BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

93 related articles for article (PubMed ID: 11684826)

  • 1. Risk of disease in siblings of patients with hereditary hemochromatosis.
    Nelson RL; Persky V; Davis F; Becker E
    Digestion; 2001; 64(2):120-4. PubMed ID: 11684826
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Risk of neoplastic and other diseases among people with heterozygosity for hereditary hemochromatosis.
    Nelson RL; Davis FG; Persky V; Becker E
    Cancer; 1995 Sep; 76(5):875-9. PubMed ID: 8625192
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Is hereditary hemochromatosis a balanced polymorphism: an analysis of family size among hemochromatosis heterozygotes.
    Nelson RL; Persky V; Davis F; Becker E
    Hepatogastroenterology; 2001; 48(38):523-6. PubMed ID: 11379346
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 16871764
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Effect of C282Y genotype on self-reported musculoskeletal complications in hereditary hemochromatosis.
    Camacho A; Funck-Brentano T; Simão M; Cancela L; Ottaviani S; Cohen-Solal M; Richette P
    PLoS One; 2015; 10(3):e0122817. PubMed ID: 25822977
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.
    Lawless MW; White M; Mankan AK; O'Dwyer MJ; Norris S
    Tissue Antigens; 2007 Oct; 70(4):294-300. PubMed ID: 17767550
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Searching for hereditary hemochromatosis.
    Laudicina RJ
    Clin Lab Sci; 2006; 19(3):174-83. PubMed ID: 16910235
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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. PubMed ID: 15863667
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
    Martinelli AL; Filho R; Cruz S; Franco R; Tavella M; Secaf M; Ramalho L; Zucoloto S; Rodrigues S; Zago M
    Genet Mol Res; 2005 Mar; 4(1):31-8. PubMed ID: 15841433
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Insurance, employment, and psychosocial consequences of a diagnosis of hereditary hemochromatosis in subjects without end organ damage.
    Shaheen NJ; Lawrence LB; Bacon BR; Barton JC; Barton NH; Galanko J; Martin CF; Burnett CK; Sandler RS
    Am J Gastroenterol; 2003 May; 98(5):1175-80. PubMed ID: 12809845
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Increased mortality risk in patients with phenotypic hereditary hemochromatosis but not in their first-degree relatives.
    Elmberg M; Hultcrantz R; Ebrahim F; Olsson S; Lindgren S; Lööf L; Stål P; Wallerstedt S; Almer S; Sandberg-Gertzén H; Ekbom A; Askling J
    Gastroenterology; 2009 Oct; 137(4):1301-9. PubMed ID: 19622361
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical characteristics of hereditary hemochromatosis patients who lack the C282Y mutation.
    Shaheen NJ; Bacon BR; Grimm IS
    Hepatology; 1998 Aug; 28(2):526-9. PubMed ID: 9696020
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Morbidity and mortality in first-degree relatives of C282Y homozygous probands with clinically detected haemochromatosis compared with the general population: the HEmochromatosis FAmily Study (HEFAS).
    Jacobs EM; Hendriks JC; Marx JJ; van Deursen CT; Kreeftenberg HG; de Vries RA; Stalenhoef AF; Verbeek AL; Swinkels DW
    Neth J Med; 2007 Dec; 65(11):425-33. PubMed ID: 18079565
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Family-based detection for hereditary hemochromatosis.
    Reyes M; Dunet DO; Isenberg KB; Trisolini M; Wagener DK
    J Genet Couns; 2008 Feb; 17(1):92-100. PubMed ID: 17952576
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary hemochromatosis.
    Fix OK; Kowdley KV
    Minerva Med; 2008 Dec; 99(6):605-17. PubMed ID: 19034258
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary hemochromatosis is characterized by a clinically definable arthropathy that correlates with iron load.
    Carroll GJ; Breidahl WH; Bulsara MK; Olynyk JK
    Arthritis Rheum; 2011 Jan; 63(1):286-94. PubMed ID: 20954257
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Predictive value of family history in diagnosis of hereditary hemochromatosis.
    Assy N; Adams PC
    Dig Dis Sci; 1997 Jun; 42(6):1312-5. PubMed ID: 9201100
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis.
    Stickel F; Buch S; Zoller H; Hultcrantz R; Gallati S; Österreicher C; Finkenstedt A; Stadlmayr A; Aigner E; Sahinbegovic E; Sarrazin C; Schafmayer C; Braun F; Erhart W; Nothnagel M; Lerch MM; Mayerle J; Völzke H; Schaller A; Kratzer W; Boehm BO; Sipos B; D'Amato M; Torkvist L; Stal P; Arlt A; Franke A; Becker T; Krawczak M; Zwerina J; Berg T; Hinrichsen H; Krones E; Dejaco C; Strasser M; Datz C; Hampe J
    Hum Mol Genet; 2014 Jul; 23(14):3883-90. PubMed ID: 24556216
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Screening for C282Y homozygosity in a Norwegian population (HUNT2): The sensitivity and specificity of transferrin saturation.
    Thorstensen K; Kvitland MA; Irgens WØ; Hveem K; Asberg A
    Scand J Clin Lab Invest; 2010 Apr; 70(2):92-7. PubMed ID: 20073670
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pathogenesis of hereditary hemochromatosis: genetics and beyond.
    Britton RS; Fleming RE; Parkkila S; Waheed A; Sly WS; Bacon BR
    Semin Gastrointest Dis; 2002 Apr; 13(2):68-79. PubMed ID: 12064862
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.