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Journal Abstract Search

229 related items for PubMed ID: 35668470

  • 21. 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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  • 22. Pathogenesis of hereditary hemochromatosis: genetics and beyond.
    Britton RS, Fleming RE, Parkkila S, Waheed A, Sly WS, Bacon BR.
    Semin Gastrointest Dis; 2002 Apr; 13(2):68-79. PubMed ID: 12064862
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  • 23. Identification of new mutations of the HFE, hepcidin, and transferrin receptor 2 genes by denaturing HPLC analysis of individuals with biochemical indications of iron overload.
    Biasiotto G, Belloli S, Ruggeri G, Zanella I, Gerardi G, Corrado M, Gobbi E, Albertini A, Arosio P.
    Clin Chem; 2003 Dec; 49(12):1981-8. PubMed ID: 14633868
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  • 24. Increased capacity of lymphocytes from hereditary hemochromatosis patients homozygous for the C282Y HFE mutation to respond to the genotoxic effect of diepoxybutane.
    Porto B, Vieira R, Porto G.
    Mutat Res; 2009 Feb 19; 673(1):37-42. PubMed ID: 19146986
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  • 25. 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 19; 28(7):289-296. PubMed ID: 38980801
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  • 26. HFE and non-HFE hemochromatosis.
    Anderson GJ, Powell LW.
    Int J Hematol; 2002 Oct 19; 76(3):203-7. PubMed ID: 12416729
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  • 27. [Iron overload disease: recent findings].
    Licata A, Brucato V, Di Marco V, Barbaria F, Craxì A.
    Ann Ital Med Int; 2004 Oct 19; 19(3):145-54. PubMed ID: 15529941
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  • 28. Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene.
    Altès A, Bach V, Ruiz A, Esteve A, Felez J, Remacha AF, Sardà MP, Baiget M.
    Ann Hematol; 2009 Oct 19; 88(10):951-5. PubMed ID: 19214511
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  • 29. 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 Oct 19; 27(1):290-3. PubMed ID: 11358390
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  • 36. Carriers of the Complex Allele HFE c.[187C>G;340+4T>C] Have Increased Risk of Iron Overload in São Miguel Island Population (Azores, Portugal).
    Branco CC, Gomes CT, De Fez L, Bulhões S, Brilhante MJ, Pereirinha T, Cabral R, Rego AC, Fraga C, Miguel AG, Brasil G, Macedo P, Mota-Vieira L.
    PLoS One; 2015 Oct 19; 10(10):e0140228. PubMed ID: 26501199
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  • 37. Identification of novel mutations in HFE, HFE2, TfR2, and SLC40A1 genes in Chinese patients affected by hereditary hemochromatosis.
    Wang Y, Du Y, Liu G, Guo S, Hou B, Jiang X, Han B, Chang Y, Nie G.
    Int J Hematol; 2017 Apr 19; 105(4):521-525. PubMed ID: 27896572
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  • 39. Iron overload and HFE gene mutations in Polish patients with liver cirrhosis.
    Sikorska K, Romanowski T, Stalke P, Iżycka-Świeszewska E, Bielawski KP.
    Hepatobiliary Pancreat Dis Int; 2011 Jun 19; 10(3):270-5. PubMed ID: 21669570
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