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Journal Abstract Search

209 related items for PubMed ID: 30166352

  • 21.
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  • 22. The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype.
    Le Gac G, Scotet V, Ka C, Gourlaouen I, Bryckaert L, Jacolot S, Mura C, Férec C.
    Hum Mol Genet; 2004 Sep 01; 13(17):1913-8. PubMed ID: 15254010
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  • 23. 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 Sep 01; 72(1):25-32. PubMed ID: 16103673
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  • 28. Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes.
    Mendes AI, Ferro A, Martins R, Picanço I, Gomes S, Cerqueira R, Correia M, Nunes AR, Esteves J, Fleming R, Faustino P.
    Ann Hematol; 2009 Mar 01; 88(3):229-34. PubMed ID: 18762941
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  • 30. Recent advances in understanding haemochromatosis: a transition state.
    Robson KJ, Merryweather-Clarke AT, Cadet E, Viprakasit V, Zaahl MG, Pointon JJ, Weatherall DJ, Rochette J.
    J Med Genet; 2004 Oct 01; 41(10):721-30. PubMed ID: 15466004
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  • 33. HFE and Non-HFE Hereditary Hemochromatosis Based on Screening of 854 Individuals: 12 Years of an Iranian Experience.
    Zarifian Yeganeh R, Akbari Kelishomi M, Ahmadpour Jenaghard A, Salmani B, Vahidi Z, Makvand M, Azad M, Kooshki M, Bouraqi Y, Azarkeivan A, Najmabadi H, Neishabury M.
    Genet Test Mol Biomarkers; 2024 Jul 01; 28(7):289-296. PubMed ID: 38980801
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  • 34. 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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  • 36. Juvenile hemochromatosis associated with heterozygosity for novel hemojuvelin mutations and with unknown cofactors.
    Pelusi S, Rametta R, Della Corte C, Congia R, Dongiovanni P, Pulixi EA, Fargion S, Fracanzani AL, Nobili V, Valenti L.
    Ann Hepatol; 2014 Oct 15; 13(5):568-71. PubMed ID: 25152992
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  • 38. [Hereditary and acquired iron overload].
    de Korwin JD.
    Nephrol Ther; 2006 Nov 15; 2 Suppl 5():S304-12. PubMed ID: 17373275
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  • 39. Hemochromatosis in India: First Report of Whole Exome Sequencing With Review of the Literature.
    Koshy A, Mukkada RJ, Chettupuzha AP, Francis JV, Kandathil JC, Mahadevan P.
    J Clin Exp Hepatol; 2020 Nov 15; 10(2):163-169. PubMed ID: 32189932
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