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Journal Abstract Search

262 related items for PubMed ID: 8896550

  • 1. Haemochromatosis and HLA-H.
    Jouanolle AM, Gandon G, Jézéquel P, Blayau M, Campion ML, Yaouanq J, Mosser J, Fergelot P, Chauvel B, Bouric P, Carn G, Andrieux N, Gicquel I, Le Gall JY, David V.
    Nat Genet; 1996 Nov; 14(3):251-2. PubMed ID: 8896550
    [No Abstract] [Full Text] [Related]

  • 2. Haemochromatosis and HLA-H.
    Jazwinska EC, Cullen LM, Busfield F, Pyper WR, Webb SI, Powell LW, Morris CP, Walsh TP.
    Nat Genet; 1996 Nov; 14(3):249-51. PubMed ID: 8896549
    [No Abstract] [Full Text] [Related]

  • 3. Haemochromatosis, HFE and genetic complexity.
    Risch N.
    Nat Genet; 1997 Dec; 17(4):375-6. PubMed ID: 9398831
    [No Abstract] [Full Text] [Related]

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  • 5. 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 Dec; 9(3):181-6. PubMed ID: 9777338
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  • 6. High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation.
    Tordai A, Andrikovics H, Kalmár L, Rajczy K, Pénzes M, Sarkadi B, Klein I, Váradi A.
    J Med Genet; 1998 Oct; 35(10):878-9. PubMed ID: 9783719
    [No Abstract] [Full Text] [Related]

  • 7. Clinical haemochromatosis in HFE mutation carriers.
    Poullis A, Moodie SJ, Maxwell JD.
    Lancet; 2002 Aug 03; 360(9330):411-2; author reply 413-4. PubMed ID: 12241803
    [No Abstract] [Full Text] [Related]

  • 8. 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 03; 23(3):271. PubMed ID: 10545942
    [No Abstract] [Full Text] [Related]

  • 9. Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis.
    de Villiers JN, Scholtz CL, Hoogendijk CF, Cawood EJ, Kotze MJ.
    Hum Genet; 1998 Jan 03; 102(1):127. PubMed ID: 9490291
    [No Abstract] [Full Text] [Related]

  • 10. Haemochromatosis mutation analysis in a normal Irish population.
    Ryan F, Vaughan J.
    Br J Biomed Sci; 2000 Jan 03; 57(4):315-6. PubMed ID: 11204863
    [No Abstract] [Full Text] [Related]

  • 11. Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?
    Jouanolle AM, Fergelot P, Raoul ML, Gandon G, Roussey M, Deugnier Y, Feingold J, Le Gall JY, David V.
    Ann Genet; 1998 Jan 03; 41(4):195-8. PubMed ID: 9881181
    [Abstract] [Full Text] [Related]

  • 12. Celtic origin of the C282Y mutation of hemochromatosis.
    Lucotte G.
    Blood Cells Mol Dis; 1998 Dec 03; 24(4):433-8. PubMed ID: 9851897
    [Abstract] [Full Text] [Related]

  • 13. Hereditary haemochromatosis mutations (HFE) in patients with Type II diabetes mellitus.
    Braun J, Donner H, Plock K, Rau H, Usadel KH, Badenhoop K.
    Diabetologia; 1998 Aug 03; 41(8):983-4. PubMed ID: 9726605
    [No Abstract] [Full Text] [Related]

  • 14. Genetic hemochromatosis: why is discovery of the HLA-H gene of interest to rheumatologists?
    Puéchal X.
    Rev Rhum Engl Ed; 1997 Oct 03; 64(10):527-9. PubMed ID: 9385688
    [No Abstract] [Full Text] [Related]

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  • 17. [Hereditary hemochromatosis].
    Parkkila S.
    Duodecim; 2000 Oct 03; 116(8):829-36. PubMed ID: 11787126
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  • 19. 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
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  • 20. Role of C282Y mutation in haemochromatosis gene in development of type 2 diabetes in healthy men: prospective cohort study.
    Salonen JT, Tuomainen TP, Kontula K.
    BMJ; 2000 Jun 24; 320(7251):1706-7. PubMed ID: 10864547
    [No Abstract] [Full Text] [Related]

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