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Journal Abstract Search

161 related items for PubMed ID: 27561698

  • 1. 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
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  • 2. H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.
    Melis MA, Cau M, Deidda F, Barella S, Cao A, Galanello R.
    Haematologica; 2002 Mar; 87(3):242-5. PubMed ID: 11869934
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  • 3. Investigation of correlation between H63D and C282Y mutations in HFE gene and serum Ferritin level in beta-thalassemia major patients.
    Rahmani R, Naseri P, Safaroghli-Azar A, Tarighi S, Hosseini T, Hojjati MT.
    Transfus Clin Biol; 2019 Nov; 26(4):249-252. PubMed ID: 31679808
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  • 6. 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
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  • 8. 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
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  • 11. 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
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  • 13. Significance of H63D homozygosity in a Basque population with hemochromatosis.
    Castiella A, Zapata E, de Juan MD, Otazua P, Fernandez J, Zubiaurre L, Arriola JA, Gipuzkoa Hemochromatosis Group.
    J Gastroenterol Hepatol; 2010 Jul; 25(7):1295-8. PubMed ID: 20594259
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  • 14. Association of HFE Gene Mutations With Serum Ferritin Level and Heart and Liver Iron Overload in Patients With Transfusion-dependent Beta-Thalassemia.
    Zekavat OR, Zareian Jahromi M, Haghpanah S, Kargar Jahromi Z, Cohan N.
    J Pediatr Hematol Oncol; 2021 Jan; 43(1):e26-e28. PubMed ID: 32925401
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  • 15. Determination of mutations in iron regulating genes of beta thalassemia major patients of Khyber Pakhtunkhwa, Pakistan.
    Shah M, Danish L, Khan NU, Zaman F, Ismail M, Hussain M, Pervaiz R, Iqbal A.
    Mol Genet Genomic Med; 2020 Sep; 8(9):e1310. PubMed ID: 32588561
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  • 16. Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain.
    Aranda N, Viteri FE, Montserrat C, Arija V.
    Ann Hematol; 2010 Aug; 89(8):767-73. PubMed ID: 20107990
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  • 17. Screening for iron overload in the Turkish population.
    Barut G, Balci H, Bozdayi M, Hatemi I, Ozcelik D, Senturk H.
    Dig Dis; 2003 Aug; 21(3):279-85. PubMed ID: 14571105
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  • 18. HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women.
    Warne CD, Zaloumis SG, Bertalli NA, Delatycki MB, Nicoll AJ, McLaren CE, Hopper JL, Giles GG, Anderson GJ, Olynyk JK, Powell LW, Allen KJ, Gurrin LC, HealthIron Study Investigators.
    J Gastroenterol Hepatol; 2017 Apr; 32(4):797-802. PubMed ID: 27784128
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  • 19. [Role of the hemochromatosis gene in prophyria cutanea tarda. Prospective study of 56 cases].
    Skowron F, Bérard F, Grézard P, Wolf F, Morel Y, Perrot H.
    Ann Dermatol Venereol; 2001 May; 128(5):600-4. PubMed ID: 11427792
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