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    Results: 1 to 20 of 273

    1.

    Screening for hereditary hemochromatosis in siblings and children of affected patients. A cost-effectiveness analysis.

    El-Serag HB, Inadomi JM, Kowdley KV.

    Ann Intern Med. 2000 Feb 15;132(4):261-9.PMID: 10681280 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.

    Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT.

    Blood Cells Mol Dis. 1999 Jun-Aug;25(3-4):147-55.PMID: 10575540 [PubMed - indexed for MEDLINE]Related articles

    3.

    [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland]

    Himmelmann A, Bortoluzzi L, Jansen S, Fehr J.

    Schweiz Med Wochenschr. 2000 Aug 8;130(31-32):1112-9. German. PMID: 11008304 [PubMed - indexed for MEDLINE]Related articles

    4.

    [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

    5.

    [Screening for hereditary HFE hemochromatosis]

    Deugnier Y, Jouanolle AM.

    Presse Med. 2007 Sep;36(9 Pt 2):1292-4. Epub 2007 Jun 4. French. PMID: 17544612 [PubMed - indexed for MEDLINE]Related articles

    6.

    Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.

    Hellerbrand C, Bosserhoff AK, Seegers S, Lingner G, Wrede C, Lock G, Schölmerich J, Büttner R.

    Scand J Gastroenterol. 2001 Nov;36(11):1211-6.PMID: 11686223 [PubMed - indexed for MEDLINE]Related articles

    7.

    Update on hereditary hemochromatosis and the HFE gene.

    Brandhagen DJ, Fairbanks VF, Batts KP, Thibodeau SN.

    Mayo Clin Proc. 1999 Sep;74(9):917-21. Review.PMID: 10488796 [PubMed - indexed for MEDLINE]Related articles

    8.

    Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.

    Bittencourt PL, Palácios SA, Couto CA, Cançado EL, Carrilho FJ, Laudanna AA, Kalil J, Gayotto LC, Goldberg AC.

    Braz J Med Biol Res. 2002 Mar;35(3):329-35.PMID: 11887210 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    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

    10.

    Nonexpressing homozygotes for C282Y hemochromatosis: minority or majority of cases?

    Adams PC.

    Mol Genet Metab. 2000 Sep-Oct;71(1-2):81-6. Review.PMID: 11001800 [PubMed - indexed for MEDLINE]Related articles

    11.

    Genetic testing for HFE hemochromatosis in Australia: the value of testing relatives of simple heterozygotes.

    Cavanaugh JA, Wilson SR, Bassett ML.

    J Gastroenterol Hepatol. 2002 Jul;17(7):800-3.PMID: 12121511 [PubMed - indexed for MEDLINE]Related articles

    12.

    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.PMID: 11875012 [PubMed - indexed for MEDLINE]Related articles

    13.

    Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene.

    Pietrangelo A, Montosi G, Totaro A, Garuti C, Conte D, Cassanelli S, Fraquelli M, Sardini C, Vasta F, Gasparini P.

    N Engl J Med. 1999 Sep 2;341(10):725-32.PMID: 10471458 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    A primer for predicting risk of disease in HFE-linked hemochromatosis.

    Adams PC, Walker AP, Acton RT.

    Genet Test. 2001 Winter;5(4):311-6.PMID: 11960576 [PubMed - indexed for MEDLINE]Related articles

    15.

    Screening blood donors for hereditary hemochromatosis: decision analysis model based on a 30-year database.

    Adams PC, Gregor JC, Kertesz AE, Valberg LS.

    Gastroenterology. 1995 Jul;109(1):177-88.PMID: 7797016 [PubMed - indexed for MEDLINE]Related articles

    16.

    A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.

    Jouanolle AM, Fergelot P, Gandon G, Yaouanq J, Le Gall JY, David V.

    Hum Genet. 1997 Oct;100(5-6):544-7.PMID: 9341868 [PubMed - indexed for MEDLINE]Related articles

    17.

    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

    18.

    Screening blood donors for hereditary hemochromatosis: decision analysis model comparing genotyping to phenotyping.

    Adams PC, Valberg LS.

    Am J Gastroenterol. 1999 Jun;94(6):1593-600.PMID: 10364030 [PubMed - indexed for MEDLINE]Related articles

    19.

    Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?

    Cadet E, Capron D, Gallet M, Omanga-Léké ML, Boutignon H, Julier C, Robson KJ, Rochette J.

    J Med Genet. 2005 May;42(5):390-5.PMID: 15863667 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Cost-effectiveness of microsatellite instability screening as a method for detecting hereditary nonpolyposis colorectal cancer.

    Ramsey SD, Clarke L, Etzioni R, Higashi M, Berry K, Urban N.

    Ann Intern Med. 2001 Oct 16;135(8 Pt 1):577-88.PMID: 11601929 [PubMed - indexed for MEDLINE]Related articlesFree article

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