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Journal Abstract Search

135 related items for PubMed ID: 11903354

  • 21. The role of hemochromatosis susceptibility gene mutations in protecting against iron deficiency in celiac disease.
    Butterworth JR, Cooper BT, Rosenberg WM, Purkiss M, Jobson S, Hathaway M, Briggs D, Howell WM, Wood GM, Adams DH, Iqbal TH.
    Gastroenterology; 2002 Aug; 123(2):444-9. PubMed ID: 12145797
    [Abstract] [Full Text] [Related]

  • 22. HFE mutations, iron deficiency and overload in 10,500 blood donors.
    Jackson HA, Carter K, Darke C, Guttridge MG, Ravine D, Hutton RD, Napier JA, Worwood M.
    Br J Haematol; 2001 Aug; 114(2):474-84. PubMed ID: 11529872
    [Abstract] [Full Text] [Related]

  • 23. 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; 26(3):229-33. PubMed ID: 10950943
    [Abstract] [Full Text] [Related]

  • 24. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.
    Vnitr Lek; 2006 Jun; 52(6):602-8. PubMed ID: 16871764
    [Abstract] [Full Text] [Related]

  • 25. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
    Byrnes V, Ryan E, O'Keane C, Crowe J.
    Blood Cells Mol Dis; 2000 Feb; 26(1):2-8. PubMed ID: 10772870
    [Abstract] [Full Text] [Related]

  • 26. A homozygous HFE gene splice site mutation (IVS5+1 G/A) in a hereditary hemochromatosis patient of Vietnamese origin.
    Steiner M, Ocran K, Genschel J, Meier P, Gerl H, Ventz M, Schneider ML, Büttner C, Wadowska K, Kerner W, Schuff-Werner P, Lochs H, Schmidt H.
    Gastroenterology; 2002 Mar; 122(3):789-95. PubMed ID: 11875012
    [Abstract] [Full Text] [Related]

  • 27. HFE mutations do not account for transfusional iron overload in patients with acute myeloid leukemia.
    Parkkila S, Niemelä O, Savolainen ER, Koistinen P.
    Transfusion; 2001 Jun; 41(6):828-31. PubMed ID: 11399828
    [Abstract] [Full Text] [Related]

  • 28. Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC.
    Le Gac G, Mura C, Férec C.
    Clin Chem; 2001 Sep; 47(9):1633-40. PubMed ID: 11514397
    [Abstract] [Full Text] [Related]

  • 29. Reference centiles for serum ferritin and percentage of transferrin saturation, with application to mutations of the HFE gene.
    Koziol JA, Ho NJ, Felitti VJ, Beutler E.
    Clin Chem; 2001 Oct; 47(10):1804-10. PubMed ID: 11568090
    [Abstract] [Full Text] [Related]

  • 30. Mutations in the HFE gene and their interaction with exogenous risk factors in hepatocellular carcinoma.
    Fargion S, Stazi MA, Fracanzani AL, Mattioli M, Sampietro M, Tavazzi D, Bertelli C, Patriarca V, Mariani C, Fiorelli G.
    Blood Cells Mol Dis; 2001 Oct; 27(2):505-11. PubMed ID: 11500061
    [Abstract] [Full Text] [Related]

  • 31. Hemochromatosis with HFE gene mutation in a Japanese patient.
    Sohda T, Okubo R, Kamimura S, Ohkawara T.
    Am J Gastroenterol; 2001 Aug; 96(8):2487-8. PubMed ID: 11513196
    [Abstract] [Full Text] [Related]

  • 32. Compound heterozygotes for hemochromatosis gene mutations: may they help to understand the pathophysiology of the disease?
    Aguilar Martinez P, Biron C, Blanc F, Masmejean C, Jeanjean P, Michel H, Schved JF.
    Blood Cells Mol Dis; 1997 Aug; 23(2):269-76. PubMed ID: 9410470
    [Abstract] [Full Text] [Related]

  • 33. Hepatic iron overload: direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis.
    Press RD, Flora K, Gross C, Rabkin JM, Corless CL.
    Am J Clin Pathol; 1998 May; 109(5):577-84. PubMed ID: 9576576
    [Abstract] [Full Text] [Related]

  • 34. Mutations of the HFE gene among Turkish hereditary hemochromatosis patients.
    Simsek H, Balaban YH, Yilmaz E, Sumer H, Buyukasik Y, Cengiz C, Ozcebe O, Hascelik G, Tatar G.
    Ann Hematol; 2005 Oct; 84(10):646-9. PubMed ID: 15871018
    [Abstract] [Full Text] [Related]

  • 35. A primer for predicting risk of disease in HFE-linked hemochromatosis.
    Adams PC, Walker AP, Acton RT.
    Genet Test; 2001 Oct; 5(4):311-6. PubMed ID: 11960576
    [Abstract] [Full Text] [Related]

  • 36. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes.
    Raddatz D, Legler T, Lynen R, Addicks N, Ramadori G.
    Z Gastroenterol; 2003 Nov; 41(11):1069-76. PubMed ID: 14648375
    [Abstract] [Full Text] [Related]

  • 37. HFE-associated hereditary hemochromatosis.
    Eijkelkamp EJ, Yapp TR, Powell LW.
    Can J Gastroenterol; 2000 Feb; 14(2):121-5. PubMed ID: 10694284
    [Abstract] [Full Text] [Related]

  • 38. Hereditary hemochromatosis in Spain.
    Sánchez M, Bruguera M, Quintero E, Barrio Y, Mazzara R, Rodés J, Oliva R.
    Genet Test; 2000 Feb; 4(2):171-6. PubMed ID: 10953957
    [Abstract] [Full Text] [Related]

  • 39. Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells.
    Waheed A, Parkkila S, Zhou XY, Tomatsu S, Tsuchihashi Z, Feder JN, Schatzman RC, Britton RS, Bacon BR, Sly WS.
    Proc Natl Acad Sci U S A; 1997 Nov 11; 94(23):12384-9. PubMed ID: 9356458
    [Abstract] [Full Text] [Related]

  • 40. The C282Y mutation causing hereditary hemochromatosis does not produce a null allele.
    Levy JE, Montross LK, Cohen DE, Fleming MD, Andrews NC.
    Blood; 1999 Jul 01; 94(1):9-11. PubMed ID: 10381492
    [Abstract] [Full Text] [Related]

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