMed ID: 15061375
    [Abstract] [Full Text] [Related]

  • 5. S65C and other mutations in the haemochromatosis gene in the Czech population.
    Cimburová M, Půtová I, Provazníková H, Pintérová D, Horák J.
    Folia Biol (Praha); 2005 Jan; 51(6):172-6. PubMed ID: 16419611
    [Abstract] [Full Text] [Related]

  • 6. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
    Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.
    Eur J Immunogenet; 2000 Jun; 27(3):129-34. PubMed ID: 10940080
    [Abstract] [Full Text] [Related]

  • 7. Haemochromatosis in patients with beta-thalassaemia trait.
    Piperno A, Mariani R, Arosio C, Vergani A, Bosio S, Fargion S, Sampietro M, Girelli D, Fraquelli M, Conte D, Fiorelli G, Camaschella C.
    Br J Haematol; 2000 Dec; 111(3):908-14. PubMed ID: 11122155
    [Abstract] [Full Text] [Related]

  • 8. HFE mutations, iron deficiency and overload in 10,500 blood donors.
    Jackson HA, Carter K, Darke C, Guttridge MG, Ravine D, Hutton RD, Napier JA, Worwood M.
    Br J Haematol; 2001 Aug; 114(2):474-84. PubMed ID: 11529872
    [Abstract] [Full Text] [Related]

  • 9. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
    Trifa AP, Popp RA, Militaru MS, Farcaş MF, Crişan TO, Gana I, Cucuianu A, Pop IV.
    J Gastrointestin Liver Dis; 2012 Jun; 21(2):177-80. PubMed ID: 22720307
    [Abstract] [Full Text] [Related]

  • 10. Role of HFE gene mutations on developing iron overload in beta-thalassaemia carriers in Egypt.
    Madani HA, Afify RA, Abd El-Aal AA, Salama N, Ramy N.
    East Mediterr Health J; 2011 Jun; 17(6):546-51. PubMed ID: 21796974
    [Abstract] [Full Text] [Related]

  • 11. Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload.
    Porto G, Cardoso CS, Gordeuk V, Cruz E, Fraga J, Areias J, Oliveira JC, Bravo F, Gangaidzo IT, MacPhail AP, Gomo ZA, Moyo VM, Melo G, Silva C, Justiça B, de Sousa M.
    Eur J Haematol; 2001 Aug; 67(2):110-8. PubMed ID: 11722599
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
    Kucinskas L, Juzenas S, Sventoraityte J, Cedaviciute R, Vitkauskiene A, Kalibatas V, Kondrackiene J, Kupcinskas L.
    Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086
    [Abstract] [Full Text] [Related]

  • 17. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
    Cukjati M, Vaupotic T, Rupreht R, Curin-Serbec V.
    BMC Med Genet; 2007 Nov 23; 8():69. PubMed ID: 18036208
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Haemochromatosis gene mutations in idiopathic dilated cardiomyopathy.
    Mahon NG, Coonar AS, Jeffery S, Coccolo F, Akiyu J, Zal B, Houlston R, Levin GE, Baboonian C, McKenna WJ.
    Heart; 2000 Nov 23; 84(5):541-7. PubMed ID: 11040018
    [Abstract] [Full Text] [Related]

  • 20. Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis.
    Bittencourt PL, Marin ML, Couto CA, Cançado EL, Carrilho FJ, Goldberg AC.
    Clinics (Sao Paulo); 2009 Nov 23; 64(9):837-41. PubMed ID: 19759876
    [Abstract] [Full Text] [Related]

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