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Journal Abstract Search

326 related items for PubMed ID: 25706573

  • 21. Clinical expression of haemochromatosis in Irish C282Y homozygotes identified through family screening.
    Gleeson F, Ryan E, Barrett S, Crowe J.
    Eur J Gastroenterol Hepatol; 2004 Sep; 16(9):859-63. PubMed ID: 15316409
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  • 22. 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
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  • 23. HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.
    Barton JC, Wiener HW, Acton RT, Go RC.
    Blood Cells Mol Dis; 2005 Jun; 34(1):38-47. PubMed ID: 15607698
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  • 24. Genotypic/phenotypic correlations in genetic hemochromatosis: evolution of diagnostic criteria.
    Adams PC, Chakrabarti S.
    Gastroenterology; 1998 Feb; 114(2):319-23. PubMed ID: 9453492
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  • 25. Increased risk of death from iron overload among 422 treated probands with HFE hemochromatosis and serum levels of ferritin greater than 1000 μg/L at diagnosis.
    Barton JC, Barton JC, Acton RT, So J, Chan S, Adams PC.
    Clin Gastroenterol Hepatol; 2012 Apr; 10(4):412-6. PubMed ID: 22265917
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  • 26. Using iron studies to predict HFE mutations in New Zealand: implications for laboratory testing.
    O'Toole R, Romeril K, Bromhead C.
    Intern Med J; 2017 Apr; 47(4):447-454. PubMed ID: 28019068
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  • 27. Testing for haemochromatosis in a liver clinic population: relationship between ethnic origin, HFE gene mutations, liver histology and serum iron markers.
    Moodie SJ, Ang L, Stenner JM, Finlayson C, Khotari A, Levin GE, Maxwell JD.
    Eur J Gastroenterol Hepatol; 2002 Mar; 14(3):223-9. PubMed ID: 11953685
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  • 28. Population screening for hemochromatosis: a study in 5370 Spanish blood donors.
    Sánchez M, Villa M, Ingelmo M, Sanz C, Bruguera M, Ascaso C, Oliva R.
    J Hepatol; 2003 Jun; 38(6):745-50. PubMed ID: 12763366
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  • 29. A population-based study of the clinical expression of the hemochromatosis gene.
    Olynyk JK, Cullen DJ, Aquilia S, Rossi E, Summerville L, Powell LW.
    N Engl J Med; 1999 Sep 02; 341(10):718-24. PubMed ID: 10471457
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  • 31. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes.
    Raddatz D, Legler T, Lynen R, Addicks N, Ramadori G.
    Z Gastroenterol; 2003 Nov 02; 41(11):1069-76. PubMed ID: 14648375
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  • 33. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.
    Lawless MW, White M, Mankan AK, O'Dwyer MJ, Norris S.
    Tissue Antigens; 2007 Oct 02; 70(4):294-300. PubMed ID: 17767550
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  • 34. Relationship of body iron stores to levels of serum ferritin, serum iron, unsaturated iron binding capacity and transferrin saturation in patients with iron storage disease.
    Beutler E, Felitti V, Ho NJ, Gelbart T.
    Acta Haematol; 2002 Oct 02; 107(3):145-9. PubMed ID: 11978935
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  • 36. Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis.
    Del-Castillo-Rueda A, Moreno-Carralero MI, Cuadrado-Grande N, Alvarez-Sala-Walther LA, Enríquez-de-Salamanca R, Méndez M, Morán-Jiménez MJ.
    Gene; 2012 Oct 15; 508(1):15-20. PubMed ID: 22890139
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  • 39. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
    Byrnes V, Ryan E, O'Keane C, Crowe J.
    Blood Cells Mol Dis; 2000 Feb 15; 26(1):2-8. PubMed ID: 10772870
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  • 40. Effect of hemochromatosis genotype and lifestyle factors on iron and red cell indices in a community population.
    Rossi E, Bulsara MK, Olynyk JK, Cullen DJ, Summerville L, Powell LW.
    Clin Chem; 2001 Feb 15; 47(2):202-8. PubMed ID: 11159767
    [Abstract] [Full Text] [Related]

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