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    Results: 1 to 20 of 113

    1.

    Prevalence, characteristics, and prognostic significance of HFE gene mutations in type 2 diabetes: the Fremantle Diabetes Study.

    Davis TM, Beilby J, Davis WA, Olynyk JK, Jeffrey GP, Rossi E, Boyder C, Bruce DG.

    Diabetes Care. 2008 Sep;31(9):1795-801. Epub 2008 Jun 19.PMID: 18566337 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Relationships of serum ferritin, transferrin saturation, and HFE mutations and self-reported diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) study.

    Acton RT, Barton JC, Passmore LV, Adams PC, Speechley MR, Dawkins FW, Sholinsky P, Reboussin DM, McLaren GD, Harris EL, Bent TC, Vogt TM, Castro O.

    Diabetes Care. 2006 Sep;29(9):2084-9.PMID: 16936157 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    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

    4.

    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

    5.

    The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic.

    Beutler E, Felitti V, Gelbart T, Ho N.

    Ann Intern Med. 2000 Sep 5;133(5):329-37. Erratum in: Ann Intern Med 2001 Apr 17;134(8):715. PMID: 10979877 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    [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

    7.

    An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy.

    Floreani A, Rosa Rizzotto E, Basso D, Navaglia F, Zaninotto M, Petridis I, DI Andrea O, Testa R, Marra M, Baldo V, Chiaramonte M.

    Aliment Pharmacol Ther. 2007 Aug 15;26(4):577-86.PMID: 17661761 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    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

    9.

    [Mutations in the HFE gene (C282Y, H63D, S65C) in alcoholic patients with finding of iron overload]

    Campos Franco J, González Quintela A, Fernández de Trocóniz LL, Barros Angueira F, Pérez-Quintela BV, Pérez Becerra E, Martínez de Rituerto ST, Otero Antón E, Torre Carballada JA.

    Rev Clin Esp. 2002 Oct;202(10):534-9. Spanish. PMID: 12361551 [PubMed - indexed for MEDLINE]Related articles

    10.

    HFE C282Y homozygotes have reduced low-density lipoprotein cholesterol: the Atherosclerosis Risk in Communities (ARIC) Study.

    Pankow JS, Boerwinkle E, Adams PC, Guallar E, Leiendecker-Foster C, Rogowski J, Eckfeldt JH.

    Transl Res. 2008 Jul;152(1):3-10. Epub 2008 Jun 13.PMID: 18593631 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Clinical expression and insulin sensitivity in type 2 diabetic patients with heterozygous mutations for haemochromatosis.

    Van Lerberghe S, Hermans MP, Dahan K, Buysschaert M.

    Diabetes Metab. 2002 Feb;28(1):33-8.PMID: 11938026 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    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

    13.

    Mild iron overload in patients carrying the HFE S65C gene mutation: a retrospective study in patients with suspected iron overload and healthy controls.

    Holmström P, Marmur J, Eggertsen G, Gåfvels M, Stål P.

    Gut. 2002 Nov;51(5):723-30.PMID: 12377814 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload.

    Cançado RD, Guglielmi AC, Vergueiro CS, Rolim EG, Figueiredo MS, Chiattone CS.

    Sao Paulo Med J. 2006 Mar 2;124(2):55-60.PMID: 16878186 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    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

    16.

    Iron absorption by heterozygous carriers of the HFE C282Y mutation associated with hemochromatosis.

    Hunt JR, Zeng H.

    Am J Clin Nutr. 2004 Oct;80(4):924-31. Erratum in: Am J Clin Nutr. 2005 Mar;81(3):728. PMID: 15447900 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    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

    18.

    Relations among serum ferritin, C282Y and H63D mutations in the HFE gene and type 2 diabetes mellitus in the Czech population.

    Kanková K, Jansen EH, Márová I, Stejskalová A, Pácal L, Muzík J, Vácha J.

    Exp Clin Endocrinol Diabetes. 2002 Aug;110(5):223-9.PMID: 12148086 [PubMed - indexed for MEDLINE]Related articles

    19.

    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

    20.

    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

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