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Journal Abstract Search

275 related items for PubMed ID: 26633544

  • 21.
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  • 22. Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis.
    Bittencourt PL, Marin ML, Couto CA, Cançado EL, Carrilho FJ, Goldberg AC.
    Clinics (Sao Paulo); 2009; 64(9):837-41. PubMed ID: 19759876
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  • 25. Non-HFE hepatic iron overload.
    Pietrangelo A, Caleffi A, Corradini E.
    Semin Liver Dis; 2011 Aug; 31(3):302-18. PubMed ID: 21901660
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  • 26. The molecular pathogenesis of hereditary hemochromatosis.
    Babitt JL, Lin HY.
    Semin Liver Dis; 2011 Aug; 31(3):280-92. PubMed ID: 21901658
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  • 28. Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
    Santos PCJL, Krieger JE, Pereira AC.
    Int J Mol Sci; 2012 Aug; 13(2):1497-1511. PubMed ID: 22408404
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  • 30. [Pathophysiology and genetics of classic HFE (type 1) hemochromatosis].
    Loréal O, Ropert M, Mosser A, Déhais V, Deugnier Y, David V, Brissot P, Jouanolle AM.
    Presse Med; 2007 Sep; 36(9 Pt 2):1271-7. PubMed ID: 17521857
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  • 32. Disruption of hemochromatosis protein and transferrin receptor 2 causes iron-induced liver injury in mice.
    Delima RD, Chua AC, Tirnitz-Parker JE, Gan EK, Croft KD, Graham RM, Olynyk JK, Trinder D.
    Hepatology; 2012 Aug; 56(2):585-93. PubMed ID: 22383097
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  • 33.
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  • 34. Clinicopathological study of Japanese patients with genetic iron overload syndromes.
    Hattori A, Miyajima H, Tomosugi N, Tatsumi Y, Hayashi H, Wakusawa S.
    Pathol Int; 2012 Sep; 62(9):612-8. PubMed ID: 22924847
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  • 35. Assessment of iron overload in a cohort of Sri Lankan patients with transfusion dependent beta thalassaemia and its correlation with pathogenic variants in HBB, HFE, SLC40A1, and TFR2 genes.
    Dissanayake R, Samarasinghe N, Waidyanatha S, Pathirana S, Neththikumara N, Dissanayake VHW, Wetthasinghe K, Gooneratne L, Wickramasinghe P.
    BMC Pediatr; 2022 Jun 15; 22(1):344. PubMed ID: 35705926
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  • 36.
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  • 37. Iron stores modulate hepatic hepcidin expression by an HFE-independent pathway.
    Gehrke SG, Herrmann T, Kulaksiz H, Merle U, Bents K, Kaiser I, Riedel HD, Stremmel W.
    Digestion; 2005 Jun 15; 72(1):25-32. PubMed ID: 16103673
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  • 40. Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians.
    Dhillon BK, Chopra G, Jamwal M, Chandak GR, Duseja A, Malhotra P, Chawla YK, Garewal G, Das R.
    Blood Cells Mol Dis; 2018 Nov 15; 73():14-21. PubMed ID: 30195625
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