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1113 related items for PubMed ID: 10772870

  • 21. HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.
    Barton JC, Wiener HW, Acton RT, Go RC.
    Blood Cells Mol Dis; 2005; 34(1):38-47. PubMed ID: 15607698
    [Abstract] [Full Text] [Related]

  • 22. 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; 116(2):372-7. PubMed ID: 9922318
    [Abstract] [Full Text] [Related]

  • 23. Iron-overload-related disease in HFE hereditary hemochromatosis.
    Allen KJ, Gurrin LC, Constantine CC, Osborne NJ, Delatycki MB, Nicoll AJ, McLaren CE, Bahlo M, Nisselle AE, Vulpe CD, Anderson GJ, Southey MC, Giles GG, English DR, Hopper JL, Olynyk JK, Powell LW, Gertig DM.
    N Engl J Med; 2008 Jan 17; 358(3):221-30. PubMed ID: 18199861
    [Abstract] [Full Text] [Related]

  • 24. Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestry.
    Beutler E, Felitti V, Gelbart T, Waalen J.
    Br J Haematol; 2003 Mar 17; 120(5):887-93. PubMed ID: 12614226
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. A common intron 3 mutation (IVS3 -48c-->g) leads to misdiagnosis of the c.845G-->A (C282Y) HFE gene mutation.
    Beutler E, Gelbart T.
    Blood Cells Mol Dis; 2000 Jun 01; 26(3):229-33. PubMed ID: 10950943
    [Abstract] [Full Text] [Related]

  • 27. The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic.
    Beutler E, Felitti V, Gelbart T, Ho N.
    Ann Intern Med; 2000 Sep 05; 133(5):329-37. PubMed ID: 10979877
    [Abstract] [Full Text] [Related]

  • 28. Screening for iron overload in the Turkish population.
    Barut G, Balci H, Bozdayi M, Hatemi I, Ozcelik D, Senturk H.
    Dig Dis; 2003 Sep 05; 21(3):279-85. PubMed ID: 14571105
    [Abstract] [Full Text] [Related]

  • 29. Increased duodenal DMT-1 expression and unchanged HFE mRNA levels in HFE-associated hereditary hemochromatosis and iron deficiency.
    Byrnes V, Barrett S, Ryan E, Kelleher T, O'Keane C, Coughlan B, Crowe J.
    Blood Cells Mol Dis; 2002 Sep 05; 29(3):251-60. PubMed ID: 12547214
    [Abstract] [Full Text] [Related]

  • 30. 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 05; 35(3):329-35. PubMed ID: 11887210
    [Abstract] [Full Text] [Related]

  • 31. Hereditary hemochromatosis in north-eastern Romania.
    Voicu PM, Cojocariu C, Petrescu-Dănilă E, Stanciu C, Covic M, Rusu M, Trifan A.
    Rev Med Chir Soc Med Nat Iasi; 2010 Mar 05; 114(4):982-7. PubMed ID: 21495455
    [Abstract] [Full Text] [Related]

  • 32. Differential HFE allele expression in hemochromatosis heterozygotes.
    Rosmorduc O, Poupon R, Nion I, Wendum D, Feder J, Béréziat G, Hermelin B.
    Gastroenterology; 2000 Oct 05; 119(4):1075-86. PubMed ID: 11040194
    [Abstract] [Full Text] [Related]

  • 33. Testing for haemochromatosis in a liver clinic population: relationship between ethnic origin, HFE gene mutations, liver histology and serum iron markers.
    Moodie SJ, Ang L, Stenner JM, Finlayson C, Khotari A, Levin GE, Maxwell JD.
    Eur J Gastroenterol Hepatol; 2002 Mar 05; 14(3):223-9. PubMed ID: 11953685
    [Abstract] [Full Text] [Related]

  • 34. Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy.
    Cassanelli S, Pignatti E, Montosi G, Garuti C, Mariano M, Campioli D, Carbonieri A, Baldini E, Pietrangelo A.
    J Hepatol; 2001 Apr 05; 34(4):523-8. PubMed ID: 11394651
    [Abstract] [Full Text] [Related]

  • 35. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
    Martinelli AL, Filho R, Cruz S, Franco R, Tavella M, Secaf M, Ramalho L, Zucoloto S, Rodrigues S, Zago M.
    Genet Mol Res; 2005 Mar 31; 4(1):31-8. PubMed ID: 15841433
    [Abstract] [Full Text] [Related]

  • 36. 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 31; 85(4):346-51. PubMed ID: 10756357
    [Abstract] [Full Text] [Related]

  • 37. Individuals homozygous for the H63D mutation have significantly elevated iron indexes.
    Samarasena J, Winsor W, Lush R, Duggan P, Xie Y, Borgaonkar M.
    Dig Dis Sci; 2006 Apr 31; 51(4):803-7. PubMed ID: 16615007
    [Abstract] [Full Text] [Related]

  • 38. HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L.
    Adams PC, McLaren CE, Speechley M, McLaren GD, Barton JC, Eckfeldt JH.
    Can J Gastroenterol; 2013 Jul 31; 27(7):390-2. PubMed ID: 23862168
    [Abstract] [Full Text] [Related]

  • 39. The hepcidin gene promoter nc.-1010C > T; -582A > G haplotype modulates serum ferritin in individuals carrying the common H63D mutation in HFE gene.
    Silva B, Pita L, Gomes S, Gonçalves J, Faustino P.
    Ann Hematol; 2014 Dec 31; 93(12):2063-6. PubMed ID: 25015054
    [Abstract] [Full Text] [Related]

  • 40. The Study of HFE Genotypes and Its Expression Effect on Iron Status of Iranian Haemochromatosis, Iron Deficiency Anemia Patients, Iron-Taker and Non Iron-Taker Controls.
    Beiranvand E, Abediankenari S, Rostamian M, Beiranvand B, Naazeri S.
    Recent Adv DNA Gene Seq; 2015 Dec 31; 9(1):58-64. PubMed ID: 25687342
    [Abstract] [Full Text] [Related]

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