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Journal Abstract Search

248 related items for PubMed ID: 19822954

  • 21. [Mutations in the HFE gene (C282Y, H63D, S65C) in alcoholic patients with finding of iron overload].
    Campos Franco J, González Quintela A, Fernández de Trocóniz LL, Barros Angueira F, Pérez-Quintela BV, Pérez Becerra E, Martínez de Rituerto ST, Otero Antón E, Torre Carballada JA.
    Rev Clin Esp; 2002 Oct; 202(10):534-9. PubMed ID: 12361551
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  • 26. Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain.
    Aranda N, Viteri FE, Montserrat C, Arija V.
    Ann Hematol; 2010 Aug; 89(8):767-73. PubMed ID: 20107990
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  • 27. Analysis of HFE genes C282Y, H63D, and S65D in patients with hyperferritinemia from northeastern Brazil.
    Leão GD, Freire JM, Cunha Fernandes AL, Moura de Oliveira TM, Leão ND, Gil EA, de Vasconcelos RC, Azevedo JP, de Farias Sales VS, de Araújo Moura Lemos TM, Leão MD, do Nascimento FF, Maciel JF, de Freitas RV, de Souza Paiva A, Cavalcanti GB.
    J Clin Lab Anal; 2014 May; 28(3):178-85. PubMed ID: 24395214
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  • 31. 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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  • 32. Genetic hemochromatosis, a Celtic disease: is it now time for population screening?
    Byrnes V, Ryan E, Barrett S, Kenny P, Mayne P, Crowe J.
    Genet Test; 2001 Jun; 5(2):127-30. PubMed ID: 11551098
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  • 33. HFE gene mutations in patients with alcoholic liver disease. A prospective study from northwestern Poland.
    Raszeja-Wyszomirska J, Kurzawski G, Zawada I, Suchy J, Lubinski J, Milkiewicz P.
    Pol Arch Med Wewn; 2010 Apr; 120(4):127-31. PubMed ID: 20424537
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  • 34. Analysis of haemochromatosis gene mutations in a population from the Mediterranean Basin.
    Campo S, Restuccia T, Villari D, Raffa G, Cucinotta D, Squadrito G, Pollicino T, Raimondo G.
    Liver; 2001 Aug; 21(4):233-6. PubMed ID: 11454185
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  • 35. Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.
    Hellerbrand C, Bosserhoff AK, Seegers S, Lingner G, Wrede C, Lock G, Schölmerich J, Büttner R.
    Scand J Gastroenterol; 2001 Nov; 36(11):1211-6. PubMed ID: 11686223
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  • 36. Hemochromatosis (HFE) gene mutations in Brazilian chronic hemodialysis patients.
    Perícole FV, Alves MA, Saad ST, Costa FF.
    Braz J Med Biol Res; 2005 Sep; 38(9):1321-4. PubMed ID: 16138214
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  • 37. HFE mutations, iron deficiency and overload in 10,500 blood donors.
    Jackson HA, Carter K, Darke C, Guttridge MG, Ravine D, Hutton RD, Napier JA, Worwood M.
    Br J Haematol; 2001 Aug; 114(2):474-84. PubMed ID: 11529872
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  • 38. Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathy.
    Hannuksela J, Leppilampi M, Peuhkurinen K, Kärkkäinen S, Saastamoinen E, Heliö T, Kaartinen M, Nieminen MS, Nieminen P, Parkkila S.
    Eur J Heart Fail; 2005 Jan; 7(1):103-8. PubMed ID: 15642540
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  • 39. A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote.
    Wallace DF, Dooley JS, Walker AP.
    Gastroenterology; 1999 Jun; 116(6):1409-12. PubMed ID: 10348824
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  • 40. 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 Jun; 27(1):290-3. PubMed ID: 11358390
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