BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 15990686)

  • 1. Hemochromatosis-causing mutations C282Y and H63D are not risk factors for atherothrombotic cerebral infarction.
    Hruskovicová H; Milanez T; Kobal J; Potisk KP; Petrovic D; Peterlin B
    Med Sci Monit; 2005 Jul; 11(7):BR248-52. PubMed ID: 15990686
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Population-based study of the relationship between mutations in the hemochromatosis (HFE) gene and arthritis.
    Sherrington CA; Knuiman MW; Divitini ML; Bartholomew HC; Cullen DJ; Olynyk JK
    J Gastroenterol Hepatol; 2006 Mar; 21(3):595-8. PubMed ID: 16638105
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary hemochromatosis and risk of ischemic heart disease: a prospective study and a case-control study.
    Ellervik C; Tybjaerg-Hansen A; Grande P; Appleyard M; Nordestgaard BG
    Circulation; 2005 Jul; 112(2):185-93. PubMed ID: 15998685
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hemochromatosis gene mutations, liver function tests and iron status in alcohol-dependent patients admitted for detoxification.
    Robinson G; Narasimhan S; Weatherall M; Beasley R
    J Gastroenterol Hepatol; 2007 Jun; 22(6):852-4. PubMed ID: 17565641
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.
    Pedersen P; Milman N
    Ann Hematol; 2009 Aug; 88(8):775-84. PubMed ID: 19159930
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary hemochromatosis genotypes and risk of ischemic stroke.
    Ellervik C; Tybjaerg-Hansen A; Appleyard M; Sillesen H; Boysen G; Nordestgaard BG
    Neurology; 2007 Mar; 68(13):1025-31. PubMed ID: 17389307
    [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. Haemochromatosis-causing mutations C282Y and H63D are not risk factors for coronary artery disease in Caucasians with type 2 diabetes.
    Zorc M; Hruskovicová H; Petrovic MG; Milcić M; Peterlin B; Petrovic D
    Folia Biol (Praha); 2004; 50(2):69-70. PubMed ID: 15222129
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic risk for atherothrombotic cerebral infarction in individuals stratified by sex or conventional risk factors for atherosclerosis.
    Yamaguchi S; Yamada Y; Metoki N; Yoshida H; Satoh K; Ichihara S; Kato K; Kameyama T; Yokoi K; Matsuo H; Segawa T; Watanabe S; Nozawa Y
    Int J Mol Med; 2006 Nov; 18(5):871-83. PubMed ID: 17016617
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Are the hemochromatosis (HFE) gene mutation and hepatitis C virus (HCV) infection risk factors for porphyria cutanea tarda?].
    Nagy Z; Kószó F; Pár A; Nagy A; Horányi M; Morvay M; Dobozy A; Mózsik G
    Orv Hetil; 2000 Sep; 141(37):2031-4. PubMed ID: 11037612
    [TBL] [Abstract][Full Text] [Related]  

  • 11. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload?
    de Diego C; Opazo S; Murga MJ; Martínez-Castro P
    Eur J Haematol; 2007 Jan; 78(1):66-71. PubMed ID: 17042772
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration.
    Zamboni P; Tognazzo S; Izzo M; Pancaldi F; Scapoli GL; Liboni A; Gemmati D
    J Vasc Surg; 2005 Aug; 42(2):309-14. PubMed ID: 16102632
    [TBL] [Abstract][Full Text] [Related]  

  • 13. HFE mutations and risk of coronary heart disease in middle-aged women.
    van der A DL; Peeters PH; Grobbee DE; Roest M; Marx JJ; Voorbij HM; van der Schouw YT
    Eur J Clin Invest; 2006 Oct; 36(10):682-90. PubMed ID: 16968463
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hemochromatosis-associated gene mutations in patients with myelodysplastic syndromes with refractory anemia with ringed sideroblasts.
    Nearman ZP; Szpurka H; Serio B; Warshawksy I; Theil K; Lichtin A; Sekeres MA; Maciejewski JP
    Am J Hematol; 2007 Dec; 82(12):1076-9. PubMed ID: 17654685
    [TBL] [Abstract][Full Text] [Related]  

  • 15. C282Y and H63D mutations of the haemochromatosis gene in patients with iron overload.
    Jorquera F; Domínguez A; Díaz-Golpe V; Espinel J; Muñoz F; Herrera A; Fernández-Gundín MJ; Vivas S; Olcoz JL
    Rev Esp Enferm Dig; 2001 May; 93(5):293-302. PubMed ID: 11488107
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hemochromatosis gene mutations and distal adenomatous colorectal polyps.
    McGlynn KA; Sakoda LC; Hu Y; Schoen RE; Bresalier RS; Yeager M; Chanock S; Hayes RB; Buetow KH
    Cancer Epidemiol Biomarkers Prev; 2005 Jan; 14(1):158-63. PubMed ID: 15668490
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unique genetic profile of hereditary hemochromatosis in Russians: high frequency of C282Y mutation in population, but not in patients.
    Potekhina ES; Lavrov AV; Samokhodskaya LM; Efimenko AY; Balatskiy AV; Baev AA; Litvinova MM; Nikitina LA; Shipulin GA; Bochkov NP; Tkachuk VA; Bochkov VN
    Blood Cells Mol Dis; 2005; 35(2):182-8. PubMed ID: 16055358
    [TBL] [Abstract][Full Text] [Related]  

  • 18. HFE genotypes and dietary heme iron: no evidence of strong gene-nutrient interaction on serum ferritin concentrations in middle-aged women.
    van der A DL; Peeters PH; Grobbee DE; Roest M; Voorbij HA; van der Schouw YT
    Nutr Metab Cardiovasc Dis; 2006 Jan; 16(1):60-8. PubMed ID: 16399493
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A rare case of a patient heterozygous for the hemochromatosis mutation C282Y and homozygous for H63D.
    Lucotte G; Champenois T; Sémonin O
    Blood Cells Mol Dis; 2001; 27(5):892-3. PubMed ID: 11783952
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Survival after liver transplantation in patients with hepatic iron overload: the national hemochromatosis transplant registry.
    Kowdley KV; Brandhagen DJ; Gish RG; Bass NM; Weinstein J; Schilsky ML; Fontana RJ; McCashland T; Cotler SJ; Bacon BR; Keeffe EB; Gordon F; Polissar N;
    Gastroenterology; 2005 Aug; 129(2):494-503. PubMed ID: 16083706
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.