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Journal Abstract Search

198 related items for PubMed ID: 9024367

  • 21. Hereditary hemochromatosis: a HpaI polymorphism within the HLA-H gene.
    Totaro A, Grifa A, Carella M, D'Ambrosio L, Valentino M, Roth MP, Borot N, Coppin H, Roetto A, Camaschella C, Gasparini P.
    Mol Cell Probes; 1997 Jun; 11(3):229-30. PubMed ID: 9232622
    [No Abstract] [Full Text] [Related]

  • 22. Traffic jam for hemochromatosis mutant protein.
    Adams PC.
    Hepatology; 1997 Dec; 26(6):1684-5. PubMed ID: 9398018
    [No Abstract] [Full Text] [Related]

  • 23. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium.
    Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJ, Jouanolle AM, Mosser A, David V, Le Gall JY, Halsall DJ, Elsey TS, Kelly A, Cox TM, Clare M, Bomford A, Vandwalle JL, Rochette J, Borot N, Coppin H, Roth MP, Ryan E, Crowe J, Totaro A, Gasparini P, Roetto A, Walker AP.
    Nat Genet; 1999 Nov; 23(3):271. PubMed ID: 10545942
    [No Abstract] [Full Text] [Related]

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

  • 25.
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  • 26. Mutation analysis of the HLA-H gene in French hemochromatosis patients, and genetic counseling in families.
    Mercier G, Burckel A, Bathelier C, Boillat E, Lucotte G.
    Genet Couns; 1998 Sep; 9(3):181-6. PubMed ID: 9777338
    [Abstract] [Full Text] [Related]

  • 27. 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]

  • 28. [Hereditary hemochromatosis: biochemical and genetic diagnosis].
    Quintero E.
    Gastroenterol Hepatol; 1999 Feb; 22 Suppl 1():1-5. PubMed ID: 10085593
    [No Abstract] [Full Text] [Related]

  • 29. HLA-H and associated proteins in patients with hemochromatosis.
    Beutler E, West C, Gelbart T.
    Mol Med; 1997 Jun; 3(6):397-402. PubMed ID: 9234244
    [Abstract] [Full Text] [Related]

  • 30. [Detection of HFE polymorphism in German patients with hereditary hemochromatosis].
    Burggraf S, Olgemöller B.
    Dtsch Med Wochenschr; 2000 Nov 03; 125(44):1346; author reply 1347. PubMed ID: 11109419
    [No Abstract] [Full Text] [Related]

  • 31. Molecular analysis of HLA-H gene mutations in New Zealand patients with haemochromatosis.
    Burt MJ, Upton JD, Morison IM, Chapman BA, Faed JM, George PM.
    N Z Med J; 1997 Nov 28; 110(1056):429-32. PubMed ID: 9418837
    [Abstract] [Full Text] [Related]

  • 32. Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis.
    Jeffrey GP, Chakrabarti S, Hegele RA, Adams PC.
    Nat Genet; 1999 Aug 28; 22(4):325-6. PubMed ID: 10431233
    [No Abstract] [Full Text] [Related]

  • 33. Haemochromatosis case detection by genetic testing: a new era.
    Kilpatrick ES, Jagger C.
    Ann Clin Biochem; 1998 Sep 28; 35 ( Pt 5)():674-7. PubMed ID: 9768336
    [No Abstract] [Full Text] [Related]

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  • 35. 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 28; 23(2):288-91. PubMed ID: 9410472
    [Abstract] [Full Text] [Related]

  • 36. 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 28; 23(3):272. PubMed ID: 10545944
    [No Abstract] [Full Text] [Related]

  • 37. 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]

  • 38. 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]

  • 39. 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]

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

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