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Journal Abstract Search

211 related items for PubMed ID: 15777346

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  • 3. 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
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  • 5. Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder.
    Viprakasit V, Vathesathokit P, Chinchang W, Tachavanich K, Pung-Amritt P, Wimhurst VL, Yenchitsomanus PT, Merryweather-Clarke AT, Tanphaichitr VS.
    Eur J Haematol; 2004 Jul; 73(1):43-9. PubMed ID: 15182337
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  • 6. 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
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  • 7. 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
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  • 9. 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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  • 10. Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian population.
    Sassi R, Hmida S, Kaabi H, Hajjej A, Abid A, Abdelkefi S, Yacoub S, Maamar M, Mojaat N, Ben Hamed L, Bellali H, Dridi A, Jridi A, Midouni B, Boukef MK.
    Ann Genet; 2004 Mar; 47(4):325-30. PubMed ID: 15581829
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  • 11. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
    Nie L, Ai XF, Zheng YZ, Li QH, Yang L, Xiao ZJ.
    Zhonghua Xue Ye Xue Za Zhi; 2009 Apr; 30(4):223-8. PubMed ID: 19731820
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  • 12. 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 Apr; 49(12):651-655. PubMed ID: 15538648
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  • 15. Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan.
    Sharif Y, Irshad S, Tariq A, Rasheed S, Tariq MH.
    Saudi Med J; 2019 Sep; 40(9):887-892. PubMed ID: 31522215
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  • 16. 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
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  • 17. 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 Dec; 16(6):309-10. PubMed ID: 14765621
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  • 18. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
    Aguilar-Martinez P, Esculié-Coste C, Bismuth M, Giansily-Blaizot M, Larrey D, Schved JF.
    Blood Cells Mol Dis; 2001 Dec; 27(1):290-3. PubMed ID: 11358390
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  • 19. Frequency and clinical expression of HFE gene mutations in a Spanish population of subjects with abnormal iron metabolism.
    Gómez-Llorente C, Miranda-León MT, Blanco S, Gandia-Pla S, Gómez-Capilla JA, Fárez-Vidal ME.
    Ann Hematol; 2005 Oct; 84(10):650-5. PubMed ID: 15986199
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  • 20. [Mutations in the HFE gene (C282Y, H63D, S65C) in alcoholic patients with finding of iron overload].
    Campos Franco J, González Quintela A, Fernández de Trocóniz LL, Barros Angueira F, Pérez-Quintela BV, Pérez Becerra E, Martínez de Rituerto ST, Otero Antón E, Torre Carballada JA.
    Rev Clin Esp; 2002 Oct; 202(10):534-9. PubMed ID: 12361551
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