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Journal Abstract Search

198 related items for PubMed ID: 9024367

  • 1. Genetic irony beyond haemochromatosis: clinical effects of HLA-H mutations.
    Beutler E.
    Lancet; 1997 Feb 01; 349(9048):296-7. PubMed ID: 9024367
    [No Abstract] [Full Text] [Related]

  • 2. Haemochromatosis... definite maybe!
    Nat Genet; 1996 Aug 01; 13(4):375-6. PubMed ID: 8696321
    [No Abstract] [Full Text] [Related]

  • 3. Haemochromatosis, HFE and genetic complexity.
    Risch N.
    Nat Genet; 1997 Dec 01; 17(4):375-6. PubMed ID: 9398831
    [No Abstract] [Full Text] [Related]

  • 4. 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 01; 14(3):251-2. PubMed ID: 8896550
    [No Abstract] [Full Text] [Related]

  • 5. Haemochromatosis: strike while the iron is hot.
    Cox T.
    Nat Genet; 1996 Aug 01; 13(4):386-8. PubMed ID: 8696327
    [No Abstract] [Full Text] [Related]

  • 6. Two novel polymorphisms (E277K and V212V) in the haemochromatosis gene HFE.
    Bradbury R, Fagan E, Payne SJ.
    Hum Mutat; 2000 Jan 01; 15(1):120. PubMed ID: 10612845
    [No Abstract] [Full Text] [Related]

  • 7. 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 01; 35(10):878-9. PubMed ID: 9783719
    [No Abstract] [Full Text] [Related]

  • 8. Haemochromatosis and HLA-H.
    Jazwinska EC, Cullen LM, Busfield F, Pyper WR, Webb SI, Powell LW, Morris CP, Walsh TP.
    Nat Genet; 1996 Nov 01; 14(3):249-51. PubMed ID: 8896549
    [No Abstract] [Full Text] [Related]

  • 9. Genetic hemochromatosis: why is discovery of the HLA-H gene of interest to rheumatologists?
    Puéchal X.
    Rev Rhum Engl Ed; 1997 Oct 01; 64(10):527-9. PubMed ID: 9385688
    [No Abstract] [Full Text] [Related]

  • 10. [Clinical usefulness of the detection of mutations of the HFE gene in hemochromatosis].
    Oliva R, Sánchez M, Bruguera M, Rodés J.
    Gastroenterol Hepatol; 2000 Nov 01; 23(9):433-5. PubMed ID: 11126040
    [No Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. 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]

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  • 15. 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]

  • 16. [Genetic background and DNA diagnostics of hemochromatosis].
    Heliö T, Färkkilä M, Halme L, Karlsson M, Palotie A, Kontula K.
    Duodecim; 1998 Aug 03; 114(14):1404-9. PubMed ID: 11552248
    [No Abstract] [Full Text] [Related]

  • 17. Hemochromatosis after the gene discovery: revisiting the diagnostic strategy.
    Brissot P, Moirand R, Guyader D, Loréal O, Turlin B, Deugnier Y.
    J Hepatol; 1998 Aug 03; 28 Suppl 1():14-8. PubMed ID: 9575443
    [No Abstract] [Full Text] [Related]

  • 18. [Molecular genetic diagnosis in hemochromatosis].
    Gehrke SG, Stremmel W.
    Dtsch Med Wochenschr; 1999 Apr 09; 124(14):431-4. PubMed ID: 10230385
    [No Abstract] [Full Text] [Related]

  • 19. Haemochromatosis mutation analysis in a normal Irish population.
    Ryan F, Vaughan J.
    Br J Biomed Sci; 2000 Apr 09; 57(4):315-6. PubMed ID: 11204863
    [No Abstract] [Full Text] [Related]

  • 20. [Hereditary hemochromatosis].
    Parkkila S.
    Duodecim; 2000 Apr 09; 116(8):829-36. PubMed ID: 11787126
    [No Abstract] [Full Text] [Related]

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