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Journal Abstract Search

336 related items for PubMed ID: 11518736

  • 21.
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  • 22. Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features.
    Sham RL, Phatak PD, West C, Lee P, Andrews C, Beutler E.
    Blood Cells Mol Dis; 2005; 34(2):157-61. PubMed ID: 15727899
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  • 23. Genetics of hemochromatosis.
    Cullen LM, Anderson GJ, Ramm GA, Jazwinska EC, Powell LW.
    Annu Rev Med; 1999; 50():87-98. PubMed ID: 10073265
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  • 24. Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.
    Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT.
    Blood Cells Mol Dis; 1999; 25(3-4):147-55. PubMed ID: 10575540
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  • 29. Transferrin receptor 2 (TfR2) and HFE mutational analysis in non-C282Y iron overload: identification of a novel TfR2 mutation.
    Mattman A, Huntsman D, Lockitch G, Langlois S, Buskard N, Ralston D, Butterfield Y, Rodrigues P, Jones S, Porto G, Marra M, De Sousa M, Vatcher G.
    Blood; 2002 Aug 01; 100(3):1075-7. PubMed ID: 12130528
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  • 30. Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.
    Wrede CE, Hutzler S, Bollheimer LC, Buettner R, Hellerbrand C, Schöelmerich J, Palitzsch KD.
    Isr Med Assoc J; 2004 Jan 01; 6(1):30-3. PubMed ID: 14740507
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  • 31. 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 Jan 01; 27(1):290-3. PubMed ID: 11358390
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  • 32. The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients.
    Politou M, Kalotychou V, Pissia M, Rombos Y, Sakellaropoulos N, Papanikolaou G.
    Haematologica; 2004 Apr 01; 89(4):490-2. PubMed ID: 15075083
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  • 33.
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  • 34. Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis.
    Wallace DF, Pedersen P, Dixon JL, Stephenson P, Searle JW, Powell LW, Subramaniam VN.
    Blood; 2002 Jul 15; 100(2):692-4. PubMed ID: 12091366
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  • 36. Hemochromatosis: genetics and pathophysiology.
    Beutler E.
    Annu Rev Med; 2006 Jul 15; 57():331-47. PubMed ID: 16409153
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  • 38. Hereditary hemochromatosis--a new look at an old disease.
    Pietrangelo A.
    N Engl J Med; 2004 Jun 03; 350(23):2383-97. PubMed ID: 15175440
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