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Journal Abstract Search

310 related items for PubMed ID: 19907151

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  • 3. 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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  • 4. Hereditary iron overload: update on pathophysiology, diagnosis, and treatment.
    Franchini M.
    Am J Hematol; 2006 Mar 15; 81(3):202-9. PubMed ID: 16493621
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  • 12. [Hereditary hemochromatosis].
    Niederau C.
    Internist (Berl); 2003 Feb 15; 44(2):191-205; quiz 206-7. PubMed ID: 12674739
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  • 14. Iron disorders of genetic origin: a changing world.
    Brissot P, Bardou-Jacquet E, Jouanolle AM, Loréal O.
    Trends Mol Med; 2011 Dec 15; 17(12):707-13. PubMed ID: 21862411
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  • 15. Autosomal dominant hereditary hemochromatosis associated with two novel Ferroportin 1 mutations in Spain.
    Bach V, Remacha A, Altés A, Barceló MJ, Molina MA, Baiget M.
    Blood Cells Mol Dis; 2006 Dec 15; 36(1):41-5. PubMed ID: 16257244
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  • 16. Genetic haemochromatosis: genes and mutations associated with iron loading.
    Camaschella C, Roetto A, De Gobbi M.
    Best Pract Res Clin Haematol; 2002 Jun 15; 15(2):261-76. PubMed ID: 12401307
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  • 20. New insights into iron homeostasis through the study of non-HFE hereditary haemochromatosis.
    Roetto A, Camaschella C.
    Best Pract Res Clin Haematol; 2005 Jun 15; 18(2):235-50. PubMed ID: 15737887
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