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    Results: 1 to 20 of 738

    1.

    HFE genotype in patients with hemochromatosis and other liver diseases.

    Bacon BR, Olynyk JK, Brunt EM, Britton RS, Wolff RK.

    Ann Intern Med. 1999 Jun 15;130(12):953-62.PMID: 10383365 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    [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. Slovak. PMID: 16871764 [PubMed - indexed for MEDLINE]Related articles

    3.

    Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.

    Sham RL, Ou CY, Cappuccio J, Braggins C, Dunnigan K, Phatak PD.

    Blood Cells Mol Dis. 1997 Aug;23(2):314-20.PMID: 9410475 [PubMed - indexed for MEDLINE]Related articles

    4.

    Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients.

    Phatak PD, Ryan DH, Cappuccio J, Oakes D, Braggins C, Provenzano K, Eberly S, Sham RL.

    Blood Cells Mol Dis. 2002 Jul-Aug;29(1):41-7.PMID: 12482402 [PubMed - indexed for MEDLINE]Related articles

    5.

    Differences in hepatic phenotype between hemochromatosis patients with HFE C282Y homozygosity and other HFE genotypes.

    Cheng R, Barton JC, Morrison ED, Phatak PD, Krawitt EL, Gordon SC, Kowdley KV.

    J Clin Gastroenterol. 2009 Jul;43(6):569-73.PMID: 19359997 [PubMed - indexed for MEDLINE]Related articles

    6.

    HFE mutations, hepatic iron, and fibrosis: ethnic-specific association of NASH with C282Y but not with fibrotic severity.

    Chitturi S, Weltman M, Farrell GC, McDonald D, Kench J, Liddle C, Samarasinghe D, Lin R, Abeygunasekera S, George J.

    Hepatology. 2002 Jul;36(1):142-9. Erratum in: Hepatology 2002 Nov;36(5):1307. PMID: 12085358 [PubMed - indexed for MEDLINE]Related articles

    7.

    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.PMID: 11529872 [PubMed - indexed for MEDLINE]Related articles

    8.

    HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.

    Koefoed P, Dalhoff K, Dissing J, Kramer I, Milman N, Pedersen P, Simonsen K, Tygstrup N, Nielsen FC.

    Scand J Clin Lab Invest. 2002;62(7):527-35.PMID: 12512743 [PubMed - indexed for MEDLINE]Related articles

    9.

    Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.

    Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.

    Eur J Immunogenet. 2000 Jun;27(3):129-34.PMID: 10940080 [PubMed - indexed for MEDLINE]Related articles

    10.

    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.PMID: 9576576 [PubMed - indexed for MEDLINE]Related articles

    11.

    Testing for haemochromatosis in a liver clinic population: relationship between ethnic origin, HFE gene mutations, liver histology and serum iron markers.

    Moodie SJ, Ang L, Stenner JM, Finlayson C, Khotari A, Levin GE, Maxwell JD.

    Eur J Gastroenterol Hepatol. 2002 Mar;14(3):223-9.PMID: 11953685 [PubMed - indexed for MEDLINE]Related articles

    12.

    Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload.

    Porto G, Cardoso CS, Gordeuk V, Cruz E, Fraga J, Areias J, Oliveira JC, Bravo F, Gangaidzo IT, MacPhail AP, Gomo ZA, Moyo VM, Melo G, Silva C, Justiça B, de Sousa M.

    Eur J Haematol. 2001 Aug;67(2):110-8.PMID: 11722599 [PubMed - indexed for MEDLINE]Related articles

    13.

    Hemochromatosis and iron-overload screening in a racially diverse population.

    Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P; Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.

    N Engl J Med. 2005 Apr 28;352(17):1769-78.PMID: 15858186 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.

    Aguilar-Martinez P, Esculié-Coste C, Bismuth M, Giansily-Blaizot M, Larrey D, Schved JF.

    Blood Cells Mol Dis. 2001 Jan-Feb;27(1):290-3.PMID: 11358390 [PubMed - indexed for MEDLINE]Related articles

    15.

    Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.

    Cukjati M, Vaupotic T, Rupreht R, Curin-Serbec V.

    BMC Med Genet. 2007 Nov 23;8:69.PMID: 18036208 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Hereditary hemochromatosis in liver transplantation.

    Fiel MI, Schiano TD, Bodenheimer HC, Thung SN, King TW, Varma CR, Miller CM, Brunt EM, Starnes S, Prass C, Wolff RK, Bacon BR.

    Liver Transpl Surg. 1999 Jan;5(1):50-6.PMID: 9873093 [PubMed - indexed for MEDLINE]Related articles

    17.

    Iron-overload-related disease in HFE hereditary hemochromatosis.

    Allen KJ, Gurrin LC, Constantine CC, Osborne NJ, Delatycki MB, Nicoll AJ, McLaren CE, Bahlo M, Nisselle AE, Vulpe CD, Anderson GJ, Southey MC, Giles GG, English DR, Hopper JL, Olynyk JK, Powell LW, Gertig DM.

    N Engl J Med. 2008 Jan 17;358(3):221-30.PMID: 18199861 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    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.PMID: 14648375 [PubMed - indexed for MEDLINE]Related articles

    19.

    A population-based study of the clinical expression of the hemochromatosis gene.

    Olynyk JK, Cullen DJ, Aquilia S, Rossi E, Summerville L, Powell LW.

    N Engl J Med. 1999 Sep 2;341(10):718-24.PMID: 10471457 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Individuals homozygous for the H63D mutation have significantly elevated iron indexes.

    Samarasena J, Winsor W, Lush R, Duggan P, Xie Y, Borgaonkar M.

    Dig Dis Sci. 2006 Apr;51(4):803-7.PMID: 16615007 [PubMed - indexed for MEDLINE]Related articles

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