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Journal Abstract Search

262 related items for PubMed ID: 8896550

  • 21. Frequency of the C282Y mutation of hemochromatosis in five French populations.
    Mercier G, Bathelier C, Lucotte G.
    Blood Cells Mol Dis; 1998 Jun; 24(2):165-6. PubMed ID: 9642097
    [Abstract] [Full Text] [Related]

  • 22. Differential HFE allele expression in hemochromatosis heterozygotes.
    Bergamaschi G, Rolandi V, Cazzola M.
    Gastroenterology; 2001 Apr; 120(5):1308-9. PubMed ID: 11288747
    [No Abstract] [Full Text] [Related]

  • 23. An association between the common hereditary hemochromatosis mutation and the factor V Leiden allele in a population with thrombosis.
    Xie YG, Lillicrap DP, Taylor SA.
    Blood; 1998 Aug 15; 92(4):1461-2. PubMed ID: 9694741
    [No Abstract] [Full Text] [Related]

  • 24. The significance of the 187G (H63D) mutation in hemochromatosis.
    Beutler E.
    Am J Hum Genet; 1997 Sep 15; 61(3):762-4. PubMed ID: 9326341
    [No Abstract] [Full Text] [Related]

  • 25. Haemochromatosis gene C282Y homozygotes in an elderly male population.
    Willis G, Wimperis JZ, Smith KC, Fellows IW, Jennings BA.
    Lancet; 1999 Jul 17; 354(9174):221-2. PubMed ID: 10421310
    [Abstract] [Full Text] [Related]

  • 26. Haemochromatosis gene mutation in hepatocellular cancer.
    Willis G, Wimperis JZ, Lonsdale R, Jennings BA.
    Lancet; 1997 Aug 23; 350(9077):565-6. PubMed ID: 9284787
    [No Abstract] [Full Text] [Related]

  • 27. [The molecular genetics of hematochromatosis].
    Rosmorduc O, Hermelin B, Poupon R.
    Gastroenterol Clin Biol; 2002 Aug 23; 26(6-7):563-9. PubMed ID: 12193854
    [No Abstract] [Full Text] [Related]

  • 28. Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis.
    Datz C, Lalloz MR, Vogel W, Graziadei I, Hackl F, Vautier G, Layton DM, Maier-Dobersberger T, Ferenci P, Penner E, Sandhofer F, Bomford A, Paulweber B.
    J Hepatol; 1997 Nov 23; 27(5):773-9. PubMed ID: 9382962
    [Abstract] [Full Text] [Related]

  • 29. The hemochromatosis gene.
    Leber BF.
    Clin Invest Med; 2000 Dec 23; 23(6):382-6. PubMed ID: 11152407
    [No Abstract] [Full Text] [Related]

  • 30. Two novel polymorphisms (E277K and V212V) in the haemochromatosis gene HFE.
    Bradbury R, Fagan E, Payne SJ.
    Hum Mutat; 2000 Jan 23; 15(1):120. PubMed ID: 10612845
    [No Abstract] [Full Text] [Related]

  • 31. Haemochromatosis: strike while the iron is hot.
    Cox T.
    Nat Genet; 1996 Aug 23; 13(4):386-8. PubMed ID: 8696327
    [No Abstract] [Full Text] [Related]

  • 32. Incorrect diagnosis of hereditary hemochromatosis.
    Mirochnik O, Halim-Kertanegara N, Hertzberg M, McDonald D, Liddle C.
    Am J Hematol; 2000 Feb 23; 63(2):104-5. PubMed ID: 10629581
    [No Abstract] [Full Text] [Related]

  • 33. A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern England.
    Willis G, Jennings BA, Goodman E, Fellows IW, Wimperis JZ.
    Blood Cells Mol Dis; 1997 Aug 23; 23(2):288-91. PubMed ID: 9410472
    [Abstract] [Full Text] [Related]

  • 34. Cardiac hemochromatosis in an HFE His63Asp (187C->G) heterozygote.
    Winer D, Silversides C, Israel N, Rinne C, Chang WS, Butany J.
    Can J Cardiol; 2004 Aug 23; 20(10):971-2. PubMed ID: 15332145
    [No Abstract] [Full Text] [Related]

  • 35. Clinical implications of the hemochromatosis gene.
    Tavill AS.
    N Engl J Med; 1999 Sep 02; 341(10):755-7. PubMed ID: 10471465
    [No Abstract] [Full Text] [Related]

  • 36. Population screening for hemochromatosis.
    Adams PC.
    Hepatology; 1999 Apr 02; 29(4):1324-7. PubMed ID: 10094982
    [No Abstract] [Full Text] [Related]

  • 37. No age-related decrease in frequency of heterozygotes for the HFE C282Y haemochromatosis mutation.
    Waalen J, Beutler E.
    J Hepatol; 2004 Jun 02; 40(6):1044; author reply 1044-5. PubMed ID: 15158353
    [No Abstract] [Full Text] [Related]

  • 38. Diagnosis and management of haemochromatosis since the discovery of the HFE gene: a European experience.
    Br J Haematol; 2000 Jan 02; 108(1):31-9. PubMed ID: 10651721
    [No Abstract] [Full Text] [Related]

  • 39. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Gomez PS, Parks S, Ries R, Tran TC, Gomez PF, Press RD.
    Nat Genet; 1999 Nov 02; 23(3):272. PubMed ID: 10545944
    [No Abstract] [Full Text] [Related]

  • 40. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Noll WW, Belloni DR, Stenzel TT, Grody WW.
    Nat Genet; 1999 Nov 02; 23(3):271-2. PubMed ID: 10610176
    [No Abstract] [Full Text] [Related]

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