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Journal Abstract Search

110 related items for PubMed ID: 10756357

  • 1. Immunohistochemistry of HFE in the duodenum of C282Y homozygotes with antisera for recombinant HFE protein.
    Zuccon L, Corsi B, Levi S, Mattioli M, Fracanzani AL, Corti A, Albertini A, Sampietro M, Fargion S, Arosio P.
    Haematologica; 2000 Apr; 85(4):346-51. PubMed ID: 10756357
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  • 2. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
    Byrnes V, Ryan E, O'Keane C, Crowe J.
    Blood Cells Mol Dis; 2000 Feb; 26(1):2-8. PubMed ID: 10772870
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  • 3. 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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  • 4. Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.
    Bittencourt PL, Palácios SA, Couto CA, Cançado EL, Carrilho FJ, Laudanna AA, Kalil J, Gayotto LC, Goldberg AC.
    Braz J Med Biol Res; 2002 Mar; 35(3):329-35. PubMed ID: 11887210
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  • 5. 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 Mar; 27(1):290-3. PubMed ID: 11358390
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  • 6. Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis.
    Parkkila S, Waheed A, Britton RS, Bacon BR, Zhou XY, Tomatsu S, Fleming RE, Sly WS.
    Proc Natl Acad Sci U S A; 1997 Nov 25; 94(24):13198-202. PubMed ID: 9371823
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  • 7. HFE based re-evaluation of heterozygous hemochromatosis.
    Moirand R, Guyader D, Mendler MH, Jouanolle AM, Le Gall JY, David V, Brissot P, Deugnier Y.
    Am J Med Genet; 2002 Sep 01; 111(4):356-61. PubMed ID: 12210292
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  • 8. Differential HFE allele expression in hemochromatosis heterozygotes.
    Rosmorduc O, Poupon R, Nion I, Wendum D, Feder J, Béréziat G, Hermelin B.
    Gastroenterology; 2000 Oct 01; 119(4):1075-86. PubMed ID: 11040194
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  • 13. Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives.
    Moirand R, Jouanolle AM, Brissot P, Le Gall JY, David V, Deugnier Y.
    Gastroenterology; 1999 Feb 01; 116(2):372-7. PubMed ID: 9922318
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  • 14. Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum.
    Waheed A, Parkkila S, Saarnio J, Fleming RE, Zhou XY, Tomatsu S, Britton RS, Bacon BR, Sly WS.
    Proc Natl Acad Sci U S A; 1999 Feb 16; 96(4):1579-84. PubMed ID: 9990067
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  • 16. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL, Ou CY, Cappuccio J, Braggins C, Dunnigan K, Phatak PD.
    Blood Cells Mol Dis; 1997 Aug 16; 23(2):314-20. PubMed ID: 9410475
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  • 18. HFE gene mutation (C282Y) and phenotypic expression among a hospitalised population in a high prevalence area of haemochromatosis.
    Distante S, Berg JP, Lande K, Haug E, Bell H.
    Gut; 2000 Oct 16; 47(4):575-9. PubMed ID: 10986220
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  • 20. Hepatic iron overload: direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis.
    Press RD, Flora K, Gross C, Rabkin JM, Corless CL.
    Am J Clin Pathol; 1998 May 16; 109(5):577-84. PubMed ID: 9576576
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