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Journal Abstract Search


97 related items for PubMed ID: 17160266

  • 1. HFE gene mutations in Brazilian thalassemic patients.
    Oliveira TM, Souza FP, Jardim AC, Cordeiro JA, Pinho JR, Sitnik R, Estevão IF, Bonini-Domingos CR, Rahal P.
    Braz J Med Biol Res; 2006 Dec; 39(12):1575-80. PubMed ID: 17160266
    [Abstract] [Full Text] [Related]

  • 2. The role of HFE mutations on iron metabolism in beta-thalassemia carriers.
    Martins R, Picanço I, Fonseca A, Ferreira L, Rodrigues O, Coelho M, Seixas T, Miranda A, Nunes B, Costa L, Romão L, Faustino P.
    J Hum Genet; 2004 Dec; 49(12):651-655. PubMed ID: 15538648
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. Heterozygosity for the H63D mutation in the hereditary hemochromatosis (HFE) gene may lead into severe iron overload in beta-thalassemia minor: observations in a thalassemic kindred.
    Ruiz-Argüelles GJ, Garcés-Eisele J, Reyes-Núñez V, Sánchez-Anzaldo J, Ruiz-Delgado GJ, Jiménez-González C, Carrera B.
    Rev Invest Clin; 2001 Apr; 53(2):117-20. PubMed ID: 11421105
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population.
    Leone PE, Giménez P, Collantes JC, Paz-y-Miño C.
    Ann Hematol; 2005 Feb; 84(2):103-5. PubMed ID: 15517265
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. 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]

  • 10. [HFE gene mutations in Tunisian major beta-Thalassemia and iron overload].
    Mellouli F, El Borgi W, Kaabi H, Ben Hassen E, Sassi R, Hmida H, Cherif G, Maamar M, Zouari B, Boukef K, Bejaoui M, Hmida S.
    Transfus Clin Biol; 2006 Dec; 13(6):353-7. PubMed ID: 17303462
    [Abstract] [Full Text] [Related]

  • 11. The influence of hemochromatosis mutations on iron overload of thalassemia major.
    Longo F, Zecchina G, Sbaiz L, Fischer R, Piga A, Camaschella C.
    Haematologica; 1999 Sep; 84(9):799-803. PubMed ID: 10477452
    [Abstract] [Full Text] [Related]

  • 12. Analysis of the HFE gene (C282Y, H63D and S65C) mutations in a general Chinese Han population.
    Lin A, Yan WH, Xu HH, Zhu M, Zhou MY.
    Tissue Antigens; 2007 Sep; 70(3):252-5. PubMed ID: 17661915
    [Abstract] [Full Text] [Related]

  • 13. Mild iron overload in patients carrying the HFE S65C gene mutation: a retrospective study in patients with suspected iron overload and healthy controls.
    Holmström P, Marmur J, Eggertsen G, Gåfvels M, Stål P.
    Gut; 2002 Nov; 51(5):723-30. PubMed ID: 12377814
    [Abstract] [Full Text] [Related]

  • 14. Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain.
    de Diego C, Murga MJ, Martínez-Castro P.
    Genet Test; 2004 Nov; 8(3):263-7. PubMed ID: 15727249
    [Abstract] [Full Text] [Related]

  • 15. [The importance of DNA analysis of C282Y, H63D and S65C mutations in the HFE gene].
    Drastíková M, Beránek M, Hegerová J, Putzová D.
    Cas Lek Cesk; 2012 Nov; 151(9):428-31. PubMed ID: 23102134
    [Abstract] [Full Text] [Related]

  • 16. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
    Spínola C, Brehm A, Spínola H.
    Ann Hematol; 2011 Jan; 90(1):29-32. PubMed ID: 20714725
    [Abstract] [Full Text] [Related]

  • 17. Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain.
    Altes A, Ruiz A, Barceló MJ, Remacha AF, Puig T, Maya AJ, Castell C, Amate JM, Saz Z, Baiget M.
    Genet Test; 2004 Jan; 8(4):407-10. PubMed ID: 15684872
    [Abstract] [Full Text] [Related]

  • 18. Status of HFE mutation in thalassemia syndromes in north India.
    Agarwal S, Tewari D, Arya V, Moorchung N, Tripathi R, Chaudhuri G, Pradhan M.
    Ann Hematol; 2007 Jul; 86(7):483-5. PubMed ID: 17401564
    [Abstract] [Full Text] [Related]

  • 19. Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.
    Milman N, á Steig T, Koefoed P, Pedersen P, Fenger K, Nielsen FC.
    Ann Hematol; 2005 Mar; 84(3):146-9. PubMed ID: 15042317
    [Abstract] [Full Text] [Related]

  • 20. Effect of the Hemochromatosis Mutations on Iron Overload among the Indian β Thalassemia Carriers.
    Nadkarni AH, Singh AA, Colaco S, Hariharan P, Colah RB, Ghosh K.
    J Clin Lab Anal; 2017 May; 31(3):. PubMed ID: 27561698
    [Abstract] [Full Text] [Related]


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